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Trajectory of IgG to SARS-CoV-2 After Vaccination With BNT162b2 or mRNA-1273 in an Employee Cohort and Comparison With Natural Infection.

Authors :
Keshavarz B
Richards NE
Workman LJ
Patel J
Muehling LM
Canderan G
Murphy DD
Brovero SG
Ailsworth SM
Eschenbacher WH
McGowan EC
Mann BJ
Nelson MR
Kadl A
Woodfolk JA
Platts-Mills TAE
Wilson JM
Source :
Frontiers in immunology [Front Immunol] 2022 Mar 21; Vol. 13, pp. 850987. Date of Electronic Publication: 2022 Mar 21 (Print Publication: 2022).
Publication Year :
2022

Abstract

Three COVID-19 vaccines have received FDA-authorization and are in use in the United States, but there is limited head-to-head data on the durability of the immune response elicited by these vaccines. Using a quantitative assay we studied binding IgG antibodies elicited by BNT162b2, mRNA-1273 or Ad26.COV2.S in an employee cohort over a span out to 10 months. Age and sex were explored as response modifiers. Of 234 subjects in the vaccine cohort, 114 received BNT162b2, 114 received mRNA-1273 and six received Ad26.COV2.S. IgG levels measured between seven to 20 days after the second vaccination were similar in recipients of BNT162b2 and mRNA-127 and were ~50-fold higher than in recipients of Ad26.COV2.S. However, by day 21 and at later time points IgG levels elicited by BNT162b2 were lower than mRNA-1273. Accordingly, the IgG decay curve was steeper for BNT162b2 than mRNA-1273. Age was a significant modifier of IgG levels in recipients of BNT162b2, but not mRNA-1273. After six months, IgG levels elicited by BNT162b2, but not mRNA-1273, were lower than IgG levels in patients who had been hospitalized with COVID-19 six months earlier. Similar findings were observed when comparing vaccine-elicited antibodies with steady-state IgG targeting seasonal human coronaviruses. Differential IgG decay could contribute to differences observed in clinical protection over time between BNT162b2 and mRNA-1273.<br />Competing Interests: TP-M and JMW have received assay support from Thermo-Fisher/Phadia, but not for work related to this project. JMW has received consultancy fees from Thermo-Fisher/Phadia for work unrelated to this project. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2022 Keshavarz, Richards, Workman, Patel, Muehling, Canderan, Murphy, Brovero, Ailsworth, Eschenbacher, McGowan, Mann, Nelson, