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Assessment of early and post COVID-19 vaccination antibody response in healthcare workers: a multicentre cross-sectional study on inactivated, mRNA and vector-based vaccines

Published online by Cambridge University Press:  05 January 2023

Roxana Mansour Ghanaie
Affiliation:
Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Mahnaz Jamee
Affiliation:
Pediatric Nephrology Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Hannan Khodaei
Affiliation:
Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Armin Shirvani
Affiliation:
Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran School of Management and Medical Education Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Arezu Amirali
Affiliation:
Department of Microbiology, Faculty of Biological Sciences, Alzahra University, Tehran, Iran
Abdollah Karimi
Affiliation:
Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Fatemeh Fallah
Affiliation:
Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Leila Azimi
Affiliation:
Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Shahnaz Armin
Affiliation:
Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Seyed Alireza Fahimzad
Affiliation:
Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Sedigheh Rafiei Tabatabaei
Affiliation:
Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Zari Gholinegad
Affiliation:
Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Maryam Rajabnejad
Affiliation:
Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Marzieh Moemeni
Affiliation:
Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Maryam Kazemi Aghdam
Affiliation:
Pediatric Pathology Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Shamsollah Noripour
Affiliation:
Neonatal Health Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Mandana Mansour Ghanaie
Affiliation:
Reproductive Health Research Center, Department of Obstetrics and Gynecology, Alzahra Hospital, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran
Marjan Tariverdi
Affiliation:
Department of Pediatrics, Clinical Research Development Center of Children Hospital, Hormozgan University of Medical Sciences, Bandar Abbas, Iran
Mohammadreza Soroush
Affiliation:
Nikan Education and Research Center, Tehran, Iran
Mahdi Masomi
Affiliation:
Nikan Education and Research Center, Tehran, Iran
Fereshteh Shahraki
Affiliation:
Nikan Education and Research Center, Tehran, Iran
Sharif Torkaman-Nejad
Affiliation:
Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Soheila Sadat Vaghefi
Affiliation:
Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Fariba Shirvani
Affiliation:
Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Masoud Alebouyeh*
Affiliation:
Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran
*
Author for correspondence: Masoud Alebouyeh, E-mail: masoud.alebouyeh@gmail.com
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Abstract

In this multicentre study, we compared the status of antibody production in healthcare personnel (HCP) before and after vaccination using different brands of COVID-19 vaccines between March 2021 and September 2021. Out of a total of 962 HCP enrolled in our study, the antibody against the S1 domain of SARS-CoV-2 was detected in 48.3%, 95.5% and 96.2% of them before, after the first and the second doses of the vaccines, respectively. Our results showed post-vaccination infection in 3.7% and 5.9% of the individuals after the first and second doses of vaccines, respectively. The infection was significantly lower in HCP who presented higher antibody titres before the vaccination. Although types of vaccines did not show a significant difference in the infection rate, a lower infection rate was recorded for AstraZeneca after the second vaccination course. This rate was equal among individuals receiving a second dose of Sinopharm and Sputnik. Vaccine-related side effects were more frequent among AstraZeneca recipients after the first dose and among Sputnik recipients after the second dose. In conclusion, our results showed diversity among different brands of COVID-19 vaccines; however, it seems that two doses of the vaccines could induce an antibody response in most of HCP. The induced immunity could persist for 3–5 months after the second vaccination course.

Type
Original Paper
Creative Commons
Creative Common License - CCCreative Common License - BYCreative Common License - NCCreative Common License - SA
This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike licence (http://creativecommons.org/licenses/by-nc-sa/4.0), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the same Creative Commons licence is used to distribute the re-used or adapted article and the original article is properly cited. The written permission of Cambridge University Press must be obtained prior to any commercial use.
Copyright
Copyright © The Author(s), 2023. Published by Cambridge University Press

Introduction

The humoral immune response plays a prominent role in fighting against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and protection against re-infection [Reference Sharma1]. Antibodies to SARS-CoV-2 are detectable approximately 2 weeks after the onset of symptoms and can persist for at least 6 months [Reference Gaebler2]. Evaluation of the immune response following a SARS-CoV-2 infection and vaccination can provide a valuable tool in determining the nature of the unprecedented pandemic we are facing and can indicate the rate of disease transmission over time [Reference Jackson-Thompson3].

COVID-19, first detected in December 2019 in Wuhan, China, has rapidly become a global pandemic affecting 498 704 919 people as on 10 April 2022, and claiming the life of 6 202 473 people worldwide [4]. Among other entities, healthcare workers (HCWs) are potentially at high risk for SARS-CoV-2 infection due to the direct contact with COVID-19-positive patients and also due to community exposure.

The clinical manifestations of COVID-19 range widely from asymptomatic infection to severe life-threatening multi-organ failure [Reference He5]. There are concerns that, compared to the general population, many HCWs seem to acquire SARS-CoV-2 infection in an asymptomatic or mildly symptomatic manner. As a result, the infection may not be detected early in the course of the disease, making them act as silent spreaders [Reference Self6, Reference Menon7]. There is currently a paucity of information on the pre- and post-vaccination COVID-19 seroprevalence among HCWs. The prevalence of antibody seropositivity in the pre-vaccination era among Iranian general and high-risk populations was estimated as 17.1% and 20.0%, respectively [Reference Poustchi8]. Although the vaccination for Iranian HCWs began around March 2021, the seroprevalence after receiving vaccination among HCWs has not been yet investigated. In addition, the impact of COVID-19 onset and/or administration of available vaccines on protection against re-infection and the so effects of different types and dosages of vaccines on the induction of neutralising antibodies and conferring alleviation of symptom severity in case of re-infection are not completely clear.

To investigate the effect of protective proceedings, such as vaccinations, on the induction of antibodies and the occurrence of the disease, HCWs can be the optimal population, as they were the first population to receive vaccines and are encountering the SARS-CoV-2-infected patients. In this regard, we aim to evaluate the prevalence of and factors associated with SARS-CoV-2 infection among frontline and non-frontline HCWs regarding the induced antibodies after natural infection and SARS-CoV-2 vaccination with different brands. A possible correlation between antibody response to different brands of the vaccines with age, body mass index (BMI), gender and history of infection was also analysed in this population.

Materials and methods

Study design

This prospective multicentre cross-sectional study was designed to determine the proportion of SARS-CoV-2 infection in healthcare personnel (HCP) of three hospitals in Iran from 2020 to 2021. In this study, the WHO COVID-19 protocol was followed (WHO/2019-nCoV/HCW_Surveillance_Protocol/2020.1). A questionnaire was used based on the WHO protocol regarding the general demographic information and questions for COVID-19 infection, such as brands and time of vaccination, exposure history with COVID-19 patients and confirmed infection using polymerase chain reaction (PCR) tests. HCW from different disciplines, including those in the patients' room and those who were indirectly in contact with contaminated materials and the environment, were included in the study in these hospitals. Blood samples were obtained from all HCWs who signed the consent form, and the specimens were sent to the central laboratory for processing and storage. All the serum samples were stored at −70 °C until use for serological assay. The study was approved by the ethical committee of Shahid Beheshti University of Medical Sciences, Tehran, Iran (Code: IR.SBMU.RICH.REC.1399.066).

Sampling and enzyme-linked immunosorbent assay (ELISA)

The blood samples were obtained by venepuncture and transferred into serum separator gel tubes. To separate sera in microcentrifugation tube, centrifugation on 80 000 rpm for 10 min was done. The separated sera were pour into 1.5 ml microtubes and stored them at −70 °C until used for ELISA. To measure infection with SARS-CoV-2, immunoglobulin G (IgG) antibody against the S1 domain of SARS-CoV-2 spike protein was measured using an anti-SARS-CoV-2 IgG antibody kit (Euroimmun, Germany). To calculate the ratio of the antibody in each sample, absorbance on 450/620 nm compared with the calibrator was measured. Interpretation of results was done according to the manufacturer's instructions. Accordingly, ratios equal to and over 1.1 were considered positive, those ≥0.8≤1.1 as borderline and those lower than 0.8 as negative. The collected samples with either positive or borderline results were rechecked with the WANTAI SARS-CoV-2 Ab ELISA kit according to the manufacturer's instructions (WANTAI BioPharm, China).

Statistical analysis

SPSS software was used for statistical analysis. Accordingly, logistic regression analysis was performed to evaluate the effect of factors, such as age groups, BMI and number of household members, and underlying diseases, on SARS-CoV-2 infection and to compare the effect of vaccines on the infection occurrence. The linear regression method was used to analyse the effect of vaccines on the level of antibody-induced after each shot of vaccination.

Results

Overall, 962 HCWs including 663 females and 299 males were enrolled in the study. The demographic characteristics of the study population are summarised in Table 1. In all hospitals, most personnel were within the two ends of the age spectrum (very young, <25 years, or middle-aged, >45 years) and mostly had up to three family members. According to reported job titles, based on the available records of the participants, 51 physicians, 96 nurses and 31 laboratory staff were included and 307 HCWs were reported working in other entities. Regarding the ward of activity, only 32 individuals worked in the COVID-19 ward, while others reported working in NICU (n = 52), PICU (n = 41), surgery (n = 77) and other units (n = 760). Thirty-three HCWs (4%) had a positive history of COVID-19 infection before receiving a vaccination. Moreover, a history of close contact with COVID-19 patients was recorded in 42.5% of HCWs (349/820). The vaccine type distribution among HCWs was as follows: 461 Sputnik, 99 Sinopharm, 83 AstraZeneca and 40 other less common vaccinations. Our results showed post-vaccination infection in 3.7% and 5.9% of the individuals after the first and second doses of vaccines, respectively. HCWs with positive serology for COVID-19 compared with negative ones reported more frequently COVID-19 symptoms, including fever (32.9% vs. 18.6%), myalgia (32.6% vs. 17.4%), chills (17% vs. 10.5%), anosmia (17% vs. 10.2%), and headache (26% vs. 17.4%). In the same order, the infected HCWs recorded underlying conditions in higher frequency, including diabetes mellitus (66.6% vs. 33.3%), hypertension (55.5% vs. 44.4%) and cardiovascular disorders (53.3% vs. 46.6%), compared with the non-infected personnel (Table 2).

Table 1. Correlation of SARS-CoV-2 infection with vaccination, gender, job and history of the infection among HCWs

Significant p values are shown in bold.

Table 2. Demographic data related to the participated HCP in this study

As demonstrated in Table 3, the highest levels of anti-spike antibody ratio 3 weeks or more after first and second doses of vaccines were observed among those receiving AstraZeneca (14 ± 91) and Sputnik (14.5 ± 112). Similarly, vaccine-related side effects were more frequent among AstraZeneca recipients after the first dose and among Sputnik recipients after the second dose (mainly in the form of myalgia/arthralgia (72.7% and 86.6%, respectively). After vaccination, only 21 HCWs required hospitalisation and 10 HCWs received COVID-19 medications.

Table 3. Comparison of COVID-19 vaccines in induction of IgG antibody against SARS-CoV-2 spike protein and their side effects in HCWs

Significant p values are shown in bold.

In this study, the higher pre-vaccination antibody was correlated with a lower risk of COVID-19 infection after the first vaccination (P value: 0.014, odds ratio (OR): 0.68) (Table 4). Furthermore, pre-vaccination antibody level was significantly correlated with lower COVID-19 infection after the second dose of vaccine (P value: 0.017, OR: 0.68) (Table 5), meaning that a higher level of antibodies before the first dose of vaccination would decrease the risk of COVID-19 infection after the second dose.

Table 4. Multivariate logistic regression analysis for study of the relationship between different independent variables and the occurrence of SARS-CoV-2 infection after administration of the first vaccine dose in HCWs

Significant p values are shown in bold.

Table 5. Multivariate logistic regression analysis for study of the relationship between different independent variables and the occurrence of SARS-CoV-2 infection after administration of the second vaccine dose in HCWs

Significant p values are shown in bold.

The risk of COVID-19 infection in HCWs receiving AstraZeneca after the first (P value: 0.574, OR: 0.72) and second doses (P value: 0.659, OR: 0.77) was lower than Sputnik; however, it was not statistically significant. In addition, individuals who underwent Sinopharm dose 1 had lower rates of COVID-19 infection (P value: 0.623, OR: 0.57) compared to Sputnik. Nevertheless, this rate was equal among individuals receiving a second dose of Sinopharm and Sputnik (OR: 1) (Supplementary material).

Overall, serum levels of antibodies after the first dose of vaccination were correlated with the forward COVID-19 symptom onset. Results of the linear regression test revealed that the level of antibodies before (P value: 0.064) and after (P value: 0.034) the first dose of vaccination can affect the risk of COVID-19 infection after the first and second vaccines (Supplementary material).

In our study, the association between several factors with antibody levels after the first and second vaccines was also assessed. Serum levels of antibodies before the first dose of vaccine affected antibody levels after receiving the first dose, although it was not statistically significant (P value: 0.089, coefficient: 5.7). Moreover, when compared to AstraZeneca, Sputnik and Sinopharm produced a lower mean of antibody levels, i.e. 12- (P value: 0.186) and 15- (P value: 0.430) fold, respectively. BMI was weakly associated with serum antibody level after the second dose of vaccination. Accordingly, HCWs with higher BMI who had a history of pre-vaccination infection mounted higher levels of antibody after the second dose of vaccination (P value = 0.054, correlation coefficient: 0.13). No association was observed between the level of pre-vaccination antibody and BMI (P value = 0.244) (Supplementary material).

The duration from vaccination to COVID-19 onset in HCWs who were vaccinated with AstraZeneca was longer than that in individuals receiving Sputnik vaccine (P value < 0.001), which could be due to diversity in time points of their introduction for HCP (Supplementary material).

Discussion

In this study, we measured antibodies to SARS-CoV-2 spike protein in HCWs of three Iranian major hospitals to detect adaptive immune response to vaccinations with two doses of either AstraZeneca, Sinopharm or Sputnik. Most HCWs were female and within the two ends of the age spectrum. No correlation was observed between age or gender and COVID-19 seropositivity; however, a relative positive correlation was detected between higher BMI values and serum antibody level after the second dose of vaccination. In a study on 88 Thai HCWs between March and May 2021, seroconversion of anti-spike antibodies 4 weeks after the second dose of the CoronaVac vaccine was observed in almost all HCWs (98.9%). In this study, the anti-spike IgG level was positively correlated with female gender, lower age and normal-weighting [Reference Ongkittikul and Rompho9]. An Irish study on 5788 HCWs showed that seropositivity is higher among healthcare assistants, nurses, individuals with daily exposure to patients with COVID-19, age 18–29 years and living with other HCWs with Asian background, and male sex [Reference Allen10].

Another study measured the antibodies produced against the receptor-binding domain (RBD) of spike-protein and nucleocapsid protein in 314 Turkish HCWs who received the CoronaVac vaccine. Seropositivity was developed in 99.6% of participants 4 weeks after the second dose of the vaccine. It was also shown that individuals who were smokers and/or obese produced lower titres of RBD antibody [Reference Uysal11]. A Greek study evaluated the antibody response of 564 HCWs after two-dose vaccination with BNT162b2 (Comirnaty®; BioNTech and Pfizer) mRNA COVID-19 vaccine. Similar to the Thai study, a greater antibody increase was observed in female and younger age groups [Reference Kontou12]. Contrarily to our finding, other studies found no statistically significant difference in the vaccine antibody levels regarding the BMI in HCWs [Reference Tekol13, Reference Herzberg14].

In the present study, HCWs with pre-vaccination-positive IgG were found to have higher rates of underlying comorbidities, including diabetes mellitus, hypertension and cardiovascular disorders, however, pregnant HCWs were less commonly categorised as IgG-positive group which may pertain to more protection measurement applied before vaccination. We did not assess the correlation between underlying disorders and the level of antibody production. However, a study examined anti-spike antibodies in 515 Indian HCWs in response to AstraZeneca (ChAdOx1-nCOV, Covishield™) and BBV-152 (Covaxin™) vaccines, 21 days or more after taking the first and second doses of both vaccines. In this study less anti-spike antibody was produced in HCWs with age >60 years, male gender, those with any comorbidities and hypertension history. The authors reported a significantly higher seropositivity rate and geometric mean titre for AstraZeneca compared with Covaxin™.

