Comparison of antibody response durability of mRNA-1273, BNT162b2, and Ad26.COV2.S SARS-CoV-2 vaccines in healthcare workers
- PMID: 36044963
- PMCID: PMC9420538
- DOI: 10.1016/j.ijid.2022.08.022
Comparison of antibody response durability of mRNA-1273, BNT162b2, and Ad26.COV2.S SARS-CoV-2 vaccines in healthcare workers
Abstract
Objectives: There are limited comparative immunologic durability data post COVID-19 vaccinations.
Methods: Approximately 8.4 months after primary COVID-19 vaccination, 647 healthcare workers completed surveys about COVID-19 vaccinations/infections and blood draws. The groups included participants vaccinated with mRNA-1273 (n = 387), BNT162b2 (n = 212), or Ad26.COV2.S (n = 10) vaccines; unvaccinated participants (n = 10); and participants who received a booster dose (n = 28). The primary outcome was immunoglobin anti-spike titer. Secondary/tertiary outcomes included neutralizing antibodies (enzyme-linked immunosorbent assay-based pseudoneutralization) and vaccine effectiveness (VE). Antibody levels were compared using analysis of variance and linear regression.
Results: Mean age was 49.7 and 75.3% of the participants were female. Baseline variables were balanced except for immunosuppression, previous COVID-19 infection, and post-primary vaccination time. Unadjusted median (interquartile range [IQR]) anti-spike titers (AU/ml) were 1539.5 (876.7-2626.7) for mRNA-1273, 751.2 (422.0-1381.5) for BNT162b2, 451.6 (103.0-2396.7) for Ad26.COV2.S, 113.4 (3.7-194.0) for unvaccinated participants, and 31898.8 (21347.1-45820.1) for participants administered with booster dose (mRNA-1273 vs BNT162b2, P <.001; mRNA-1273, BNT162b2, or boosted vs unvaccinated, P <.006; mRNA-1273, BNT162b2, Ad26.COV2.S, or unvaccinated vs boosted, P <.001). Unadjusted median (IQR) pseudoneutralization was as follows: 90.9% (80.1-95.0) for mRNA-1273, 77.2% (59.1-89.9) for BNT162b2, 57.9% (36.6-95.8) for Ad26.COV2.S, 40.1% (21.7-60.6) for unvaccinated, and 96.4% (96.1-96.6) for participants administered with booster dose (mRNA-1273 vs BNT162b2, P <.001; mRNA-1273, BNT162b2, or boosted vs unvaccinated, P <.028; mRNA-1273, BNT162b2, Ad26.COV2.S, or unvaccinated vs boosted, P <.001). VE was 87-89% for participants administered mRNA-1273 vaccine, BNT162b2 vaccine, and booster dose, and 33% for Ad26.COV2.S (none significantly different).
Conclusion: Antibody responses 8.4 months after primary vaccination were significantly higher with mRNA-1273 than those observed with BNT162b2.
Keywords: Anti-spike antibody; Antibody responses; COVID-19; SARS-CoV-2; Vaccine effectiveness.
Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.
Conflict of interest statement
Conflict of interest The authors have no competing interests to declare.
Figures

Similar articles
-
Humoral and cellular immunogenicity of homologous and heterologous booster vaccination in Ad26.COV2.S-primed individuals: Comparison by breakthrough infection.Front Immunol. 2023 Mar 7;14:1131229. doi: 10.3389/fimmu.2023.1131229. eCollection 2023. Front Immunol. 2023. PMID: 36960070 Free PMC article.
-
Immunogenicity and Reactogenicity of Vaccine Boosters after Ad26.COV2.S Priming.N Engl J Med. 2022 Mar 10;386(10):951-963. doi: 10.1056/NEJMoa2116747. Epub 2022 Jan 19. N Engl J Med. 2022. PMID: 35045226 Free PMC article. Clinical Trial.
-
Durability of Heterologous and Homologous COVID-19 Vaccine Boosts.JAMA Netw Open. 2022 Aug 1;5(8):e2226335. doi: 10.1001/jamanetworkopen.2022.26335. JAMA Netw Open. 2022. PMID: 35947380 Free PMC article.
-
Immunogenicity and efficacy of Ad26.COV2.S: An adenoviral vector-based COVID-19 vaccine.Immunol Rev. 2022 Sep;310(1):47-60. doi: 10.1111/imr.13088. Epub 2022 Jun 11. Immunol Rev. 2022. PMID: 35689434 Free PMC article. Review.
-
Longevity of immunity following COVID-19 vaccination: a comprehensive review of the currently approved vaccines.Hum Vaccin Immunother. 2022 Nov 30;18(5):2037384. doi: 10.1080/21645515.2022.2037384. Epub 2022 Apr 13. Hum Vaccin Immunother. 2022. PMID: 35417285 Free PMC article. Review.
Cited by
-
Predictors of long-term neutralizing antibody titers following COVID-19 vaccination by three vaccine types: the BOOST study.Sci Rep. 2023 May 9;13(1):6505. doi: 10.1038/s41598-023-33320-x. Sci Rep. 2023. PMID: 37160978 Free PMC article.
-
Exposure of progressive immune dysfunction by SARS-CoV-2 mRNA vaccination in patients with chronic lymphocytic leukemia: A prospective cohort study.PLoS Med. 2023 Jun 29;20(6):e1004157. doi: 10.1371/journal.pmed.1004157. eCollection 2023 Jun. PLoS Med. 2023. PMID: 37384638 Free PMC article.
-
Revealing the significance of IL-2 and IL-5 in SARS-CoV-2-specific T-cell responses in kidney transplant recipients.Npj Viruses. 2024 Feb 14;2(1):7. doi: 10.1038/s44298-024-00015-7. Npj Viruses. 2024. PMID: 40295737 Free PMC article.
-
The Equal Neutralizing Effectiveness of BNT162b2, ChAdOx1 nCoV-19, and Sputnik V Vaccines in the Palestinian Population.Vaccines (Basel). 2024 May 3;12(5):493. doi: 10.3390/vaccines12050493. Vaccines (Basel). 2024. PMID: 38793744 Free PMC article.
-
Effectiveness of Pfizer Vaccine BNT162b2 Against SARS-CoV-2 in Americans 16 and Older: A Systematic Review.Cureus. 2024 Jul 22;16(7):e65111. doi: 10.7759/cureus.65111. eCollection 2024 Jul. Cureus. 2024. PMID: 39171051 Free PMC article. Review.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous