Skip to main content Accessibility help
×
Hostname: page-component-848d4c4894-nr4z6 Total loading time: 0 Render date: 2024-05-17T15:46:04.026Z Has data issue: false hasContentIssue false

Chapter 16 - Gene Therapy in Fetal Growth Restriction

from Section 4 - Prophylaxis and Treatment

Published online by Cambridge University Press:  23 July 2018

Christoph Lees
Affiliation:
Imperial College London
Gerard H. A. Visser
Affiliation:
Universiteit Utrecht, The Netherlands
Kurt Hecher
Affiliation:
University Medical Centre, Hamburg
Get access

Summary

Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2018

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

David, AL, Peebles, D. Gene therapy for the fetus: Is there a future? Best Pract Res Clin Obstet Gynaecol 2008;22(1):203–18.Google Scholar
Mattar, CN, Waddington, SN, Biswas, A, Davidoff, AM, Choolani, M, Chan, JKY, et al. The case for intrauterine gene therapy. Best Pract Res Clin Obstet Gynaecol 2012;26(5):697709.CrossRefGoogle ScholarPubMed
Gene Therapy Advisory Committee. Report on the potential use of gene therapy in utero. Health Departments of the United Kingdom, November 1998. Hum Gene Ther 1999;10(4):689–92.Google Scholar
U. S. National Institutes of Health. Recombinant DNA Advisory Committee. Prenatal gene transfer: Scientific, medical, and ethical issues: A report of the Recombinant DNA Advisory Committee. Hum Gene Ther 2000;11(8):1211–29.Google Scholar
Lyall, F, Robson, SC, Bulmer, JN. Spiral artery remodeling and trophoblast invasion in preeclampsia and fetal growth restriction: Relationship to clinical outcome. Hypertension 2013;62(6):1046–54.CrossRefGoogle ScholarPubMed
Konje, JC, Howarth, ES, Kaufmann, P, Taylor, DJ. Longitudinal quantification of uterine artery blood volume flow changes during gestation in pregnancies complicated by intrauterine growth restriction. BJOG 2003;110(3):301–5.Google Scholar
Ginn, SL, Alexander, IE, Edelstein, ML, Abedi, MR, Wixon, J. Gene therapy clinical trials worldwide to 2012 – an update. J Gene Med 2013;15(2):6577.Google Scholar
Coutelle, C, Waddington, SN. Vector systems for prenatal gene therapy: Choosing vectors for different applications. Methods Mol Biol 2012;891:4153.Google Scholar
Khare, R, Chen, CY, Weaver, EA, Barry, MA. Advances and future challenges in adenoviral vector pharmacology and targeting. Curr Gene Ther 2011;11(4):241–58.CrossRefGoogle ScholarPubMed
Katayama, K, Furuki, R, Yokoyama, H, Kaneko, M, Tachibana, M, Yoshida, I, et al. Enhanced in vivo gene transfer into the placenta using RGD fiber-mutant adenovirus vector Biomaterials 2011;32(17):4185–93.CrossRefGoogle ScholarPubMed
Al-Hendy, A, Salama, S. Gene therapy and uterine leiomyoma: A review. Hum Reprod Update 2006;12(4):385400.CrossRefGoogle ScholarPubMed
Stribley, JM, Rehman, KS, Niu, H, Christman, GM. Gene therapy and reproductive medicine. Fertil Steril 2002;77(4):645–57.CrossRefGoogle ScholarPubMed
Ahmed, A, Dunk, C, Ahmad, S, Khaliq, A. Regulation of placental vascular endothelial growth factor (VEGF) and placenta growth factor (PIGF) and soluble Flt-1 by oxygen – a review. Placenta 2000;21 Suppl A:S16–24.CrossRefGoogle ScholarPubMed
Olsson, AK, Dimberg, A, Kreuger, J, Claesson-Welsh, L. VEGF receptor signalling – in control of vascular function. Nat Rev Mol Cell Biol 2006;7(5):359–71.Google Scholar
Savvidou, MD, Yu, CK, Harland, LC, Hingorani, AD, Nicolaides, KH. Maternal serum concentration of soluble fms-like tyrosine kinase 1 and vascular endothelial growth factor in women with abnormal uterine artery Doppler and in those with fetal growth restriction. Am J Obstet Gynecol 2006;195(6):1668–73.Google Scholar
Herraiz, I, Droge, LA, Gomez-Montes, E, Henrich, W, Galindo, A, Verlohren, S. Characterization of the soluble fms-like tyrosine kinase-1 to placental growth factor ratio in pregnancies complicated by fetal growth restriction. Obstet Gynecol 2014;124(2 Pt 1):265–73.CrossRefGoogle ScholarPubMed
Roberts, CT, Owens, JA, Sferruzzi-Perri, AN. Distinct actions of insulin-like growth factors (IGFs) on placental development and fetal growth: Lessons from mice and guinea pigs. Placenta 2008;29 Suppl A:S42–7.CrossRefGoogle ScholarPubMed
Forbes, K, Westwood, M. The IGF axis and placental function. A mini review. Horm Res 2008; 69(3):129–37.Google Scholar
David, AL, Torondel, B, Zachary, I, Wigley, V, Abi-Nader, K, Mehta, V, et al. Local delivery of VEGF adenovirus to the uterine artery increases vasorelaxation and uterine blood flow in the pregnant sheep. Gene Ther 2008;15(19):1344–50.Google Scholar
Mehta, V, Abi-Nader, KN, Peebles, DM, Benjamin, E, Wigley, V, Torondel, B, et al. Long-term increase in uterine blood flow is achieved by local overexpression of VEGF-A(165) in the uterine arteries of pregnant sheep. Gene Ther 2012;19(9):925–35.CrossRefGoogle ScholarPubMed
Mehta, V, Abi-Nader, KN, Shangaris, P, Shaw, SW, Filippi, E, Benjamin, E, et al. Local over-expression of VEGF-DDeltaNDeltaC in the uterine arteries of pregnant sheep results in long-term changes in uterine artery contractility and angiogenesis. PloS One 2014; 9(6):e100021.Google Scholar
Wallace, JM, Luther, JS, Milne, JS, Aitken, RP, Redmer, DA, Reynolds, LP, et al. Nutritional modulation of adolescent pregnancy outcome – a review. Placenta 2006;27 Suppl A:S61–8.Google Scholar
Robinson, JS, Kingston, EJ, Jones, CT, Thorburn, GD. Studies on experimental growth retardation in sheep. The effect of removal of a endometrial caruncles on fetal size and metabolism. J Dev Physiol 1979; 1(5):379–98.Google Scholar
Wallace, JM, Aitken, RP, Milne, JS, Hay, WW, Jr. Nutritionally mediated placental growth restriction in the growing adolescent: Consequences for the fetus. Biol Reprod 2004;71(4):1055–62.Google Scholar
Wallace, JM, Milne, JS, Matsuzaki, M, Aitken, RP. Serial measurement of uterine blood flow from mid to late gestation in growth restricted pregnancies induced by overnourishing adolescent sheep dams. Placenta 2008;29(8):718–24.Google Scholar
Wallace, JM, Bourke, DA, Aitken, RP, Palmer, RM, Da, Silva, P, Cruickshank, MA. Relationship between nutritionally-mediated placental growth restriction and fetal growth, body composition and endocrine status during late gestation in adolescent sheep. Placenta 2000;21(1):100–8.Google Scholar
Carr, DJ, Aitken, RP, Milne, JS, David, AL, Wallace, JM. Fetoplacental biometry and umbilical artery Doppler velocimetry in the overnourished adolescent model of fetal growth restriction. Am J Obstet Gynecol 2012; 207(2):141.Google Scholar
Redmer, DA, Aitken, RP, Milne, JS, Reynolds, LP, Wallace, JM. Influence of maternal nutrition on messenger RNA expression of placental angiogenic factors and their receptors at midgestation in adolescent sheep. Biol Reprod 2005;72(4):1004–9.CrossRefGoogle ScholarPubMed
Redmer, DA, Luther, JS, Milne, JS, Aitken, RP, Johnson, ML, Borowicz, PP, et al. Fetoplacental growth and vascular development in overnourished adolescent sheep at day 50, 90 and 130 of gestation. Reproduction 2009;137(4):749–57.CrossRefGoogle ScholarPubMed
Lea, RG, Wooding, P, Stewart, I, Hannah, LT, Morton, S, Wallace, K, et al. The expression of ovine placental lactogen, StAR and progesterone-associated steroidogenic enzymes in placentae of overnourished growing adolescent ewes. Reproduction 2007; 133(4):785–96.Google Scholar
Carr, DJ, Aitken, RP, Milne, JS, David, AL, Wallace, JM. Ultrasonographic assessment of growth and estimation of birthweight in late gestation fetal sheep. Ultrasound Med Biol 2011;37(10):1588–95.Google Scholar
Smith, GC, Smith, MF, McNay, MB, Fleming, JE. The relation between fetal abdominal circumference and birthweight: Findings in 3512 pregnancies. BJOG 1997;104(2):186–90.CrossRefGoogle ScholarPubMed
Carr, DJ, Aitken, RP, Milne, JS, Peebles, DM, Martin, JM, Zachary, IC, et al. Prenatal Ad.VEGF gene therapy – a promising new treatment for fetal growth restriction. Hum Gene Ther 2011;22(10):A128.Google Scholar
Carr, DJ, Aitken, RP, Milne, JS, Peebles, DM, Martin, JM, Zachary, IC, et al. Maternal delivery of Ad.VEGF gene therapy increases fetal growth velocity in an ovine paradigm of fetal growth restriction. Reprod Sci 2011; 18(3 suppl):269A.Google Scholar
Carr, DJ, Aitken, RP, Milne, JS, Peebles, DM, Martin, JM, Zachary, IC, et al. Alterations in postnatal growth and metabolism following prenatal treatment of intrauterine growth restriction with Ad.VEGF gene therapy in the sheep. Arch Dis Child Fetal Neonatal Ed 2011;96:Fa7.CrossRefGoogle Scholar
Carr, DJ, Aitken, RP, Milne, JS, Peebles, DM, Martin, JF, Zachary, IC, et al. Prenatal gene therapy increases fetal growth velocity and expression of VEGF receptors in an ovine paradigm of fetal growth restriction. Reprod Sci 2012;19(3):78A.Google Scholar
Carter, AM. Animal models of human placentation – a review. Placenta 2007;28 Suppl A:S41–7.CrossRefGoogle ScholarPubMed
Mess, A. The Guinea pig placenta: Model of placental growth dynamics. Placenta 2007;28(8–9):812–15.CrossRefGoogle ScholarPubMed
Roberts, CT, Sohlstrom, A, Kind, KL, Earl, RA, Khong, TY, Robinson, JS, et al. Maternal food restriction reduces the exchange surface area and increases the barrier thickness of the placenta in the guinea-pig. Placenta 2001;22(2–3):177–85.Google Scholar
Mehta, V, Boyd, M, Martin, J, Zachary, I, Peebles, DM, David, AL. Local administration of Ad.VEGF-A165 to the uteroplacental circulation enhances fetal growth and reduces brain sparing in an FGR model of guinea pig pregnancy. Reprod Sci 2012;19(3):78A.Google Scholar
Sferruzzi-Perri, AN, Owens, JA, Pringle, KG, Robinson, JS, Roberts, CT. Maternal insulin-like growth factors-I and -II act via different pathways to promote fetal growth. Endocrinology 2006;147(7):3344–55.CrossRefGoogle ScholarPubMed
Sferruzzi-Perri, AN, Owens, JA, Standen, P, Taylor, RL, Heinemann, GK, Robinson, JS, et al. Early treatment of the pregnant guinea pig with IGFs promotes placental transport and nutrient partitioning near term. Am J Physiol Endocrinol Metab 2007;292(3):E668–76.Google Scholar
Sohlstrom, A, Fernberg, P, Owens, JA, Owens, PC. Maternal nutrition affects the ability of treatment with IGF-I and IGF-II to increase growth of the placenta and fetus, in guinea pigs. Growth Horm IGF Res 2001; 11(6):392–8.Google Scholar
Eremia, SC, de Boo, HA, Bloomfield, FH, Oliver, MH, Harding, JE. Fetal and amniotic insulin-like growth factor-I supplements improve growth rate in intrauterine growth restriction fetal sheep. Endocrinology 2007;148(6):2963–72.Google Scholar
Wali, JA, de Boo, HA, Derraik, JG, Phua, HH, Oliver, MH, Bloomfield, FH, et al. Weekly intra-amniotic IGF-1 treatment increases growth of growth-restricted ovine fetuses and up-regulates placental amino acid transporters. PloS One 2012;7(5):e37899.CrossRefGoogle ScholarPubMed
Miller, AG, Aplin, JD, Westwood, M. Adenovirally mediated expression of insulin-like growth factors enhances the function of first trimester placental fibroblasts. J Clin Endocrinol Metab 2005; 90(1):379–85.Google Scholar
Jones, H, Crombleholme, T, Habli, M. Regulation of amino acid transporters by adenoviral-mediated human insulin-like growth factor-1 in a mouse model of placental insufficiency in vivo and the human trophoblast line BeWo in vitro. Placenta 2014; 35(2):132–8.Google Scholar
Jones, HN, Crombleholme, T, Habli, M. Adenoviral-mediated placental gene transfer of IGF-1 corrects placental insufficiency via enhanced placental glucose transport mechanisms. PloS One 2013;8(9):e74632.Google Scholar
Habli, M, Jones, H, Aronow, B, Omar, K, Crombleholme, TM. Recapitulation of characteristics of human placental vascular insufficiency in a novel mouse model. Placenta 2013;34(12):1150–8.Google Scholar
David, AL, Ashcroft, R. Placental gene therapy. Obstet Gynaecol Reprod Med 2009;19(10):296–8.Google Scholar
Sheppard, MK, Spencer, RN, David, AL, Ashcroft, R. Evaluation of the ethics and social acceptability of a proposed clinical trial using maternal gene therapy to treat severe early-onset fetal growth restriction in pregnant women. Hum Gene Ther 2014:A98.Google Scholar