We found vaccine-related side effects more frequently among AstraZeneca recipients after the first dose and among Sputnik recipients after the second dose, mainly with myalgia/arthralgia presentations. Sputnik was the first vaccine used for the vaccination of most Iranian HCWs and some studies have investigated its side effects among HCWs. In a large Iranian study about the side effect of Sputnik among 13 435 HCWs vaccinated between February and April 2021, 3236 self-declaration reports of adverse effects were reported with a higher frequency among female and young participants. Pain at the injection site, fatigue and body pain were reported in almost half of the individuals, followed by headache, fever, joint pain, chilling and drowsiness. Moreover, a detectable level of RBD and neutralising antibodies were found in more than 90% of 238 participants after the first and second doses of vaccine [Reference Babamahmoodi15].

In the current study, we found lower antibody levels in HCWs receiving Sputnik and Sinopharm compared with AstraZeneca. Although this finding could not directly support efficacy of AstraZeneca in HCWs, the efficacy of this vaccine was confirmed by earlier studies. In a small study in Sudan in June 2021, 30 out of 40 (75%) individuals were seropositive for anti-spike IgG after the first dose of the Oxford-AstraZenka vaccine. The antibody titre ranged from 1.2 to 2.7 S/CO (sample mean chemiluminescent signals (RLUs)/cut-off RLUs), with a significantly higher mean titre for females. Side effects similar to our study, including arm pain at the site of the injection, headache, fever, fatigue and gastrointestinal tract disturbances were recorded [Reference Abdaltam, Hammad and Mohamedahmed16].

In our study, the highest levels of anti-spike antibody were measured among HCWs who received AstraZeneca and Sputnik in comparison with Sinopharm, both after the first and second doses of the vaccines. The induced antibody level was significantly increased after the second dose in comparison with the first dose. Consistent with our finding, results of a study on HCWs who received CoronaVac showed a significant increase in anti-spike antibodies after the second dose of vaccination, while an inadequate antibody response was measured after the first dose of the vaccine [Reference Tekol13].

In the current study, HCWs who had a history of pre-vaccination infection mounted higher levels of antibody after the second dose of vaccination. The impact of previous COVID-19 infection on post-vaccination antibody production has been shown in a few studies. Parai et al. [Reference Parai17] evaluated antibodies against anti-spike and nucleocapsid proteins in 134 Indian HCWs before and 28 days after receiving two dosages of either BBV-152 or AZD1222 vaccines from January 2021 to April 2021. After a single dose, 96% of HCWs with prior COVID-19 infection were found to be seropositive, while only 61.3% of non-infected HCWs developed antibodies, which increased to 82.7% after the second dose [Reference Parai17]. In the Kontou survey [Reference Kontou12], HCWs with a positive history of natural COVID-19 and/or those working in COVID-19 clinics produced higher titres of antibody after the first dose. Another study in Israel investigated BNT162b2 mRNA COVID-19 vaccine immunogenicity 21 days after the first dose in 514 HCWs. Similar to other studies, immunogenicity decreased with age. Notably, antibody titres in those with prior infection were higher than naïve individuals regardless of the presence of detectable pre-vaccination IgG antibodies [Reference Abu Jabal18]. In a study from Turkey, 1072 HCWs were evaluated after 28 days of the first, and 21 days of the second dose of CoronaVac. After the first and second doses, anti-spike antibodies were detected in 834 (77.8%) and 1008 (99.6%) HCWs, respectively. Seropositivity was considerably higher among females and was found to be highest in participants aged 18–34 years. Antibody titres were significantly higher in those who had COVID-19 infection before vaccination and lower in HCWs with chronic diseases [Reference Bayram19]. In a recent study that was performed on 59 HCWs residing in Maryland and receiving Pfizer-BioNTech or Moderna vaccine, participants with previous COVID-19 infection had higher antibody titre in response to a single dose of mRNA vaccine than those who were not previously infected. Furthermore, antibodies achieved higher titres and neutralisation compared with Ab-negative volunteers [Reference Saadat20]. Urbanowicz et al. followed 45 HCWs serologically and repeated SARS-CoV-2 antigenic exposure, through vaccination or natural infection, and their results showed that multiple exposures to SARS-CoV-2 spike protein could expand reactive spike-specific antibody responses [Reference Urbanowicz21].

