Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Dec 26;11(1):56.
doi: 10.3390/vaccines11010056.

Immunogenicity of BNT162b2, BBIBP-CorV, Gam-COVID-Vac and ChAdOx1 nCoV-19 Vaccines Six Months after the Second Dose: A Longitudinal Prospective Study

Affiliations

Immunogenicity of BNT162b2, BBIBP-CorV, Gam-COVID-Vac and ChAdOx1 nCoV-19 Vaccines Six Months after the Second Dose: A Longitudinal Prospective Study

Vladimir Petrović et al. Vaccines (Basel). .

Abstract

Many available SARS-CoV-2 vaccines demonstrated good humoral response, but studies directly comparing their immunogenicity in the general population are lacking. We evaluated the medium−term kinetics of anti-S SARS-CoV-2 antibodies (Abs) at one and six months after the second dose of BNT162b2, BBIBP-CorV, and Gam-COVID-Vac. Immunogenicity at six months was directly compared between BNT162b2, BBIBP-CorV, Gam-COVID-Vac, and ChAdOx1 nCoV-19. Participants ≥ 20 years old from Novi Sad, Serbia, without prior SARS-CoV-2 infection, were included. Anti S1/S2 IgG antibodies were measured using quantitative LIAISON SARS-CoV-2 assay. A total of 368 participants were included: 231 (62.77%) had sera collected at two time points. Two doses of BNT162b2 were received by 37.50% of participants, followed by BBIBP-CorV (22.01%), Gam-COVID-Vac (21.47%), and ChAdOx1 nCoV-19 (19.02%). Mean Ab levels at the 28th day and 6 months were 216.55 (SD = 105.73) AU/mL and 75.68 (SD = 57.30) for BNT162b2, 194.38 (SD = 140.24) and 90.53 (SD = 111.30) for Gam-COVID-Vac, and 72.74 (SD = 80.04) and 24.43 (SD = 38.43) for BBIBP-CorV group (p < 0.01, between two time points across all three groups), with a significant difference between women and men (p < 0.01, for both sexes). At the sixth month post-vaccination, the highest mean Ab level was detected in Gam-COVID-Vac group (91.28 AU/mL, SD = 95.96), followed by BNT162b2 (85.25 AU/mL, SD = 60.02), ChAdOx1 nCoV-19 (64.22 AU/mL, SD = 65.30), and BBIBP-CorV (25.26 AU/mL, SD = 36.92) (p < 0.01). Anti-spike IgG persistence was demonstrated six months post-vaccination with a significant decline in Ab levels. These results suggest a lower protection against SARS-CoV-2 over time. Our findings support the introduction of additional (booster) doses.

Keywords: BBIBP-CorV; BNT162b2; COVID-19; ChAdOx1 nCoV-19; Gam-COVID-Vac; immunogenicity; vaccine.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 3
Figure 3
Correlation between Ab levels at the 28th day and 6 months after the second dose of BNT162b2 (A), BBIBP-CorV (B) and Gam-COVID-Vac (C). rho = Spearman’s correlation coefficient.
Figure 1
Figure 1
Distribution of participants, stratified by vaccine type, sex and number (single or paired) of samples.
Figure 2
Figure 2
Antibody levels at the 28th day and 6 months after the second dose of vaccine, stratified by sex (A) and age groups (B) of participants. Legend: *** p < 0.001, ** p < 0.01, * p < 0.05, ns = not significant, NA = not applicable.
Figure 4
Figure 4
Antibody levels at 6 months after the administration of BNT162b2, BBIBP-CorV, Gam-COVID-Vac and ChAdOx1 nCoV-19 vaccines, stratified by sex (A) and age groups (B) of participants. Legend: *** p < 0.001, ** p < 0.01, * p < 0.05, ns = not significant.

Similar articles

Cited by

References

    1. Pollard C.A., Morran M.P., Nestor-Kalinoski A.L. The COVID-19 pandemic: A global health crisis. Physiol. Genomics. 2020;52:549–557. doi: 10.1152/physiolgenomics.00089.2020. - DOI - PMC - PubMed
    1. Gebru A.A., Birhanu T., Wendimu E., Ayalew A.F., Mulat S., Abasimel H.Z., Kazemi A., Tadesse B.A., Gebru B.A., Deriba B.S., et al. Global burden of COVID-19: Situational analyis and review. Hum. Antibodies. 2021;29:139–148. doi: 10.3233/HAB-200420. - DOI - PubMed
    1. Jeyanathan M., Afkhami S., Smaill F., Miller M.S., Lichty B.D., Xing Z. Immunological considerations for COVID-19 vaccine strategies. Nat. Rev. Immunol. 2020;20:615–632. doi: 10.1038/s41577-020-00434-6. - DOI - PMC - PubMed
    1. Papadopoli R., De Sarro C., Palleria C., Gallelli L., Pileggi C., De Sarro G. Serological Response to SARS-CoV-2 Messenger RNA Vaccine: Real-World Evidence from Italian Adult Population. Vaccines. 2021;9:1494. doi: 10.3390/vaccines9121494. - DOI - PMC - PubMed
    1. Creech C.B., Walker S.C., Samuels R.J. SARS-CoV-2 Vaccines. JAMA. 2021;325:1318. doi: 10.1001/jama.2021.3199. - DOI - PubMed

LinkOut - more resources