2.1 Historically, Immunity Has Been Understood As the Capacity of an Organism to Defend Itself against Pathogens

Pathogens have constituted a major force shaping the evolution of human beings throughout their history. Devastating infectious diseases are a clear example. Plague, caused by the bacterium Yersinia pestis, killed more than 50 million people in the fourteenth century. More recently, the pandemic of influenza virus following the First World War killed over 40 million people worldwide.

It has long been recognized that humans can resist some infections, with important differences between individuals and/or populations. While some people are killed, others show disease symptoms but survive, and still others do not seem to be affected at all. The notion of immunity is meant to capture this idea of a specific capacity to avoid the detrimental effects of a pathogen. Immunity is generally defined as the capacity by which an organism can defend itself against pathogens.

Host–pathogen interactions are complex, as each partner adapts to the other. This emphasizes the need to always understand immune defense and pathogenicity in their ecological and evolutionary contexts (Box 2.2).

Historically, the definition of immunity as defense against pathogens is intimately connected with the development of the vaccination technique (Reference MoulinMoulin 1991; Reference SilversteinSilverstein 2009). The birth of immunology as a biomedical field was related with the process of so-called immunization, that is, the acquisition of protection against a specific agent. Etymologically, immunity means an exemption (the right to legally escape specific taxes in ancient Rome). The development of large-scale scientific vaccinations, particularly with Robert Koch and Louis Pasteur in the nineteenth century, is often seen as one of the main foundations of the field of immunology (Reference BazinBazin 2011). Vaccination is connected with the idea that an organism can increase its defense capacity by “learning” how to neutralize a given pathogen. The vaccinated organism responds quicker and more strongly if it reenters into contact with the same pathogen. This capacity is called immunological memory, a phenomenon that has long been used to make a distinction between two arms of immunity, namely innate and adaptive immunity (Box 2.3).

2.2 Defensive Immune Mechanisms Have Been Identified in Virtually All Living Things

Beyond humans, all animals, plants, unicellular eukaryotes, bacteria, and archaea are constantly under the potential threat of pathogens and have evolved multiple mechanisms to cope with those pathogens (Reference Anderson and MayAnderson and May 1982; Reference Stearns and KoellaStearns and Koella 2008). Contrary to the long-held view that only vertebrates possess an immune system, in the last thirty years or so immune systems have been found in all the species in which their presence has been thoroughly investigated (Reference PradeuPradeu 2012). Importantly, one can observe that, in all these cases, the criterion used for saying that an immune system exists in a species has been the identification of a system of recognition, control, and elimination of pathogens. This confirms that defense remains the intrinsic, if sometimes implicit, definition of immunity that most biologists adopt when they talk about the immune system.

Plants lack a circulatory system and mobile immune cells, but they are capable of establishing immune responses that are highly specific, with limited damage to the host, and that can even generate a form of immunological memory (Reference Spoel and DongSpoel and Dong 2012). Plants deal with pathogens by diverse modes of recognition (including nucleotide-binding domain, leucine-rich repeat (NLR) receptors) and effector responses (Reference Jones and DanglJones and Dangl 2006).

Bacteria and archaea can be infected by pathogens, including viruses called bacteriophages, or more simply phages. They respond to these pathogens through different immune mechanisms, including suppression of phage adsorption, restriction modification of the invading phage genome, abortive infection, and the recently discovered CRISPR-Cas systems (CRISPR stands for “Clustered, Regularly Interspaced, Short Palindromic Repeats”) (Reference Hille, Richter and WongHille et al. 2018). CRISPR-Cas systems provide many bacteria and archaea with protection against phages and other mobile elements (including plasmids and transposons) through a three-step process. The first step is adaptation: small fragments of DNA from the invader are incorporated into the CRISPR array of the host. The second step is expression and processing: the CRISPR array is transcribed, and the precursor transcript is processed to generate CRISPR RNAs. The final step is interference: the CRISPR RNA guides a complex of Cas proteins to the matching target, which initiates the destruction of the invading nucleic acid (Reference Jackson, McKenzie and FagerlundJackson et al. 2017). CRISPR-Cas has generally been described as a key defense mechanism of prokaryotes against mobile elements (including phages) (Reference Horvath and BarrangouHorvath and Barrangou 2010), along with other, more recently identified antiphage defense systems (Reference Doron, Melamed and OfirDoron et al. 2018). Most experts even consider CRISPR-Cas as a form of adaptive immunity in bacteria and archaea (because it displays a form of immunological memory) on top of being heritable, as it can be transmitted to daughter cells (Reference Horvath and BarrangouHorvath and Barrangou 2010; Reference Hille, Richter and WongHille et al. 2018). This has led to discussions over the potentially Lamarckian nature of the CRISPR-Cas system (see (Reference KooninKoonin 2019) and accompanying commentaries).

Other important examples of organisms with now well-described immune systems include insects (Reference Lemaitre and HoffmannLemaitre and Hoffmann 2007), sponges, hydra, and slime molds (Reference MüllerMüller 2003; Reference Chen, Zhuchenko and KuspaChen et al. 2007; Reference Augustin, Fraune and BoschAugustin et al. 2010).

2.3 Extended Immunity: Immunity Goes Well Beyond Defense

The centrality of host defense against pathogens in the survival of all organisms should not obscure the fact that immunity goes well beyond mere defense. Although immunity was long conceived exclusively as a system of defense, recent research has shown that immune processes actually play a critical role in a wide variety of physiological phenomena such as development, tissue repair, clearance of debris or dead cells, maintenance of local tissue functions, metabolism, thermogenesis, and the functioning of the nervous system, among many others (Reference PradeuPradeu 2012; Reference Rankin and ArtisRankin and Artis 2018), leading to an extended view of immunity. Repair is a particularly fundamental process, which maintains the integrity and cohesion of the organism. When you cut yourself, in addition to the well-known action of platelets, which initiate blood clot and vasculature closure, a horde of immune cells is required at every stage of the repair process to insure proper wound healing (Reference Gurtner, Werner, Barrandon and LongakerGurtner et al. 2008; Reference Wynn and VannellaWynn and Vannella 2016). The three key stages are inflammation, new tissue formation, and remodeling. The main immune cells participating in tissue repair are neutrophils and macrophages. The plasticity and adaptation to context of these cells are crucial (Reference Laurent, Jolivel and ManickiLaurent et al. 2017). Immune cells are also important in processes of regeneration, such as those found in plants, hydra, arthropods, and amphibians, and by which entire complex structures such as limbs can regrow (Reference Eming, Martin and Tomic-CanicEming et al. 2014). Another key daily activity of the immune system is the clearance of bodily debris, coordinated by phagocytotic cells (Reference NagataNagata 2018). In addition, the immune system is essential for development, that is, the early construction of the organism. This includes the indispensable role of immune-mediated apoptosis and phagocytosis very early on in many developmental processes (Reference Wynn, Chawla and PollardWynn et al. 2013; Reference Okabe and MedzhitovOkabe and Medzhitov 2016), as well as the role of the complement in development (Reference Ricklin, Hajishengallis, Yang and LambrisRicklin et al. 2010; Reference Stephan, Barres and StevensStephan et al. 2012) (e.g., phagocytosis mediates the indispensable elimination of excessive tissues; the complement, a cascade of proteins in the blood, remodels synaptic connections in the developing nervous system). Importantly, even though the above description applies mainly to animals, the observation that the immune system realizes various activities beyond defense holds across all living organisms; for example, CRISPR-Cas systems in prokaryotes participate not only in defense but also in repair.

Many of the same actors that ensure the defense of the organism against pathogens, therefore, are equally central for processes previously considered as nonimmune and which overlap to a significant degree (Figure 2.2). Perhaps one could even consider that the very division of these processes into such categories as “defense,” “repair,” and “development” reflects more the way we, as investigators, address questions about bodily systems (and divide such processes into convenient categories) than real differences in nature. From this point of view, there would be much to say in favor of a revised epistemology of immunology, understood as a reflection on how the categories by which the immune system has been conceived (in the context of the division into systems) could be redefined and redrawn.

Figure 2.2

Extended immunity: overview of the various, partly overlapping, activities of the immune system. The immune system not only defends the organism against different potential threats but also constructs, repairs, cleans up the organism, and maintains tissue homeostasis, among other activities.

2.4 Accounting for the Evolution of Immunological Processes and Attributing a Function to the Immune System Have Become Difficult

The extension of immunity well beyond defense has consequences for two central issues, namely the evolutionary history of immune systems and functional ascription in the case of the immune system. It increasingly appears that immune systems have evolved under different selective pressures, which include the necessity to defend the organism against pathogens but are much more diverse than that. Natural selection has favored immune systems efficient at simultaneously defending, constructing, repairing, cleaning up, and maintaining the organism. Many trade-offs exist among these various selective pressures. For example, so-called type 2 immunity (essential for repair, but also in response to parasites) is partly at odds with type 1 immunity (which responds to intracellular abnormalities, including viruses and intracellular bacteria), as the activation of one weakens the efficacy of the other. Current immune systems function by balancing these different dimensions and reaching a complex equilibrium between them in the context of present and past environmental pressures (Reference EberlEberl 2016).

This discussion also brings up the question of the origins of the first immune systems. The capacity to regulate the various processes of defense, development, repair, clearance of debris, and maintenance of homeostasis is probably as ancient as life itself. If so, then all living things that currently exist or have existed in the past have an immune system. The key question, therefore, becomes how replicating molecules started to acquire, a few billions of years ago, the capacity to coalesce into groups, stick together, and maintain, repair, and defend themselves at this emerging group level. Much later, the same question was raised for the transition from unicellular to multicellular organisms where, again, the constitution of an immune system at the multicellular level was crucial (Reference MichodMichod 1999; Reference Pradeu, Bouchard and HunemanPradeu 2013). Obviously, this approach to the evolution of immune systems is entirely different from the classic (and naturally important) discussion in immunology over how adaptive immune systems evolved in vertebrates some 400 to 500 million years ago (Reference Pancer and CooperPancer and Cooper 2006). Much work remains to be done on this question of the origins of immunity, including by developing cross-species comparative immunology.

What has been said here about the expansion of the scope of immunity can also be framed in terms of the long-standing debate in the philosophy of biology about functions (Reference WrightWright 1973; Reference CumminsCummins 1975). Bodily systems generally have been viewed as obvious instances of a valid functional ascription: the function of the digestive system is to digest, the function of the respiratory system is to breathe, and so on. According to the traditional view of immunity, the function of the immune system is to defend the organism. Following this tradition, some philosophers have suggested (Reference Matthen and LevyMatthen and Levy 1984; Reference MelanderMelander 1993) that the function of the immune system, in the etiological sense (that is, what it has been selected for) (Reference WrightWright 1973), is organism defense. Yet saying what the immune system has been selected for proves, in fact, extremely difficult. Given the various activities of the immune system and the diversity of selective pressures it has undergone, it would be inadequate, or at least too restricted, to say that the immune system has been selected for its capacity to defend the organism against pathogens. It is not possible to single out one of these aspects and say that this is “the function” (or even “the main function”) of the immune system. It seems likely that the systemic approach to functions (Reference CumminsCummins 1975) is certainly better suited for immunology, but a detailed analysis of the promises and limitations of a systemic approach to immune functions remains to be done.

2.5 Is It Still Possible to Offer a Precise and Simple Definition of Immunity?

The extension of the scope of immunity well beyond defense affects dramatically the meaning of the term immunity and raises a thorny but central problem: given the diversity of phenomena in which the immune system plays a crucial role, is there still a unity of the concept of immunity, or is it just the loose and artificial putting together of a horde of processes under a single term? In other words, is there ultimately such a thing as immunity that unifies all of these processes under a single concept? I see this question as one of the most fascinating that current and future immunology must face. Defining what counts as an immune process and delineating the field of immunology has indeed become extremely challenging nowadays. Focusing on defense against pathogens would be too narrow. On the other hand, extending the definition of immunity so far as the overall physiological regulation of the body (as sometimes suggested by recent studies on the role of the immune system in metabolism, tissue repair, homeostasis, development, and so on) would be so broad that it might cease to be scientifically fruitful, as almost everything in biology could be said to be immunological, at least to some degree. One possibility would be to say that any component involved in a series of activities that includes defense against pathogens is part of immunity (in this conception, immunity would be centered on, but not limited to defense), but this option would still leave us with a broad conception of immunity. Uncertainties of this kind have led to a situation in which, perhaps unsurprisingly, current immunologists do not offer a single and consensual response to the question “What is immunity?”

I have tried in the past to put forward a definition of immunity according to which immunological processes correspond to all the processes of biochemical recognition of a target, followed by the elimination or the regulation of the elimination of this target (Reference PradeuPradeu 2012). This definition is not without difficulties (particularly concerning the level(s) at which it is supposed to apply), but I think it does capture the diversity of phenomena currently studied by immunologists, while remaining sufficiently specific so as not to include all classically understood physiological processes occurring in the organism. It also has the advantage of reflecting the diversity of immune systems in nature, from prokaryotes to vertebrates. More research is needed, though, to determine whether a definition of this kind could satisfy the majority of immunologists.

A related but broader and more imprecise characterization of immunity is to say that immunity is one of the main devices insuring the cohesion of the organism and the delineation of its boundaries. We will explore and assess this view in the next section, which is devoted to immunology’s contribution to the definition of biological individuality.

In summary, this section has shown that immune defense is essential in every living thing, but immunity cannot be reduced to defense.

3.1 From Early Reflections about Immunological Individuality to the Concepts of “Self” and “Nonself”

The key contribution of immunology to the reflection on biological individuality and identity ever since the end of the nineteenth century has been emphasized by historians and philosophers of this field over the last three decades (Reference Löwy and TauberLöwy 1991; Reference MoulinMoulin 1991; Reference TauberTauber 1994; Reference PradeuPradeu 2012; Reference Anderson and MackayAnderson and Mackay 2014). Here my goal is not to go into the details of that history, but rather to show how these early thoughts have been revisited in recent immunology.

The idea that immunological reactions had something to do with the questions of bodily individuality and identity was expressed as early as the end of the nineteenth century by many scientists, including, for example, Charles Richet (Reference RichetRichet 1894; Reference Löwy and TauberLöwy 1991). The many attempts to transplant body parts (especially the skin, which happens to be, in fact, an extremely difficult transplantation) in the wake of the First World War, however, constituted an important turning point, as it led many biologists and medical doctors to raise specifically the question of the biological determinants of the uniqueness of each individual and its capacity to recognize these unique determinants and to potentially detect and respond to elements that differ from them (Reference LoebLoeb 1937; Reference MedawarMedawar 1957).

Starting from the 1940s, Frank Macfarlane Burnet (1899–1985) (Reference BurnetBurnet 1940; Reference Burnet and FennerBurnet and Fenner 1949) framed the concepts of immunological “self” and “notself” (later called “nonself”) (Reference Löwy and TauberLöwy 1991; Reference MoulinMoulin 1991; Reference TauberTauber 1991; Reference Anderson and MackayAnderson and Mackay 2014). In its most basic form, the self–nonself framework says that the elements originating from an organism (the “self”) do not trigger an immune response, while elements foreign to this organism (the “nonself”) trigger an immune response. Such a framework can account for the rejection by the body of both infectious agents and grafts. The self–nonself vocabulary played an important role in establishing the study of infectious diseases as well as research on transplantation as subdomains of the science of immunology.

Burnet saw as a major challenge the question of how an organism can learn to preserve the constituents of the “self.” Partly inspired by Ray Owen’s work on chimerism (Reference OwenOwen 1945), Burnet postulated that, if foreign material was implanted early in the embryo, no antibodies would develop against that particular foreign material (Reference Burnet and FennerBurnet and Fenner 1949). This was later confirmed by experiments made by Peter Medawar’s group, showing that a tissue implanted early in the mouse embryo could subsequently be tolerated (Reference Billingham, Brent and MedawarBillingham et al. 1953). For Burnet, therefore, the self is acquired, not innate: the organism acquires at an early ontogenetic stage the capacity to recognize its own constituents and to avoid their destruction (Reference Burnet and FennerBurnet and Fenner 1949; Reference BurnetBurnet 1969). But Burnet argues that, in nature, contrary to what happens in these experimental settings, the immunological self reflects the genetically endogenous components of the organism because the repertoire of immune receptors is constituted on the basis of these endogenous elements present in the body (Reference BurnetBurnet 1962). Burnet considers several obvious challenges to the self–nonself framework, including autoimmune diseases and foeto-maternal tolerance as well as other forms of immunological tolerance (that is, the absence of destruction of a foreign entity by the immune system). But he treats them as exceptions to the general rule and considers that these exceptions must be explained via specific mechanisms (pathological mechanisms in the case of autoimmune diseases, and particular provisory mechanisms in the case of foeto-maternal tolerance) (Reference BurnetBurnet 1969). All these reflections constituted the foundations of a fruitful theoretical and conceptual framework about the self and nonself, which was developed by Burnet over more than three decades, and which combined in an innovative way molecular, cellular, ecological, and medical considerations (Reference BurnetBurnet 1940, Reference Burnet1969, pp. 309–310). Burnet shared the 1960 Nobel Prize in Physiology/Medicine with Medawar for what was essentially a contribution of a conceptual and hypothetical nature, as acknowledged by Burnet himself (Reference BurnetBurnet 1960, p. 700).

From a theoretical viewpoint, what Burnet sees as his main contribution to immunology is not primarily the self–nonself theory but rather the “clonal selection theory.” The clonal selection theory goes against instructionist approaches to antibody formation (especially that of Linus Pauling) by stating that, when an antigen penetrates into the organism, immune cells bearing receptors specific for this antigen undergo selection and are subsequently responsible for the elimination of that antigen (Reference BurnetBurnet 1959, p. 54). Burnet therefore proposes the adoption of a Darwinian framework at the cell level within the multicellular organism (Reference BurnetBurnet 1959, p. 64) – an idea that had been suggested before him but that Burnet framed in a much more precise way (Reference SchaffnerSchaffner 1992; Reference SilversteinSilverstein 2002).

Nonetheless, the clonal selection theory and the self–nonself theory are intimately connected, so much so that Burnet generally argues for them in parallel (e.g., (Reference BurnetBurnet 1959, Reference Burnet1969)). The phenomena that the clonal selection theory seeks to explain are immune recognition of the antigen, immune tolerance, and the acquisition of “self-knowledge” by the organism. To account for these phenomena, Burnet proposes the existence of two selective processes: one occurs in adult life, when an antigen enters into the body, as we just saw; but another selective process occurs long before, in early life, and this other process is the elimination of immune cells that recognize “self” components (Reference BurnetBurnet 1959). This explains why, in 1969, Burnet writes that the clonal selection theory provides “the simplest possible interpretation of how the body’s own constituents are shielded from immunological attack” (Reference BurnetBurnet 1969, p. 12).

From the second half of the twentieth century to the present day, the self–nonself framework has been adopted by a large majority of immunologists and enriched by a host of experimental, conceptual, and theoretical contributions (e.g., Reference Bretscher and CohnBretscher and Cohn 1970; Reference von Boehmer and Kisielowvon Boehmer and Kisielow 1990; Reference JanewayJaneway 1992; Reference Langman and CohnLangman and Cohn 2000). Today, the self–nonself remains the dominant, if often implicit, framework in which immunologists conceive how the immune system works (e.g., Reference Stefanová, Dorfman and GermainStefanová et al. 2002; Reference Goodnow, Sprent, de St Groth and VinuesaGoodnow et al. 2005; Reference Jiang and ChessJiang and Chess 2009; Reference Fulton, Hamilton and XingFulton et al. 2015). This is particularly illustrated by the fact that when a novel immune system is identified, as recently happened with the CRISPR-Cas systems in archaea and bacteria, scientists spontaneously use the self–nonself vocabulary to account for its functioning (Reference Nuñez, Harrington and KranzuschNuñez et al. 2015) (this comes in addition to the idea of CRISPR-Cas as a system of defense, as discussed in the previous section). Together with the persistent use of the self–nonself vocabulary in several other domains (including, for instance, studies on autoimmune diseases and transplantation), this confirms the long-standing influence of this framework in immunology over the last six decades.

3.2 Autoimmunity, Tolerance, and Symbiotic Interactions with Microbes

Despite its undeniable success as an encompassing conceptual framework for immunology, the self–nonself theory faces many difficulties. First, far from being always pathological, autoimmunity has been proved to be a necessary component of everyday immunity. A degree of autoreactivity (i.e., reaction to “self”) characterizes the lymphocytes generated and selected in primary lymphoid organs as well as naïve lymphocytes circulating in the periphery (Reference Tanchot, Lemonnier and PérarnauTanchot et al. 1997; Reference Anderton and WraithAnderton and Wraith 2002; Reference Hogquist and JamesonHogquist and Jameson 2014). Effector T cells are selected only if they react weakly to self elements (and not if they do not react at all). Moreover, strong autoreactivity in the thymus can lead to the selection and differentiation of lineages specific to self elements, including regulatory T cells (cells that dampen the activation of the immune system and play a key role in the prevention of autoimmune diseases) (Reference Wing and SakaguchiWing and Sakaguchi 2010). In addition, many effector immune responses that occur routinely at the periphery during the lifetime of an organism target endogenous (“self”) elements, as illustrated by the phagocytosis of dead cells, the clearance of cellular debris, many immune-mediated repair mechanisms, and the downregulating action of regulatory T cells, among many other phenomena. In other words, the claim that the immune system does not respond to self components is not true. There exists in fact a continuum from autoreactivity (interactions between immune receptors and endogenous motifs) to autoimmunity (the triggering of an effector response targeting endogenous motifs) and to autoimmune diseases (only the latter situation is pathological; it consists in the destruction of endogenous components, in a sustained manner and on a large scale – a given organ or even the whole organism in the case of systemic autoimmune diseases such as lupus) (Reference PradeuPradeu 2012).

Second, many genetically foreign entities are not eliminated by the immune system and are instead actively tolerated via regulatory immune responses. This includes examples such as foeto-maternal tolerance and various forms of chimerism, but also, and most crucially, immunological tolerance to a large number of bacteria, archaea, viruses, and fungi at all of the body’s interfaces, including the gut, skin, lungs, sexual organs, and so on (Reference Hooper and GordonHooper and Gordon 2001; Reference Chu and MazmanianChu and Mazmanian 2013; Reference VirginVirgin 2014; Reference Chen, Fischbach and BelkaidChen et al. 2018). These resident entities, which are found in almost all living things in nature, are often referred to as the “microbiota.” Contrary to what was thought for many years, these microbes are not “invisible” to the host immune system. The immune system interacts and develops an active dialogue with them, which leads to the triggering of a complex balance of effector and immunoregulatory mechanisms. In many cases, the host immune system facilitates the establishment and stability of certain components of the microbiota (Reference Round and MazmanianRound and Mazmanian 2009; Reference Donaldson, Ladinsky and YuDonaldson et al. 2018). Importantly, microbial molecular patterns that were conceived for a long time as pathogenic signatures can also mediate tolerogenic immune responses (Reference Sansonetti and MedzhitovSansonetti and Medzhitov 2009). All this confirms the centrality of the phenomenon of immunological tolerance, especially to the microbiota, in today’s immunology (Reference Pradeu and CarosellaPradeu and Carosella 2006a; Reference PradeuPradeu 2012).

Immunological interactions between host and microbes enable, in general, a peaceful coexistence between these two partners. It is estimated that a human host, for example, is made up of as many bacterial cells as its genetically self cells (Reference Sender, Fuchs and MiloSender et al. 2016). Yet the most central point is not so much the number of these resident microbes as what they do in the organism. The involvement of bacteria in digestion has been known for decades, but recent research has shown that resident microbes play a major and sometimes even indispensable role in host activities as diverse as development, metabolism, defense, tissue repair (Reference McFall-NgaiMcFall-Ngai 2002; Reference Xu and GordonXu and Gordon 2003; Reference McFall-Ngai, Hadfield and BoschMcFall-Ngai et al. 2013), as well as many other processes, including behavior (Reference Sharon, Sampson, Geschwind and MazmanianSharon et al. 2016; Reference Vuong, Yano, Fung and HsiaoVuong et al. 2017; Reference Schretter, Vielmetter and BartosSchretter et al. 2018a). The fitness benefit for microbes consists generally in particularly favorable niches, where they find nutrients and protection from competitors, among other things (Reference Donaldson, Lee and MazmanianDonaldson et al. 2016). Microbes can also manipulate their host in many different ways (Reference Sansonetti and Di SantoSansonetti and Di Santo 2007). Finally, it is crucial to understand that the interaction between host and resident microbes is the product of a complex equilibrium, in which the nature of the ecological relationship can change through time depending on the circumstances and switch from mutualism to commensalism to parasitism (microbes that switch from the status of symbionts to pathogens have sometimes been called “pathobionts” (Reference Chow, Tang and MazmanianChow et al. 2011)).

Recent work on immunological tolerance and the intimate dialogue between host and microbes across the living world invalidates the claim that the immune system eliminates foreign (nonself) entities. In the last two decades, symbiosis in general and symbiotic interactions with microbes more specifically have been recognized as ubiquitous and essential phenomena in nature. The specific contribution of immunology to this literature is to ask how symbiotic entities can be tolerated by the immune system and how they interact with this system in several central physiological processes (see Box 3.1).

The upshot is that the self–nonself theory is inadequate or at least incomplete, because many self components trigger immune responses and many nonself components are actively tolerated by the immune system. Therefore, today’s immunology calls for novel and richer theoretical frameworks (Reference JanewayJaneway 1989; Reference Grossman and PaulGrossman and Paul 1992; Reference MatzingerMatzinger 2002; Reference Pradeu, Jaeger and VivierPradeu et al. 2013), as well as renewed reflections about immunological individuality. The next section shows why, despite the critique of the self–nonself theory presented here, the claim that the immune system is pivotal for the definition of biological individuality remains entirely valid.

3.3 Immunology’s Contribution to the Definition of Biological Individuality

At the most general level, the issue of biological individuality consists in asking what makes up a countable, relatively well-delineated, and cohesive entity in the living world (Reference Sober and TauberSober 1991; Reference Hull, Keller and LloydHull 1992). (Being countable and well-delineated concerns what can be called external unity, whereas cohesion has to do with internal unity.) Yet the meaning of countability, delineation, and cohesion remains unclear and is therefore a matter of debate among philosophers of biology and biologists. Accounts of these three dimensions have generally been based either on intuition or on evolutionary theory (Reference Hull, Keller and LloydHull 1992; Reference Godfrey-SmithGodfrey-Smith 2009), leaving aside, in most cases, other biological fields, including physiological ones. In all these accounts the idea of “cohesion” seems particularly diverse and equivocal: a range of concepts have been suggested to elucidate this idea, including “functional integration” (the fact that parts are interconnected and interdependent) (Reference Sober and TauberSober 1991), “near-complete decomposability” (the fact that interactions between parts of the individual are stronger than interactions between parts of the individual and the environment) (Reference Simon and HerbertSimon 1969; Reference WimsattWimsatt 1972), and “cooperation and absence of conflict” (Reference Queller and StrassmannQueller and Strassmann 2009), but these concepts only partly overlap, and they are not always easy to define and to apply.

There is nowadays a quasi-consensus that biological individuality is question-dependent and practice-dependent, can be realized at different levels, comes in degrees, and should not be based on intuitions or on an anthropocentric approach (Reference PradeuPradeu 2016a; Reference Lidgard and NyhartLidgard and Nyhart 2017). I agree with this consensus. The specific question raised here is in what sense and to what extent the domain of immunology contributes to addressing the problem of biological individuality, essentially from a physiological point of view. (Section 5 discusses how to combine this approach with other approaches to biological individuality, including evolutionary ones.)

The main claim of this section is that immunology makes an important contribution to the definition of biological individuality insofar as it sheds light on all three dimensions discussed above, namely countability, delineation, and cohesion. The three main activities of the immune system participating in the individuation of biological entities can be called “filtering over entry,” “filtering over presence,” and “promotion of cooperation” (by “filter” I mean allowing or, on the contrary, restraining the entry or presence of something, as explained below). As Figure 3.1 indicates, these activities map onto countability, delineation, and cohesion.

Figure 3.1

The three main activities by which the immune system participates in the individuation of biological entities and how they map onto the traditional conception of a biological individual. Filtering over entry sheds light on the idea of the individual as a countable and relatively well-delineated entity, while filtering over presence and promotion of cooperation shed light on the idea of the individual as a cohesive entity.

“Filtering over entry” refers to the fact that the immune system constantly patrols the interfaces of the organism with the environment (skin, gut, and so on) and determines which exogenous elements can enter the organism and which can’t. It thus plays a decisive role in the delineation of the organism’s boundaries and the possibility of counting it as one single entity.

But the immune system does much more than control entries into the organism at interfaces. In a process that can be called “filtering over presence,” the immune system constantly monitors the motifs expressed by the cells present in all tissues and body compartments as well as their intracellular content and determines which elements are tolerated, and therefore can remain part of that living thing, and which elements are rejected, and therefore cannot remain part of that living thing. But what exactly does the immune system detect in this process of internal filtering? Although it has long been said that the immune system controls the identity of the elements with which it interacts (that is, their conformity with the self), my own view is that the immune system eliminates elements that change too abruptly, while tolerating elements that change slowly (Reference Pradeu, Jaeger and VivierPradeu et al. 2013). Regardless of the criterion one adopts, though, it remains that the immune system constitutes such a filter over internal elements in addition to filtering the entry of external elements at bodily interfaces.

Lastly, the immune system plays an important role in the promotion of cooperation between the components of the organism. It does so in two different ways. First, the immune system can ensure long-distance communication between remote components of the organism. In plants this is done through the vasculature and thanks to metabolites (Reference Shah and ZeierShah and Zeier 2013). In metazoans this is made possible by different processes, most prominently the unique mobility of immune cells. For example, immune cells can inform distant organs about the presence of a pathogen in the organism and also contribute to tissue remodeling in remote sites (Reference Eom and ParichyEom and Parichy 2017). As we will see in Section 5, other systems like the endocrine and the nervous systems are also capable of long-distance communication in metazoans, but the immune system is unique in its capacity to send cells to every compartment of the organism. Second, the immune system can eliminate noncooperative elements (“cheaters”), for instance, cancer cells (see next section) (Reference MichodMichod 1999; Reference FrankFrank 2007), via the detection of abnormal molecular patterns, cell stress, aberrant cellular proliferation, and/or damage caused to the organism (Reference MurailleMuraille 2013).

These last two activities (filtering over presence and promotion of cooperation) contribute to the cohesion of the biological individual (Figure 3.1). They strengthen functional integration (interconnection and interdependence), internal interactions (and therefore near-complete decomposability), as well as cooperation and absence of conflict between components.

Two important additional remarks are in order. First, the immune system is truly systemic, which means that, contrary to many bodily systems (e.g., digestive or respiratory), the immune system exerts its influence throughout the body. Therefore, filtering over entry, filtering over presence, and promotion of cooperation occur continuously and everywhere in the organism. (Many organs, either located at the interface with the environment or more internal, have been called “immunoprivileged” – for instance, the central nervous system and the eye, among many others. Yet recent research has shown that such compartments are not without immune influences (Reference Mellor and MunnMellor and Munn 2008; Reference Louveau, Harris and KipnisLouveau et al. 2015a). They are instead places where immunological processes are regulated differently than in the rest of the organism.)

Second, one crucial characteristic of the immunological approach to biological individuality is its broad range of application. It applies, in fact, to the whole living world, since immune systems are found in virtually all living things, including prokaryotes, plants, invertebrates, and vertebrates (see Section 2).

Thus, the immune system plays a central role in the delineation of the boundaries of a living thing and the determination of the cohesion between its constituents (Reference PradeuPradeu 2012). But is this account really different from the self–nonself framework examined above? It is actually essential to understand how the two accounts differ. For Burnet, the self–nonself framework is scientifically testable and useful if and only if self and nonself are defined in terms of origins: the self is what originates from the organism once it has acquired the capacity to recognize its own constituents, while the nonself is everything that does not originate from the organism. In stark contrast, the discrimination proposed above between what is part of the living thing and what isn’t is not based on a question of origin, since in this view many genetically foreign entities can be accepted by the immune system while many endogenous entities are routinely destroyed. For example, in the account developed here, microbiota components that are immunologically tolerated belong to the organism, while they are considered nonself and therefore not part of the organism in the self–nonself theory. In other words, I propose that the immune system contributes to the continuously re-delineated distinction between the “inside” and the “outside” but this distinction is not to be confused with the opposition between the “endogenous” (what comes from the inside) and the “exogenous” (what comes from the outside). The resulting living thing does not coincide with the traditional self and cannot be accounted for by Burnet’s self–nonself theory.

A related idea is that the process of dual filtering presented here is dynamic and never-ending. There is, therefore, a constant re-delineation, through the action of the immune system, of the constituents and boundaries of a living thing. This sheds a crucial light on the diachronic identity of biological individuals (Reference WigginsWiggins 2016). An entity that is part of a living thing at a given moment (for example, an immunologically tolerated virus) can cease to be part of that living thing later in time (for example, if this virus is eventually eliminated by the immune system). The resulting individuality is relative and changes continuously, but the criterion used to establish what is part and what is not part of a living thing remains constant and offers a precise delineation.

3.4 The Role of the Immune System in Turning a Set of Heterogeneous Constituents into an Integrated Individual

Immunology helps us better understand what makes a living thing a highly integrated individual despite the diversity of its constituents. (Like many other aspects of biological individuality, integration – which we defined as one way of conceiving cohesion – is a matter of degree.) According to the immunological account proposed here, every living thing is a chimera, a heterogeneous and mixed entity composed of genetically diverse components (Reference PradeuPradeu 2010; Reference DupréDupré 2010). On the one hand, it is a composite entity, comprising biotic elements that originate both from the organism and from outside the organism (bacteria, viruses, fungi, and so on). On the other hand, it is a very special composite entity, exhibiting a high degree of integration, with well-delineated boundaries, tight interactions, and strong cooperation between its components. Because of its three key activities of filtering over entry, filtering over presence, and promotion of cooperation, the immune system is essential in determining the constituents and boundaries of the living thing and therefore in turning a set of heterogeneous components into an integrated individual. In other words, the immune system exerts a major “e pluribus unum” activity: it constantly turns a plurality of elements that are diverse and of various origins into a cohesive unit. From this point of view, the immune system, along with other (and closely connected) “policing” mechanisms (such as apoptosis) and systems pertaining to adhesion and intercellular communication, participates in the “glue” of life, the sticking together of diverse elements that eventually constitute a physiological unit. (For a similar claim centered on the specific example of sponges, see (Reference MüllerMüller 2003).)

This reasoning allows us to propose an immunological definition of the organism, understood as a physiological individual (i.e., a cohesive whole, functioning collectively as a regulated unit that persists through time). According to this definition, an organism is a continuously changing, functionally integrated whole made up of heterogeneous constituents (including many microbes) that are locally interconnected by strong biochemical interactions and controlled at a systemic level by immunological interactions (Reference PradeuPradeu 2010). Everything that is actively interacting locally and tolerated by the immune system is part of the physiological individual.

This means that immunological processes can help us identify and delineate physiological individuals not via intuition and common sense (as has often been a concern with physiological definitions) but on the basis of a clearly formulated and scientifically grounded criterion (following the argument of (Reference Hull, Keller and LloydHull 1992)). The boundaries of the immunologically delineated living thing may be a matter of degree and vary depending on the context, but the criterion itself is precise and clear. For example, there are uncertainties and debates over what counts as a biological individual in the case of a colonial entity such as the ascidian Botryllus schlosseri (Figure 3.2): each cell, each zoid, the whole colony, or perhaps all of them together (Reference BussBuss 1999)? If we adopt the immunological perspective suggested here, then the whole colony should be recognized as the physiological individual because it is at the level of the colony that immunological processes occur such as histocompatibility-based fusion/rejection responses when two colonies meet (Reference De Tomaso, Nyholm and PalmeriDe Tomaso et al. 2005). Similarly, there are many discussions about whether or not the microbiota is part of the individual it inhabits (e.g., (Reference Gilbert, Sapp and TauberGilbert et al. 2012)). Our immunological account tells us that all (and only) the microbes that are immunologically tolerated are part of the physiological individual.

Figure 3.2

Rejection between two colonies of Botryllus schlosseri. When two colonies of Botryllus schlosseri meet, they can reject (panel A) or fuse (not shown). This occurs at the colony level. The brown zones show the starting point of rejection. Panel B shows rejection at the more precise level of ampullae.

(Photographs courtesy of Tony De Tomaso, UCSB)

Crucially, organismality here is a product, not a given. Indeed, my claim is not that the components of an already identified organism are tolerated by its immune system. Instead, I propose that it is the identification of a local concentration of biochemical and immunological processes taken together that tells us how to pick out organisms (understood as physiological individuals) in nature on the basis of the capacity of the immune system to determine what the constituents and boundaries of a living thing are. We start with an unindividuated living mass (Botryllus schlosseri, for example), but the identification of immunological processes allows us to single out and delineate quite precisely a physiological individual.

Biological individuation, as we saw, can be realized at different levels. An interesting aspect of immunological individuation is that it also can occur at different levels. Multicellular organisms exhibit what can be called a multilevel immunity: key immunological processes occur at the level of each cell (for example, any cell of the organism infected by a virus will respond by triggering a diversity of protective mechanisms, including the production of interferons and other cytokines – a phenomenon often referred to as cell intrinsic immunity – which can alter neighboring cells about the presence of the virus) (Reference Goubau, Deddouche and Sousa CGoubau et al. 2013) and at the level of each tissue. Most of the time, one can distinguish degrees of immunological responses: in most multicellular organisms, for instance, cell and tissue immunological responses are strongly controlled and coordinated at the systemic level, so the systemic level seems to be the level at which the highest degree of immunological integration is realized. Interestingly, in some cases, the highest degree of immunological integration is realized at the level of a colony rather than intuitively defined individuals. For example, some data in a number of social insects such as termites and honey bees suggest that key immunological processes occur at the colony level, which has led to the concept of “social immunity” (Reference Cremer, Armitage and Schmid-HempelCremer et al. 2007; Reference Jones, Shipley and ArnoldJones et al. 2018) and has sometimes been used to support the superorganism hypothesis.

The conclusion of this discussion is that recent immunological research has seen extensive revisions of its core concepts (particularly “self,” “tolerance,” and “microbe”), which in turn have led to a significant reassessment of our traditional understanding of biological individuality insofar as a living thing can be seen as an immunologically unified chimera (Reference Gill, Pop and DeBoyGill et al. 2006; Reference EberlEberl 2010; Reference Bosch and McFall-NgaiBosch and McFall-Ngai 2011; Reference PradeuPradeu 2012). But do these changes have any practical consequences? The short answer is that they have many practical consequences, particularly from a therapeutic point of view. Let’s take two examples of this – autoimmune diseases and ecological approaches to the microbiome.

If the perspective presented here is correct, then autoimmunity is a physiological process, which plays indispensable roles in the organism. Autoimmune diseases must be perceived not as the result of the sudden appearance of an undesirable autoimmune reaction (in the tradition of Ehrlich’s “horror autotoxicus”) and elimination of immune cells responding to the self, but as the consequence of a perturbation in the (cell-mediated, tissue-mediated, or system-mediated) regulation of immunological processes that include, as a normal component, responses to endogenous elements (Reference Wing and SakaguchiWing and Sakaguchi 2010). This means that, contrary to what has been done over the last decades, the first question of researchers interested in understanding autoimmune diseases should perhaps be not so much “what triggers an immune response against the self?” (e.g., why do self-reactive effector T cells develop in this organism?) as “which aspect of the regulatory machinery that normally keeps autoimmune responses in check has been disturbed, and why?” (e.g., why do regulatory T cells no longer downregulate the activity of potentially harmful autoreactive T cells?). The two strategies differ. The first acts at the level of effector cells and consists in preventing the development of autoreactive cells. The second acts at the level of the cells that regulate the activity of effector cells; acknowledging the physiological nature of autoimmunity, it consists in preventing the switch from physiological autoimmunity to pathological autoimmunity. One can speculate that many factors could play a role in this disturbance of regulatory mechanisms (especially regulatory T cells), including excessive hygiene in industrialized societies (Reference BachBach 2002), modification of the microbiota, and disorganization of the extracellular matrix in local tissues.

The second example of a therapeutic consequence of the renewed conception of immunity and individuality in recent immunology concerns the microbiota. Recognizing that most living things harbor myriad microbes, most of which do not harm their hosts, a key clinical goal becomes to manage these microbial communities instead of trying to kill all microbes. The development of such ecological approaches in medicine is a difficult task because the microbiota is in fact made of several highly complex local ecosystems in which any perturbation is likely to have unpredictable consequences. That being said, recent success with faecal transplantation in people infected with Clostridium difficile (Reference van Nood, Vrieze and Nieuwdorpvan Nood et al. 2013), despite major potential limits in other contexts (Reference PamerPamer 2014), suggests that such approaches are of increasing interest to clinicians. Another approach in the same vein is to determine to what extent, in a context of antibiotic resistance, it will be possible to manipulate components of the microbiota to protect a host against pathogens (Reference PamerPamer 2016).

3.5 Combining Different Approaches to Biological Individuality

Immunology is clearly not alone in shedding light on biological individuality, an issue to which many biological fields can contribute (Reference ClarkeClarke 2011; Reference PradeuPradeu 2016a; Reference Lidgard and NyhartLidgard and Nyhart 2017). First, the contribution of immunology, as we saw, concerns primarily the biological individual understood from a physiological point of view, and moreover it is not the only field contributing to that question (developmental biology, neuroscience, and many others also contribute). Second, beyond physiological fields, other biological domains, most prominently evolutionary biology, can shed light on the problem of biological individuality. In the last four decades or so, especially after the founding work of David Hull, most of the debates about biological individuality among philosophers of biology and biologists have focused on evolutionary individuality. This includes discussions over units of selection, the replicator/interactor distinction (Reference HullHull 1980), Darwinian individuals (Reference Godfrey-SmithGodfrey-Smith 2009), the possibility of defining species as individuals (Reference HullHull 1978; Reference HaberHaber 2016), the question of how groups of entities can aggregate and form new individuals (Reference BussBuss 1987; Reference Maynard Smith and SzathmáryMaynard Smith and Szathmáry 1995; Reference MichodMichod 1999), as well as multilevel selection and the constitution of an organism from an evolutionary viewpoint (Reference OkashaOkasha 2006; Reference Queller and StrassmannQueller and Strassmann 2009). Other fields also have much to say about the concept of a biological individual, including, for instance, ecology (Reference HunemanHuneman 2014).

Recently there have been many calls in favor of pluralistic and practice-oriented approaches to biological individuality (Reference KovakaKovaka 2015). As useful as these calls have been in undermining the idea that accounts of biological individuality based solely on a single scientific field (typically evolution, but the same would apply to any other “monistic” approach) and on a purely theoretical viewpoint would be sufficient, it is now important to take a step further. The existence of a plurality of approaches to biological individuality, many of which are rooted in certain scientific practices, is not disputable. The major challenge at present is to determine whether it could be useful to combine different approaches to biological individuality and, if so, how (Reference PradeuPradeu 2016b; Reference Lidgard and NyhartLidgard and Nyhart 2017). Some entities in the living world display a high degree of physiological and/or metabolic individuality without displaying a high degree of evolutionary individuality, or the other way around (Reference Dupré and O’MalleyDupré and O’Malley 2009; Reference PradeuPradeu 2010). Other entities, in contrast, may express a high degree of individuality on both grounds. Perhaps determining which entities express a high degree of individuality along several criteria tells us something important about their roles in the living world. An equally important issue is to establish to what extent different criteria of biological individuality are compatible or mutually exclusive. Indeed, even if scientific practices of individuation vary from one scientific field to another, there often is a significant overlap between the questions and criteria used by different biologists when they talk about biological individuals (Reference Guay and PradeuGuay and Pradeu 2016). This constitutes a promising research program for philosophers of biology interested in making comparisons across several scientific fields.

In summary, the immune system plays a major role across species in determining the boundaries, constitution, and cohesion of the biological individual. Far from the original concepts of self and nonself, today’s immunology tells us that a living thing can be seen as an immunologically integrated chimera. Although certainly not unique, the contribution of immunology to the long-standing debate over biological individuality is important, so much so that philosophers and biologists interested in that debate cannot neglect this contribution. What immunology has to say about individuality has long-reaching consequences for our understanding of what a living thing is, including what we are as humans, and it also impacts health issues of central importance, from autoimmune and inflammatory diseases to antibiotic resistance and transplantation.

4.1 How the Immune System Restrains Cancer: The Complex History of the Idea of Immunosurveillance

It is obviously difficult to make broad generalizations when discussing cancer. Most of the time, when we talk about cancer, we refer to a set of significantly heterogeneous diseases characterized by uncontrolled cell multiplication and the cells’ potential to invade other parts of the organism. The heterogeneity of cancer is a well-established point (Reference Melo, Vermeulen, Fessler and MedemaMelo et al. 2013; Reference BertolasoBertolaso 2016; Reference PlutynskiPlutynski 2018). First, cancers found in humans are quite diverse. Solid tumors (e.g., a carcinoma, a cancer that develops from epithelial cells, which constitutes the most frequent form of cancer) differ from liquid tumors (e.g., leukemia, a cancer that develops from bone marrow–derived cells). Cancers also differ from organ to organ: for example, a breast cancer can be quite unlike a skin cancer (this is called intertumor heterogeneity) (Reference Melo, Vermeulen, Fessler and MedemaMelo et al. 2013). Cancers affecting a given organ, such as the breast for example, can have different characteristics (Reference Zardavas, Irrthum, Swanton and PiccartZardavas et al. 2015). Moreover, a cancerous tumor can exhibit a high level of internal heterogeneity (“intratumoral heterogeneity”) (Reference Fisher, Pusztai and SwantonFisher et al. 2013). Last but not least, some tumors are benign, as they do not invade other body parts. Second, beyond humans, cancers exist in a great number of multicellular organisms, which further increases the diversity of cancer types and characteristics. If cancer is defined as a breakdown of multicellular cooperation that manifests itself by uncontrolled proliferation, inappropriate cell survival, resource monopolization, deregulated differentiation, and degradation of the environment, then it is found in many different groups, including starfish, hydra, insects, and plants (Reference Aktipis, Boddy and JansenAktipis et al. 2015).

Despite the diversity and heterogeneity of cancers, the immune system has been shown to be implicated in cancer progression in a large range of cancer types in various vertebrates (and also, if perhaps more speculatively given the limited number of studies, in invertebrates (Reference Pastor-Pareja, Wu and XuPastor-Pareja et al. 2008; Reference RobertRobert 2010)). Because of the publicity around cancer immunotherapies, most people are now aware that the immune system plays a role in cancer. Yet much remains to be done to understand the detailed mechanisms underlying this process. Study of the interactions between cancer and the immune system has undergone major transformations in the last two decades. To understand why the immune system can participate in the rupture of cohesion that characterizes cancer, it is essential to understand the nature of these recent transformations.

The history of the study of how the immune system influences cancer progression is itself illuminating. In the 1890s William Coley (Reference ColeyColey 1893) took advantage of the observation that spontaneous tumor regression could follow infection with a pathogen to develop a killed bacterial vaccine for cancer, a phenomenon in which immune components were thought to play a role (Reference Cann, Netten and NettenCann et al. 2003). At the beginning of the twentieth century, Paul Ehrlich suggested that the immune system could recognize and eliminate malignant cells (Reference EhrlichEhrlich 1909). In the mid-1950s, Lewis Thomas (at a symposium held in 1957, and published two years later (Reference Thomas and LawrenceThomas 1959)) and Macfarlane Burnet (Reference BurnetBurnet 1957) argued that cellular immunity was, in the words of Thomas, “designed as a useful and effective mechanism for the early sensing and early elimination of neoplastic cells” (Reference ThomasThomas 1982, p. 330). Thomas was convinced that humans produce tumors all the time but keep them under control, thanks to the action of the immune system. Burnet later expanded this idea and coined the term immunological surveillance (sometimes called immunosurveillance) (Reference BurnetBurnet 1970). According to immunological surveillance, the immune system is capable of detecting and eliminating the “altered self” (Reference HoughtonHoughton 1994), that is, “new antigens” (Reference BurnetBurnet 1970, p. 7) (antigens that are different from those of the body, also called “neoantigens” (Reference Schumacher and SchreiberSchumacher and Schreiber 2015)). In the 1970s, the idea of immunological surveillance started to decline because several experiments suggested that immunodeficient mice did not have a higher susceptibility to spontaneous or chemically induced tumors (Reference StutmanStutman 1974). As a result it was almost entirely abandoned for several years. A clear indication of this is the fact that the highly influential review on the “hallmarks of cancer” by Hanahan and Weinberg published in 2000 (Reference Hanahan and WeinbergHanahan and Weinberg 2000) ignores the role of the immune system in cancer (this was corrected in (Reference Hanahan and WeinbergHanahan and Weinberg 2011)).

At the beginning of the 2000s, a series of experiments showed the impact of the immune system on cancer development (Reference Shankaran, Ikeda and BruceShankaran et al. 2001; Reference Dunn, Bruce and IkedaDunn et al. 2002). The supposedly immunodeficient mice used in experiments from the 1970s onward to invalidate the idea of immunosurveillance in fact had an immune system (they had NK cells, γδ T cells, and even some αβ T cells) (Reference Dunn, Bruce and IkedaDunn et al. 2002). During this period, the involvement of both innate and adaptive immune components in cancer control was demonstrated (immunochemical or functional ablations of NKT, γδ T cells, NK cells, αβ T cells, IFN-γ, and interleukin 12 all lead to increased susceptibility to cancer).

4.2 The Dual Action of the Immune System in Both Restraining and Promoting Cancer: Immunoediting and Beyond

Although much emphasis has been put on the capacity of the immune system to restrain cancer, the immune system can also, perhaps paradoxically, promote cancer (Reference de Visser, Eichten and Coussensde Visser et al. 2006). Here again, both the innate and adaptive components of the immune system can participate in such cancer-promoting processes. One important step in the realization that the immune system can favor cancer development was the switch from the concept of immunosurveillance to that of immunoediting (Reference Dunn, Bruce and IkedaDunn et al. 2002). Several researchers working on immunosurveillance noted that the action of the immune system could lead to the selection of more resistant tumor cells. Highly immunogenic tumor cells are eliminated by the immune system, but this process leaves behind tumor variants of reduced immunogenicity (or that have acquired other mechanisms to evade or suppress the immune response) and have a higher fitness in the immunocompetent host (a process similar to the selection of more resistant pathogens). Therefore, Robert Schreiber and colleagues proposed to use the term immunoediting instead of the traditional notion of immunosurveillance, reflecting the fact that the immune system not only monitors tumors but also shapes them, with both beneficial and detrimental consequences for the host (Reference Dunn, Bruce and IkedaDunn et al. 2002; Reference Schreiber, Old and SmythSchreiber et al. 2011). Immunoediting is a more encompassing and more accurate concept, especially because it emphasizes the diachronic character of cancer development.

The concept of immunoediting is well-suited to describe the dual host-protecting and tumor-sculpting actions of the immune system. According to its proponents, immunoediting encompasses three different though largely overlapping processes, referred to as the “3 e’s” (see Figure 4.1): “elimination” (which corresponds to the classic idea of immunological surveillance, that is, the destruction of tumor cells by the immune system), “equilibrium” (the immune system iteratively selects and/or promotes the generation of tumor cell variants with increasing capacities to survive immune destruction), and “escape” (the immunologically sculpted tumor expands beyond control in the host) (Reference Dunn, Bruce and IkedaDunn et al. 2002). In 2007, a landmark study by Schreiber’s group confirmed the existence of the equilibrium phase (Reference Koebel, Vermi and SwannKoebel et al. 2007).

Figure 4.1

The three phases of immunoediting. According to the concept of immunoediting, three phases must be distinguished in the interactions between the immune system and the tumor: (a) elimination, which corresponds to the destruction of tumor cells by the immune system; (b) equilibrium, in which the immune system selects and/or promotes the generation of immunologically resistant tumor cell variants; and (c) escape, which corresponds to the expansion of the immunologically shaped tumor that is now beyond the control of the immune system.

(Figure drawn by Wiebke Bretting, after (Dunn et al. 2002)).

The processes by which the immune system can have a tumor-promoting effect go well beyond immunoediting and are actually quite diverse. In particular, tumor-associated macrophages (TAMs) can sometimes be tumor-suppressive, but in a majority of cases they favor tumor initiation, progression, and metastasis (Reference Mantovani, Bottazzi and ColottaMantovani et al. 1992; Reference Wynn, Chawla and PollardWynn et al. 2013). Indeed, macrophages can sustain the chronic inflammation that often plays a role in tumor initiation and promotion (Reference Mantovani, Allavena, Sica and BalkwillMantovani et al. 2008), skew adaptive immune responses, and facilitate cell growth, angiogenesis (Reference Murdoch, Muthana, Coffelt and LewisMurdoch et al. 2008), matrix deposition, tissue remodeling (Reference Mantovani, Biswas and GaldieroMantovani et al. 2013; Reference Afik, Zigmond and VugmanAfik et al. 2016), and metastasis (Reference Qian and PollardQian and Pollard 2010). The exact effects of macrophages located in or around the tumor also depend on the temporal sequence of events: tumor-preventing macrophages can switch to a tumor-promoting role depending on the cues they receive from the tumor microenvironment (Reference Wynn, Chawla and PollardWynn et al. 2013). So-called myeloid-derived suppressor cells (MDSCs) contribute to cancer and metastasis (Reference Kumar, Patel, Tcyganov and GabrilovichKumar et al. 2016), and tumor-associated neutrophils (Reference Fridlender, Sun and KimFridlender et al. 2009) as well as regulatory T cells (Reference Tanaka and SakaguchiTanaka and Sakaguchi 2017) also, in many circumstances, can promote cancer.

4.3 Immune–Cancer Interactions: Current Views and Clinical Applications

Today, the evidence showing that the immune system plays a central role in cancer development (either preventing or promoting cancer) is overwhelming (Reference Schreiber, Old and SmythSchreiber et al. 2011; Reference Chen and MellmanChen and Mellman 2017; Reference Ribas and WolchokRibas and Wolchok 2018). Many cellular and molecular immune components are involved in this process of restriction or promotion of cancer. Additionally, these interventions of the immune system can occur at different levels in or around the tumor (including genes, cells, and the tumor microenvironment) and at every step of its progression, from initiation to neoplastic progression to metastasis. For example, mouse models showed that tumor-associated macrophages promote angiogenesis and tissue remodeling, thereby favoring tumor growth. Clinical studies show that extensive tumor-associated macrophage infiltration positively correlates with cancer metastasis and poor clinical prognosis (Reference Afik, Zigmond and VugmanAfik et al. 2016)

Investigations about the role of the immune system in cancer progression have led to remarkable clinical applications. For example, several groups have shown how, in a diversity of cancers, infiltration by certain immune components had a better prognostic value than more traditional approaches (Reference Galon, Costes and Sanchez-CaboGalon et al. 2006). But most crucially, since the 2010s, the knowledge accumulated over decades about immune-mediated control of cancerous tumors has turned into specific clinical applications called “cancer immunotherapies,” which many have described, rightly or wrongly, as “revolutionary” (Reference KellyKelly 2018). After extremely encouraging results obtained in melanoma and a few other cancer types at the beginning of the 2010s (Reference Hodi, O’Day and McDermottHodi et al. 2010; Reference Wolchok, Kluger and CallahanWolchok et al. 2013), evidence in favor of the success of immunotherapies (increasingly, in fact, a combination of immunotherapies) in several cancers has accumulated (Reference Ribas and WolchokRibas and Wolchok 2018). In a number of situations, the results have been unprecedented and sometimes even spectacular, especially in cases of previously incurable cancers, raising much enthusiasm. Immunotherapies are diverse but recently immune checkpoint inhibitors have been particularly explored (Reference Leach, Krummel and AllisonLeach et al. 1996; Reference Ribas and WolchokRibas and Wolchok 2018).

The most significant recognition of the work done in this area is undoubtedly the 2018 Nobel Prize in Physiology/Medicine awarded to James P. Allison and Tasuku Honjo “for their discovery of cancer therapy by inhibition of negative immune regulation,” which is centered on the blockade of immune checkpoints. This has definitely convinced researchers working in all areas of cancer investigation and the lay public that it is indispensable to pay attention to the role of the immune system in cancer. It comes as no surprise that many newspapers have discussed these medical advances, if perhaps sometimes hyperbolically (e.g., (Reference VonderheideVonderheide 2018)).

Are immunotherapies really revolutionary, and what do they tell us about immune–cancer interactions? From a strictly medical point of view, this enthusiasm is justified, although we should keep in mind that some important limits exist. The first limit is the low percentage of responders: less than 15 percent on average, though it depends on tumor type and on the category of immunotherapy (Reference Haslam and PrasadHaslam and Prasad 2019). (Future research likely will significantly extend the proportion of responders.) A second limit is the existence of sometimes significant adverse effects (immunotherapies, in particular, increase the level of inflammation and autoimmune responses, which can lead to colitis, hepatitis, etc.) (Reference Postow, Sidlow and HellmannPostow et al. 2018). A third limit is the currently exorbitant cost of some treatments.

From a conceptual viewpoint, therapies based on immune checkpoint inhibition constitute indeed a radical change in perspective (Reference Lesokhin, Callahan, Postow and WolchokLesokhin et al. 2015; Reference Sanmamed and ChenSanmamed and Chen 2018). At least two important features of immune checkpoint therapies are worth emphasizing. First, the target of the treatment is the immune system, not the tumor itself (as was the intention with traditional treatments such as surgery, chemotherapy, and radiotherapy – although, in fact, some of them are now known to act at least in part via stimulation of the immune system (Reference Galluzzi, Senovilla, Zitvogel and KroemerGalluzzi et al. 2012)). Second, the objective is to break the state of immune tolerance that has been established between the tumor and the immune system in the local tissue (Reference Lesokhin, Callahan, Postow and WolchokLesokhin et al. 2015; Reference Ribas and WolchokRibas and Wolchok 2018) – partly as a consequence of the chronic expression of cancer antigens (Reference Pauken and WherryPauken and Wherry 2015). More precisely, the aim with immune checkpoint blockers is to downregulate inhibitory signals in tumor–immune interactions. This constitutes a move from enhancement of the immune system to “normalization” of the immune system: in immune checkpoint inhibitor-based immunotherapies, especially with anti-PD-L1, the aim is not, strictly speaking, to boost the immune system beyond its normal rate of activation but to restore a local context in which the immune system will be able to act as it normally does (Reference Sanmamed and ChenSanmamed and Chen 2018).

Together, basic studies about the role of the immune system in cancer and clinical studies in the domain of immunotherapies also have contributed to an important change in perspective about what cancer is and how it develops (Reference PrendergastPrendergast 2012). It is increasingly recognized that tumor-centric views of cancer (with genetic mutations seen as the main cause of cancer) are insufficient: to understand (and cure) cancer, it is essential to consider not only the tumor itself but also the tumor environment ((Reference Bissell and HinesBissell and Hines 2011; Reference Maman and WitzMaman and Witz 2018); for conceptually and philosophically-oriented analyses, see (Reference BertolasoBertolaso 2016; Reference LaplaneLaplane 2016; Reference PlutynskiPlutynski 2018)). The tumor environment includes the tissue context located at the vicinity of the tumor (sometimes called the tumor microenvironment), but also elements located quite remotely from the tumor in the organism (such as some immune-associated organs and the microbiota, which recently has been proven to influence cancer progression and therapies) (Reference Zitvogel, Ma and RaoultZitvogel et al. 2018; Reference Binnewies, Roberts and KerstenBinnewies et al. 2018; Reference Laplane, Duluc and LarmonierLaplane et al. 2018). Even authors who initially focused on intrinsic molecular aspects of cancer development have later emphasized the importance of the tumor microenvironment (Reference Hanahan and WeinbergHanahan and Weinberg 2011). Targeting the tumor microenvironment also offers enriched therapeutic strategies (e.g., (Reference JoyceJoyce 2005)). There is a growing consensus that the immune system plays a crucial role in the tumor microenvironment (Reference Bissell and RadiskyBissell and Radisky 2001; Reference Binnewies, Roberts and KerstenBinnewies et al. 2018; Reference Maman and WitzMaman and Witz 2018). In fact, given the centrality of immune components in the organization of, and control over, the local tissue, it seems reasonable to say that every cancer involves the immune system, which necessarily intervenes, at one point or another, in the shaping of the local context that enables the tumor to emerge, grow, and perhaps spread.

4.4 Role of the Immune System in the Breakdown of Biological Individuality That Characterizes Cancer

With all this discussion over the tumor-restricting and tumor-promoting roles of the immune system in mind, we can now return to the question with which we started. What exactly is the role of the immune system in the prevention of the breakdown of individuality that characterizes cancer, and how can the immune system be involved, conversely, in the decohesion of the biological individual?

The idea that cancer constitutes a breakdown of biological individuality is widespread in the scientific and philosophical literature. Biologist Leo Buss was instrumental in showing that biological individuality in multicellular organisms must be understood as an outcome of evolution, by which, on several occasions in life’s history, some cells aggregated and cooperated, and in which emerged some control mechanisms over cells that would proliferate at the expense of the whole organism (Reference BussBuss 1987). Buss takes cancer as an example of a decohesion of the biological individual, in which cancer cells are “re-individualized” in a way that becomes harmful to the multicellular organism. This idea has subsequently been explored by several biologists and philosophers of biology (Reference FrankFrank 2007; Reference GermainGermain 2012; Reference PlutynskiPlutynski 2018), often inspired by the study of clonal evolution at the cell level in cancer (Reference NowellNowell 1976; Reference Greaves and MaleyGreaves and Maley 2012). For example, Godfrey-Smith labels as “de-darwinization” the process by which a higher-level individual prevents proliferation of lower-level individuals (Reference Godfrey-SmithGodfrey-Smith 2009, pp. 100–103). From that point of view, cancer cells appear as a result of a “re-darwinization” at the cell level.

However, the mechanistic details by which the multicellular organism exerts control over cancer cells have remained vague. Michod (Reference MichodMichod 1999, p. 119) cites programmed cell death and the immune system as the two main “policing mechanisms” in the multicellular organism, but he does not give any detailed explanation about how they work. An important lesson of what has been said in this section is that immunological surveillance constitutes a convincing example of a mechanistically precise process of maintenance of cohesiveness in the organism (Reference PrendergastPrendergast 2012; Reference Pradeu, Bouchard and HunemanPradeu 2013). Thus, it offers an important contribution to this long-standing debate concerning de-darwinization in cancer. The details of how immune-mediated control works are well documented: in the elimination phase of immunoediting, myriad immune cells and molecules (macrophages, dendritic cells, NK cells, γδ T cells, CD4 and CD8 T cells, IFN-γ, among many others) contribute to the destruction of the tumor (Reference Dunn, Bruce and IkedaDunn et al. 2002). In addition, immune-mediated control contributes to coordinate other control instruments, such as apoptosis and angiogenesis.

This, however, strengthens rather than solves the paradox: if immune-mediated restriction is one of the main mechanisms ensuring the cohesion of the organism, we need an explanation for why in some circumstances the immune system favors tumor development (through the escape phase of immunoediting and/or through repair mechanisms that contribute to creating a favorable tissue environment for the tumor). To better understand this phenomenon, I propose here an extended view of immune-mediated cohesion and decohesion.

The traditional view about immune-mediated cohesion, as represented in classically defined immunological surveillance, is that the immune system can eliminate abnormal cells such as cancer cells (Figure 4.2).

Figure 4.2

The traditional view of immune-mediated cohesion, as proposed by the immunological surveillance hypothesis. According to this view, the immune system directly eliminates abnormal cells, such as cancer cells (in red) in the tumor.

(Figure drawn by Wiebke Bretting).

This view, however, is too narrow, because it neglects the diversity of activities in which the immune system is involved, which include not only defense but also development, tissue repair, clearance of debris, and maintenance of tissue homeostasis, among others (see Section 2). In cancer, many of these immunological activities are found. This leads to a much richer view of immune-mediated cohesion and decohesion in cancer (Figure 4.3). In this view, the immune system plays a major role in regulation of the organization of the local tissue, and, together, the immune system and the tissue realize different activities, including the elimination of abnormal cells, but also the containment of abnormal cells (in that case, cells are not destroyed, they are simply kept under control, which limits the damage they can do and/or their capacity to spread), the maintenance of chronic elements present in the local environment (most of the time, these chronic elements are normal self components of the organism, but chronically present tumor constituents can also lead to active maintenance of the tumor by the immune system, which progressively sees these elements as normal) (Reference Pradeu, Jaeger and VivierPradeu et al. 2013; Reference Pauken and WherryPauken and Wherry 2015), and the repair of the local tissue (in physiological conditions, this repair is a necessary process insuring the integrity of the tissue, but in the context of cancer repair mechanisms can favor cancer progression).

Figure 4.3

A richer view of immune-mediated cohesion and immune-mediated decohesion in cancer. In this view, the immune system controls tissue organization and, together, the immune system and the local tissue can exert a variety of cohesion-promoting activities, including the elimination of abnormal cells, but also the containment of abnormal cells, the maintenance of chronic elements, and tissue repair. All these activities (not just elimination), in pathological conditions, can promote decohesion of the organism.

(Figure drawn by Wiebke Bretting).

The crucial point here is that decohesion as seen in cancer can concern all these different activities, not just elimination: the immune system, which in most cases prevents cancer progression by elimination, containment, maintenance, and repair, can in some circumstances promote cancer progression because of deregulated elimination, containment, maintenance, and/or repair. Moreover, all these activities must be understood diachronically: they do not all intervene at the same time, and the immune system can switch from one effect to the other (for example, it can initiate the destruction of abnormal components and later contribute to their maintenance because they have become chronically expressed in the tissue).

Does the immune system dysfunction when it promotes cancer progression via a deficit in elimination or containment and/or via maintenance processes and/or via repair processes? I suggest distinguishing two situations here. The first situation corresponds to a dysfunctional immune system. An organism, either structurally or provisionally (e.g., after a treatment with immunosuppressive drugs), can have a defective immune system (e.g., a deficit in effector T cells, or a disequilibrium in the respective numbers of its inflammatory and regulatory macrophages – or, more specifically, of its macrophages distributed along the inflammatory to “alternatively activated” spectrum (Reference GordonGordon 2003; Reference Wynn, Chawla and PollardWynn et al. 2013)). Such abnormalities can contribute to explain the triggering of cancer, and they could be targeted by a number of therapies, which precisely aim at correcting these immune defects.

In the second situation, however, the immune system acts normally and immune-mediated decohesion is due to an abnormal context. Pathogens, wounds, mechanical pressure, and local modifications due to carcinogenic environmental factors, among several other causes, can create an abnormal local context (characterized by inflammation, perturbation of the extracellular matrix, and so on) (Reference Dolberg, Hollingsworth, Hertle and BissellDolberg et al. 1985; Reference Bissell and RadiskyBissell and Radisky 2001; Reference Mantovani, Allavena, Sica and BalkwillMantovani et al. 2008; Reference Fernández-Sánchez, Barbier and WhiteheadFernández-Sánchez et al. 2015). This local context influences the immune system, which in turn responds as it usually does, that is, by maintaining or repairing the tissue – even if the final, pathological, outcome is cancer promotion (Figure 4.4). It has long been known, for instance, that tumors resemble “wounds that do not heal” (Reference DvorakDvorak 1986, Reference Dvorak2015; Reference Schäfer and WernerSchäfer and Werner 2008), which means that, in cancer, normal repair mechanisms are triggered but generally without reaching the “resolution phase” (which, in the physiological context, is indispensable to terminate the reparative process (Reference Gurtner, Werner, Barrandon and LongakerGurtner et al. 2008)). Furthermore, the tumor itself can be a major source of perturbation of the local context: it can influence the immune system through a variety of cytokines and can also increase inflammation and wounding, modify blood vessels, reshape the extracellular matrix, or exert a mechanical pressure, among many other possibilities. This is often described as the “hijacking” or “co-option” by the tumor of physiological pathways and of the tissue microenvironment (Reference KitanoKitano 2004a; Reference GreavesGreaves 2007; Reference Lean and PlutynskiLean and Plutynski 2016). Despite its importance, one must keep in mind that such co-option is only one of the many ways in which the local context can become abnormal and favor the contribution of immune processes to cancer progression.

Figure 4.4

Decohesion in cancer induced by an abnormal context. Immune-mediated decohesion may be due to an abnormal context rather than an abnormal immune system. This abnormal context can be due to the presence of pathogens, wounds, mechanical pressures, and carcinogens of environmental origins, among many other resources; it can also be triggered by the tumor itself. In many situations, the decohesion mediated by the immune system results from abnormal realization of normal processes (such as maintenance and repair).

(Figure drawn by Wiebke Bretting).

In all these contexts, immune-mediated decohesion results from the abnormal realization of normal processes, and this can help explain why tumors largely resemble organs (Reference Egeblad, Nakasone and WerbEgeblad et al. 2010) and are the products of classic developmental (Reference da Costada Costa 2001; Reference Radisky, Hagios and BissellRadisky et al. 2001; Reference Huang, Ernberg and KauffmanHuang et al. 2009) and reparative pathways (Reference Bissell and RadiskyBissell and Radisky 2001) realized in an abnormal context. There is no doubt that the outcome is pathological (the promotion of a cancerous tumor, including in some cases metastatic spread), but the immune system, in many of these circumstances, does not strictly speaking “dysfunction”; it just does what it always does (maintaining the local environment, repairing in case of wound, etc.).

If the view presented here is correct, then a much richer picture emerges about how the immune system influences cancer and, ultimately, of potential therapeutic opportunities as well. Indeed, the immune system influences cancer through different processes (elimination, containment, maintenance, repair, and so on), via many actors (not only lymphocytes, but also macrophages, neutrophils, and various cytokines), at several different levels (within the tumor, but also around the tumor, in the whole tissue, and at a systemic level in the organism), and at all temporal stages of cancer progression (initiation, neoplastic progression, and metastasis). Additionally, the influence of the immune system on the cancerous tumor can be negative (the immune system prevents cancer progression) or positive (the immune system promotes cancer progression). All this suggests a whole series of new opportunities for investigating immunotherapies, which could, at least in principle, target these different processes, actors, levels, and temporal stages. Current immunotherapies (particularly immune checkpoint inhibitors and CAR-T cells (Reference Joyce and FearonJoyce and Fearon 2015; Reference June and SadelainJune and Sadelain 2018)) focus on lymphocytes in terms of actors and on elimination and maintenance and rupture of chronicity in terms of processes, but many other possibilities exist. Depending on where we are in the cycle of cancer–immune system interactions and on the actors of the tumor microenvironment involved, some therapeutic strategies will aim at normalization while others will aim at denormalization. Examples of normalization include the reduction of the level of inflammation in the tissue, the elimination of pathogens and/or chronic wounds, the restoration of immune accessibility to the tumor, and the facilitation of the resolving phase of tissue repair. In contrast, denormalization would be a major aim when the immune system interacts with tumor components as if they were normal constituents of the body, as, for example, when the immune system is tolerogenic in the context of chronically present tumor antigens or when the immune system continuously triggers repair pathways to respond to a local cancerous context that displays many features usually associated with a wound.