Hedman, M, Muona, K, Hedman, A, Kivela, A, Syvanne, M, Eranen, J, et al. Eight-year safety follow-up of coronary artery disease patients after local intracoronary VEGF gene transfer. Gene Ther 2009; 16(5):629–34.Google Scholar
Rosengart, TK, Bishawi, MM, Halbreiner, MS, Fakhoury, M, Finnin, E, Hollmann, C, et al. Long-term follow-up assessment of a phase 1 trial of angiogenic gene therapy using direct intramyocardial administration of an adenoviral vector expressing the VEGF121 cDNA for the treatment of diffuse coronary artery disease. Hum Gene Ther 2013;24(2):203–8.CrossRefGoogle ScholarPubMed
Heikkila, A, Hiltunen, MO, Turunen, MP, Keski-Nisula, L, Turunen, AM, Rasanen, H, et al. Angiographically guided utero-placental gene transfer in rabbits with adenoviruses, plasmid/liposomes and plasmid/polyethyleneimine complexes. Gene Ther 2001; 8(10):784–8.Google Scholar
Brownbill, P, Desforges, M, Sebire, N, Greenwood, S, Sibley, CP, David, A. Human placental ex vivo studies to support an adenovirus-mediated vascular endothelial growth factor (VEGF) gene medicine for the treatment of severe early onset fetal growth restriction (FGR). Hum Gene Ther 2014;25(11):A60.Google Scholar
Woo, YJ, Raju, GP, Swain, JL, Richmond, ME, Gardner, TJ, Balice-Gordon, RJ. In utero cardiac gene transfer via intraplacental delivery of recombinant adenovirus. Circulation 1997;96(10):3561–9.Google Scholar
Turkay, A, Saunders, T, Kurachi, K. Intrauterine gene transfer: Gestational stage-specific gene delivery in mice. Gene Ther 1999;6(10):1685–94.CrossRefGoogle ScholarPubMed
Xing, A, Boileau, P, Cauzac, M, Challier, JC, Girard, J, Hauguel-de Mouzon, S. Comparative in vivo approaches for selective adenovirus-mediated gene delivery to the placenta. Hum Gene Ther 2000; 11(1):167–77.CrossRefGoogle ScholarPubMed
Senoo, M, Matsubara, Y, Fujii, K, Nagasaki, Y, Hiratsuka, M, Kure, S, et al. Adenovirus-mediated in utero gene transfer in mice and guinea pigs: tissue distribution of recombinant adenovirus determined by quantitative TaqMan-polymerase chain reaction assay. Mol Genet Metab 2000;69(4):269–76.CrossRefGoogle ScholarPubMed
Katz, AB, Keswani, SG, Habli, M, Lim, FY, Zoltick, PW, Midrio, P, et al. Placental gene transfer: Transgene screening in mice for trophic effects on the placenta. Am J Obstet Gynecol 2009;201(5):499.e1–8.Google Scholar
Mehta, V, Peebles, DM, Boyd, M, Zachary, I, Martin, J, David, AL. Gene targeting to the utero-placental circulation of pregnant guinea pigs. Society for Gynaecologic Investigation 58th Annual Meeting: Reproductive Sciences; 2011. p. 332A.Google Scholar
Mok, M, Heidemann, B, Dundas, K, Gillespie, I, Clark, V. Interventional radiology in women with suspected placenta accreta undergoing caesarean section. Int J Obstet Anesth 2008;17(3):255–61.Google Scholar
Carnevale, FC, Kondo, MM, de Oliveira Sousa, W, Jr., Santos, AB, da Motta Leal Filho, JM, Moreira, AM, et al. Perioperative temporary occlusion of the internal iliac arteries as prophylaxis in cesarean section at risk of hemorrhage in placenta accreta. Cardiovasc Intervent Radiol 2011;34(4):758–64.Google Scholar
Alfirevic, Z, Sundberg, K, Brigham, S. Amniocentesis and chorionic villus sampling for prenatal diagnosis. Cochrane Database Syst Rev 2003(3):CD003252.Google Scholar
Wing, DA, Powers, B, Hickok, D. U.S. Food and Drug Administration drug approval: Slow advances in obstetric care in the United States. Obstet Gynecol 2010;115(4):825–33.Google Scholar
European Medicines Agency. Guideline on the Non-clinical Studies Required before First Clinical Use of Gene Therapy Medicinal Products (EMEA/CHMP/GTWP/125459/2006). London: European Medicines Agency; 2008.Google Scholar
European Medicines Agency. ICH Harmonised Tripartite Guideline E6: Note for Guidance on Good Clinical Practice (PMP/ICH/135/95). London: European Medicines Agency; 2002.Google Scholar
European Medicines Agency. Detection of Toxicity to Reproduction for Medicinal Products and Toxicity to Male Fertility (CPMP/ICH/386/95). London: European Medicines Agency; 1994.Google Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×