Our results showed post-vaccination infection in 3.7% and 5.9% of the individuals after the first and second doses of vaccines, respectively. The infection was significantly lower in HCWs who presented higher antibody titres before the vaccination. The results also showed low frequency of hospitalisation among the partially and fully vaccinated HCWs. In a case series study in Saudi Arabia, 20 HCWs who experienced the new infection after receiving the Pfizer-BioNTech COVID-19 vaccine were analysed. Most of the HCWs in this study had COVID-19 infection within the first and the second weeks of vaccination, and infection after the third week decreased, as confirmed infection after the second dose of vaccine was reported only in two HCWs [Reference Alshamrani22]. In a study in India, post-vaccination infection with SARS-CoV-2 was recorded in 2.63% of vaccinated HCWs with AstraZeneca (76.5% and 23.5% of these cases were among the fully vaccinated and partially vaccinated HCWs, respectively). The infection similarly caused a reduced rate of hospitalisation in these HCWs (0.06%) [Reference Vaishya23].

This study had several limitations. We performed blood sampling at different time points which may affect longitudinal correlation in terms of vaccine-related seropositivity. Furthermore, we could not evaluate vaccine efficacy among participants as all personnel had already received vaccination and we could not make a comparison between HCWs with and without vaccinations. However, this study represents the first study reporting vaccine outcome among HCWs from a developing health setting. Further studies with more sample size on individuals other than HCWs are required to characterise variable aspects of vaccine administration, and besides humoral immunity, molecular studies investigating probable cellular immunity mechanisms are needed.

In conclusion, our results showed a diversity among different brands of COVID-19 vaccines regarding the induced antibody levels and side effects; however, it seems that two doses of the vaccines could induce antibody response in the most of HCWs. History of previous infection with SARS-CoV-2 seems to boost stronger humoral immunity in HCWs, regardless of types of the vaccines. Our findings showed increase in the number of infection after 3–5 months of the second vaccination course. Further follow-up study is needed to show protection of the vaccines against common variants of SARS-CoV-2 circulating among children and HCWs who are in their contact.

Supplementary material

The supplementary material for this article can be found at https://doi.org/10.1017/S0950268822001984.

Acknowledgements

The authors would like to thank all staff of Mofid Children's Hospital, Nikan hospital and counsellors in Clinical Research Development Center of Children Hospital, Hormozgan University of Medical Sciences, Bandar Abbas, Iran for their help.

Financial support

This study was supported by Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran (Grant numbers 29578 and 27744), Deputy of Research Affairs, Shahid Beheshti University of Medical Sciences, Tehran, Iran, and the Robert Koch Institute (Germany) that supported this study by providing diagnostic material through a special COVID pandemic grant from the German Ministry of Health.

Conflict of interest

None.

Data availability statement

Anonymous data are available upon reasonable request to the corresponding author.

Footnotes

*

These authors contributed equally to this study.

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Figure 0

Table 1. Correlation of SARS-CoV-2 infection with vaccination, gender, job and history of the infection among HCWs

Figure 1

Table 2. Demographic data related to the participated HCP in this study

Figure 2

Table 3. Comparison of COVID-19 vaccines in induction of IgG antibody against SARS-CoV-2 spike protein and their side effects in HCWs

Figure 3

Table 4. Multivariate logistic regression analysis for study of the relationship between different independent variables and the occurrence of SARS-CoV-2 infection after administration of the first vaccine dose in HCWs

Figure 4

Table 5. Multivariate logistic regression analysis for study of the relationship between different independent variables and the occurrence of SARS-CoV-2 infection after administration of the second vaccine dose in HCWs

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