In summary, this section has shown that focusing on the immune system is essential for anyone studying cancer. Cancer is a disease of multicellularity and, more specifically, of the cohesion of the multicellular organism. Immunological surveillance constitutes one of the main and best described mechanisms by which the multicellular organism exerts control over lower-level entities. A major result of recent research is that the immune system can both restrain and promote cancerous tumors, which may seem, at first sight, paradoxical. Yet the situation becomes less paradoxical when one realizes that immune-mediated decohesion is often due to an abnormal context rather than a dysfunctional immune system. We have suggested here an extended view of cancer–immune interactions, which opens up many opportunities for investigating new mechanisms of tumor control and tumor promotion and, ultimately, for developing novel therapeutic opportunities based on the action of the immune system.

5.1 From Psychoneuroimmunology and Neuroimmunology to Present-Day Characterizations of the Dialogue between the Nervous and the Immune Systems

Despite important preexisting research on interactions between the nervous and the immune systems (relative to the blood–brain barrier, the idea of the brain as an immune-privileged organ, and the role of microglia cells, in particular; more will be said below about all these aspects), the fields of neuroimmunology and psychoneuroimmunology emerged in the 1970s and 1980s. The Neuroimmunology Branch of the National Institute of Neurological Disorders and Stroke was established in 1975 (Reference McFarland, Reich and JacobsonMcFarland et al. 2017). The journal Neuroimmunology was founded in 1981. Terms such as neuroinflammatory were already in use in the early 1980s (e.g., (Reference Hartung and ToykaHartung and Toyka 1983)). Psychoneuroimmunology was also born in the second half of the 1970s, following the work of Robert Ader (1932–2011) and a few others. The first edition of the volume Psychoneuroimmunology, edited by Ader, was published in 1981 (Reference AderAder 1981) and several updated editions followed. In 1987 Ader founded the journal Brain, Behavior, and Immunity, the official journal of the Psychoneuroimmunology Research Society. Importantly, the domain of psychoneuroimmunology stemmed in part from psychosomatic medicine (Reference Kiecolt-Glaser, McGuire, Robles and GlaserKiecolt-Glaser et al. 2002).Footnote ¹

Despite considerable overlap between neuroimmunology and psychoneuroimmunology, neuroimmunology tends to investigate the interactions between the nervous and the immune systems, particularly at the cellular and molecular levels, while psychoneuroimmunology explores how behavior influences and is influenced by the immune system. Historically, psychoneuroimmunology has focused on the conditioning of immune responses, the role of immune factors in mental disorders such as schizophrenia, and the effect of psychological factors such as stress on immune responses (Reference AderAder 2000). Later, the role of neuroimmune interactions in fatigue and sickness behavior (the feeling of fever and nausea, for example, when we are sick, and which is mediated by pro-inflammatory cytokines such as IL-1β) became important topics in the field (Reference Dantzer, O’Connor and FreundDantzer et al. 2008). As early as the 1970s, interactions under investigation included not just two but three actors: the nervous and the immune system, but also the endocrine system (Reference Besedovsky and SorkinBesedovsky and Sorkin 1977) (for a retrospective, see (Reference Besedovsky and ReyBesedovsky and Rey 2007)). This explains why some researchers talk about “psycho-neuro-endocrino-immunology” (Reference Sivik, Byrne and ChristodoulouSivik et al. 2002). Neuroimmunology, psychoneuroimmunology, and psycho-neuro-endocrino-immunology all pay attention to both the central nervous system (CNS) and the peripheral nervous system (PNS, the part of the nervous system that is outside the brain and spinal cord).

Strikingly, the fields of neuroimmunology and psychoneuroimmunology, since their inception, have given rise to controversies and have often been accused of not following the most rigorous scientific standards. This accusation has particularly targeted psychoneuroimmunology, as illustrated, for instance, by the disagreement between (Reference MaddoxMaddox 1984) and (Reference Ader and CohenAder and Cohen 1985), and as discussed in detail by (Reference CohenCohen 2006).

Here we will use neuroimmunology in an inclusive sense to refer to all the approaches nowadays that study interactions between the nervous and the immune system, at all levels, in health and disease, and with or without a focus on behavior.

5.2 Interactions between the Nervous and the Immune System in Health

Until the 1990s, a widespread conviction was that the brain was an “immuno-privileged” organ (Reference Carson, Doose and MelchiorCarson et al. 2006), understood as the idea that the brain is devoid of immune cells. The brain and the immune system were thought to be separated by a strict barrier, the blood–brain barrier (made of tightly packed endothelial cells, restricting the passage of many substances into the parenchyma), and the crossing of this barrier by immune cells was thought to be pathological and dangerous. Yet as with all other organs thought to be immuno-privileged (see Section 3), recent research has emphasized first that the brain has its own immune system, and second that the blood–brain barrier is partially permeable.

The main cellular actors of the brain immune system are microglia, the resident immune phagocytes of the CNS (see Figure 5.1). They constitute about 10 percent of the total cells in the adult CNS. Although microglia were documented as early as the 1920s, the conception of their roles and functioning has been considerably extended during the last decade (Reference Salter and BeggsSalter and Beggs 2014). In the healthy CNS, microglia, long conceived as dormant, are in fact highly active, continuously monitoring their environment with extremely motile processes and protrusions (Reference Nimmerjahn, Kirchhoff and HelmchenNimmerjahn et al. 2005) and interacting with neurons and other brain cells. Microglia initially were thought to simply react to CNS injury, infection, or pathology, but recent work suggests that they play a key role in synaptic remodeling both in development and in adult life, refining neuronal circuitry and network connectivity, and contributing to neuronal plasticity (Reference Wu, Dissing-Olesen, MacVicar and StevensWu et al. 2015). Importantly, the immune complement (Reference Stephan, Barres and StevensStephan et al. 2012) and the major histocompatibility complex class I molecule H2-D^b (Reference Lee, Brott and KirkbyLee et al. 2014) are also instrumental in CNS synapse pruning. Overall, microglia constitute a perfect illustration of what we described in Section 2, namely the fact that the activities of immune cells include but are not limited to defense, comprising also development, repair, clearance of debris, and so on (Reference Michell-Robinson, Touil and HealyMichell-Robinson et al. 2015).

Figure 5.1

Microglia and their many activities. Microglia are a major element of the brain’s immune system. These resident immune phagocytes constantly monitor their microenvironment and participate in many processes in health and disease, including engulfment of neural progenitor cells (NPCs), acute response to CNS damage, engulfment of synaptic material, and homeostatic surveillance.

(Figure drawn by Wiebke Bretting).

The long-dominant view has been that, in healthy conditions, the brain is devoid of lymphocytes, as these cells could cause major damage. Recently, however, a “peri-cerebral” adaptive immune system has been described (Figure 5.2): the meninges contain lymphatic vessels that remove waste from the parenchyma, can relay information about possible infections in the brain, but also harbor peripheral immune cells that communicate with the brain via cytokines (Reference Louveau, Smirnov and KeyesLouveau et al. 2015b; Reference KipnisKipnis 2016). This discovery confirms that there is a rich immunological crosstalk between the brain and the rest of the body, particularly via the meninges.

Figure 5.2

Immune communication between meninges and the brain. Apart from microglia, immune cells are generally not present in the brain, as, in nonpathological situations, they are thought to not cross the blood–brain barrier. However, meninges contain lymphatic vessels and peripheral immune cells, which communicate with the brain via cytokines.

(Figure drawn by Wiebke Bretting).

Collectively, these data confirm that there is a cellular and molecular immune system of the brain. The actors and mechanisms just described come in addition to various cell-intrinsic innate defense mechanisms used by neurons in case of viral infections (Reference Ordovas-Montanes, Rakoff-Nahoum and HuangOrdovas-Montanes et al. 2015).

Not only is there an immune system of the brain, but recent research confirms that there are many interactions between the nervous and the immune system in a healthy organism, with much richer communication pathways than initially suspected (Figure 5.3). These interactions occur at various levels: molecules, cells, organs, and at the systemic level. There is a dense sympathetic innervation of all lymphoid organs (Reference DantzerDantzer 2018). The PNS regulates immunological development (the sympathetic nervous system regulates haematopoiesis), priming (neurons influence the triggering of an immune response in lymph nodes), and deployment (peripheral neurons associated with vessels can impact on leukocyte recruitment into peripheral tissues) (Reference Ordovas-Montanes, Rakoff-Nahoum and HuangOrdovas-Montanes et al. 2015). In response to pathogens or tissue perturbation, immune cells are activated at the periphery and release cytokines and other inflammatory molecules; these molecules have an impact on local sensory neurons and influence signaling to the CNS (Reference Chavan, Pavlov and TraceyChavan et al. 2017). Furthermore, pro-inflammatory cytokines produced by immune cells at the periphery communicate with the brain through afferent nerves, a process that leads to the production (by activated microglia) of other pro-inflammatory mediators in the brain itself. (Using a perhaps slippery vocabulary, some authors say that the brain forms, via neuromediators and immune mediators, an “image” of immune responses occurring in peripheral tissues (Reference Dantzer, O’Connor and FreundDantzer et al. 2008)).

Figure 5.3

Communication between the nervous and the immune system. According to the initial view (top) neuroimmune interactions were thought to occur via neuroendocrine mediators released in the general circulation. According to the current view, however (down), long-distance interactions between the nervous and the immune system are mediated by neural pathways much more than by circulating neuroendocrine mediators, and the communication is bidirectional.

(Figure drawn by Wiebke Bretting, after Dantzer 2018).

Interactions between the nervous and the immune system can have important functional consequences. For example, homeostatic circuits regulating temperature maintenance, blood pressure, and intestinal mobility involve immune cells. The vagus nerve is important for detecting and reporting on peripheral immune responses and, in turn, efferent signals from the CNS are indispensable for the regulation of inflammatory responses (Reference Ordovas-Montanes, Rakoff-Nahoum and HuangOrdovas-Montanes et al. 2015). Kevin Tracey in the 2000s proposed calling this neuroimmune network the “inflammatory reflex” (reviewed in (Reference Chavan, Pavlov and TraceyChavan et al. 2017)), a concept enriched and discussed in subsequent research (Reference DantzerDantzer 2018).

Neuroimmune interactions can also involve additional actors. A major recent example is research on the microbiome–gut–brain axis. Mouse and insect models suggest that the microbiome influences brain development and behavior (Reference Sharon, Sampson, Geschwind and MazmanianSharon et al. 2016; Reference Vuong, Yano, Fung and HsiaoVuong et al. 2017; Reference Schretter, Vielmetter and BartosSchretter et al. 2018b), in part through the mediation of the immune system (Reference Fung, Olson and HsiaoFung et al. 2017). Whether this conclusion may apply to humans remains an open question.

Crucially, neuroimmune interactions have recently been said to have an impact on cognition. It has been proposed that cytokines play a critical role in spatial memory (Reference Sparkman, Buchanan and HeyenSparkman et al. 2006) and that microglia are important for learning and memory by promoting learning-related synapse formation through brain-derived neurotrophic factor signaling (Reference Parkhurst, Yang and NinanParkhurst et al. 2013). Furthermore, according to some authors, adaptive immunity influences cognition (Reference KipnisKipnis 2016). Mice deficient in T lymphocytes were found to exhibit cognitive impairment in spatial learning/memory tasks and passive transfer of mature T cells improves their cognitive function (Reference Kipnis, Cohen and CardonKipnis et al. 2004). A likely hypothesis is that pro-cognitive T cells are autoimmune cells stimulated by brain-derived molecular cues (Reference Kipnis, Gadani and DereckiKipnis et al. 2012). The influence of T cells on cognition could be mediated by interleukin-4 (IL-4), as the learning behavior of mice that do not express IL-4 is substantially lower than that of wild mice, and this effect can be reversed by injecting wild-type T cells but not T cells that do not express IL-4 (Reference Derecki, Cardani and YangDerecki et al. 2010). Another, nonexclusive, possibility is that this effect is mediated by myeloid cells. More recently, it has been claimed that mice deficient in adaptive immunity exhibit social deficits and hyperconnectivity of fronto-cortical brain regions, that social deficits are reversible via repopulation with lymphocytes, and that interferon-γ is a probable molecular link between meningeal immunity and neural circuits involved in social behavior (Reference Filiano, Xu and TustisonFiliano et al. 2016). Further work is needed to unravel the exact molecular and cellular mechanisms by which neuroimmune interactions affect cognition, but data accumulated in the last decade is highly promising and may open up new important avenues for research.

In summary, research in neuroimmunology over the last four decades has shown that there are many interactions between the nervous and the immune system. Neuroimmune interactions can be studied at different levels in the organism (from molecules to systems and even with an attention to environmental influences), at different scales (some neuroimmune communication pathways are short-distance, others are long-distance), and through an attention to different routes (direct interactions, but also indirect interactions, such as those involving endocrine elements or the microbiota).

5.3 Interactions between the Nervous and the Immune System in Pathological Contexts

According to some authors, neuroimmune interactions play a role not only in physiological but also in pathological contexts. Many disorders classically defined as neuronal and/or psychiatric are now said to possess a significant immunological component (Reference KipnisKipnis 2016). This is the case, for example, for some neurodegenerative disorders (Reference Heneka, Kummer and LatzHeneka et al. 2014) such as multiple sclerosis, which is an autoimmune disease (Reference Dendrou, Fugger and FrieseDendrou et al. 2015), but also in Alzheimer’s disease (Reference Heppner, Ransohoff and BecherHeppner et al. 2015). In addition, several lines of evidence suggest that various psychiatric pathologies could be caused, at least in part, by components of the immune system. Some authors emphasize that antineuronal autoantibodies are found in the serum of 11.6 percent of 925 patients admitted to acute psychiatric inpatient care (Reference Schou, Sæther and BorowskiSchou et al. 2016), others that 20 to 40 percent of acute psychiatric inpatients exhibit low-grade inflammation, suggesting the possibility that inflammation can be relevant for many psychiatric disorders (Reference Osimo, Cardinal, Jones and KhandakerOsimo et al. 2018) (as typically recognized for schizophrenia (Reference Khandaker, Cousins and DeakinKhandaker et al. 2015)). Many of these observations are limited and only correlative, so more work is needed to draw any conclusion here. An additional layer of complexity is that some autoimmune diseases such as lupus are accompanied with neuropsychiatric manifestations, which may be due to the existence of brain-reactive autoantibodies (Reference Williams, Sakic and HoffmanWilliams et al. 2010).

Several researchers propose that the immune system plays an important role in major depressive disorder. In humans, one-third of patients treated with cytokine therapies (IL-2 and IFN-α) for cancer or chronic viral hepatitis develop major depressive disorders (Reference Raison, Capuron and MillerRaison et al. 2006). Clinical observations, epidemiological studies, and investigations in animal models have tended to confirm that pro-inflammatory cytokines can induce depressive-like behaviors (Reference Dantzer, O’Connor and FreundDantzer et al. 2008). All this has contributed to the development of a non–brain-centric view of depression. The causal involvement of indoleamine 2,3-dioxygenase (IDO), an immune-inducible enzyme that metabolizes tryptophan along the kynurenine pathway and plays a major role in immunoregulation, was shown in animal models. Furthermore, pharmacological or genetic blockade of IDO activation abrogated depression-like behavior in mice (Reference DantzerDantzer 2018).

Collectively, these investigations on the role of neuroimmune interactions in psychiatric disorders have led to the emerging field of immunopsychiatry (Reference PariantePariante 2015). This domain has its origins in neuroimmunology and psychoneuroimmunology but focuses on the influence of immune mechanisms on behavior rather than the other way around.

If confirmed by future results, research on the role of the immune system in neurological and psychiatric diseases could have interesting and innovative therapeutic consequences. It has the potential to expand traditional approaches that see such diseases as purely mental and/or neurological, especially if future investigations confirm that some of these diseases can be managed via targeting of the immune system (among other components). This includes major depressive disorder (Reference Miller and RaisonMiller and Raison 2016; Reference BullmoreBullmore 2018), bipolar disorder, schizophrenia, and several others (Reference Miller and BuckleyMiller and Buckley 2017). The possibility to treat neurodegenerative disorders via immunotherapies also is under intense investigation (Reference Weiner and FrenkelWeiner and Frenkel 2006).

Interestingly, an immunological approach could lead to redefined nomenclatures of psychiatric disorders and treatments. Diagnosis for psychiatric disorders is currently based on descriptive nomenclature because of a lack of clearly defined causal mechanisms. Yet some immunological mechanisms are common to psychiatric disorders belonging to different categories, hence the suggestion to develop alternative nomenclatures based on immunological characteristics as well as associated environmental factors (Reference Leboyer, Berk and YolkenLeboyer et al. 2016).

Reciprocally, some diseases traditionally classified as immune may be targeted by acting on the nervous system. For example, in a recent clinical study, electrical vagus nerve stimulation was successfully used to improve symptoms in rheumatoid arthritis, a chronic inflammatory and autoimmune disease (Reference Koopman, Chavan and MiljkoKoopman et al. 2016). Further investigations are needed, but some specialists consider that bioelectronic devices can be used to modulate neural circuitries, constituting a complement to drug treatment, especially in immune diseases (Reference Chavan, Pavlov and TraceyChavan et al. 2017)

The field of immunotherapy-based approaches to neurological and psychiatric diseases is still in its infancy. Yet if successful, it could contribute to closing the gap between psychiatry and the rest of medicine, and it could lead to a radical change in the way we traditionally conceive mental health problems.

5.4 Mapping the Different Conceptual Questions Raised by Neuroimmunology

Recent scientific literature abounds in bold claims about the relation between the nervous and the immune system. These two systems are often said to have strong interactions and many similarities, perhaps a common evolutionary origin, while some suggest that they overlap to a great extent and even that they could constitute a single system (see details below). I suggest that, even if several of such claims are often formulated as if they were intimately connected or even equivalent, it is crucial, for the sake of clarity, to disentangle these claims. My analysis of this literature has led me to single out five dimensions of neuroimmunology, each corresponding to a different question (Figure 5.4): interaction, similarity, overlap, origins, and control. Importantly, distinguishing five questions in neuroimmunology can serve not only as a mapping of the various goals currently pursued by researchers in this domain but also as an invitation to do further investigations to better address some questions that have tended to remain in the background in the last two decades.

Figure 5.4

Neuroimmunology: A conceptual tree. This figure distinguishes five different questions raised by current scientific literature in neuroimmunology, and which in general are insufficiently separated.

5.5 Conclusion: Some Philosophical Consequences

Let’s end this section by drawing three philosophical consequences from this exploration of neuroimmunology. First, neuroimmunology offers useful (although not unique) lessons about interdisciplinarity. Two types of interdisciplinarity are found in neuroimmunology: horizontal (integration of different disciplines – here neurobiology and immunology, to which one must actually add endocrinology and psychology) and vertical (integration of different levels of analysis, from molecules to systems, pertaining traditionally to distinct domains). Neuroimmunology also illustrates exemplarily the well-known fact that disciplines create mindsets and even norms of judgement and action. These mindsets are difficult to overcome in basic research as well as in the clinic. For example, few immunologists think about using neurostimulation to cure patients with autoimmune diseases, and until recently few psychiatrists considered using immune-based therapies to treat mental disorders. In addition to such epistemological questions, interdisciplinarity in neuroimmunology raises an ontological question: are there really three systems (nervous, immune, endocrine) in animals like us, or, as suggested, for example, by (Reference SteinmanSteinman 2012), are those only projections of our thought and language on the world? Personally, I see the epistemological issue as more stimulating and pressing than the ontological one, but both may converge to a large extent.

Second, what has been said here confirms the importance of adopting an extended view of immunity, as argued in the previous sections. In the context of neuroimmunology this extension has two dimensions. The first dimension has to do with the diversity of activities achieved by the immune system. To the various immunological activities already identified in the previous sections (development, clearance of debris, repair, and so on) one must add that the immune system could also influence the nervous system and cognitive functions. The second dimension is that the immune system is extended in another sense, namely insofar as it is connected with other systems (here the nervous and endocrine systems) and sometimes overlaps with them.

Third, our discussion suggests that immunology makes a significant contribution to the understanding of behavior and cognition and should therefore attract the attention of philosophers of neuroscience and philosophers of cognitive science. If the experimental results presented above are correct, then the immune system influences various feelings, behaviors, and cognitive processes either directly or indirectly (through its interactions with the CNS, PNS, endocrine system, and/or other systems). The immune system has an impact on sickness behavior (Reference Konsman, Parnet and DantzerKonsman et al. 2002) and major depressive disorder (Reference DantzerDantzer 2018), and strategies are currently being developed to treat several behavioral disorders by targeting the immune system. Another major example is pain, a highly discussed topic in the philosophy of the neurosciences (Reference HardcastleHardcastle 1997) and in general philosophy as well. Activated immune cells release pro-inflammatory cytokines, which sensitize sensory nerve endings, leading to an amplification and prolongation of pain; but the pain response also is downregulated via opioid-containing immune cells, as these cells release opioid peptides, which interact with opioid receptors on sensory nerves (Reference Stein, Hassan and PrzewłockiStein et al. 1990). All this corroborates the claim that pain is a highly complex process with several feedback loops and involving several bodily systems (Reference HardcastleHardcastle 1997). Last but not least, many researchers propose that the immune system, via microglia, T cells, and cytokines, participates in cognition, particularly in learning and spatial memory.

All these data contribute to question brain-centered and more generally nervous system–centered views of behavior and cognition. Clearly, the nervous system remains crucial in all the processes described above, but it would nonetheless be inadequate to consider only the nervous system when trying to identify the biological basis of feelings, emotions, behaviors, and cognitive states. Understanding these processes requires an integrative approach in which the immune system could play an important role. Accordingly, neuroimmunology lends more weight to the idea of embodied cognition, that is, the idea that bodily elements distinct from the brain play a significant role in cognitive processing (Reference ShapiroShapiro 2010). It also offers additional arguments to those who emphasize the importance of interoception (Reference CraigCraig 2002) insofar as it suggests that the brain can form a representation of the immunological status of peripheral tissues.

One may wonder, though, whether the immune system is an essential component of behavior and cognition. Here the answer will depend on what exactly is meant by this question. If the question is whether the immune system could influence behavior and cognition on its own, that is, independently of the (central and peripheral) nervous system, then the answer is probably negative. But if the question is whether the immune system is essential for proper functioning of the nervous system in some behavioral and cognitive activities, then the answer is affirmative, as exemplarily illustrated by microglia-mediated synaptic remodeling. More specifically, I suggest that the immune system can play three kinds of specific roles that are essential for the functioning of the nervous system and particularly for the realization of some cognitive processes. First, the immune system is an informant for the nervous system. It provides vital information about infections, damage, and other perturbations that occur in any part of the organism. If, as proposed in Section 2, the capacity to respond to pathogens and other sources of damage constitutes one of the strongest evolutionary pressures on organisms, then conveying information to the nervous system about the immunological status of the host is vital. Second, the immune system is an executant for the nervous system: it realizes distinctive activities indispensable for the functioning of the nervous system, such as elimination of dead cells, repair, and so on. Third, and most crucially, the immune system is a messenger for the nervous system: not only does the nervous system resort to the molecular communication pathways of the immune system (cytokines) but it makes use of the unique feature of immune cells, namely their mobility, which allows them to reach any part of the organism and to deliver complex messages there. I suspect that, in coming years, cognitive functions mediated by this unique mobility of immune cells will be uncovered.

Current research in neuroimmunology raises other philosophically interesting issues, which could not be examined here due to space restrictions. These include how the nervous and the immune system interact in the construction of biological individuality and rethinking central physiological concepts such as homeostasis in light of the crosstalk between these two systems, among many other questions. Again, the aim of this section was simply to convince the reader that neuroimmunology is full of philosophical promise.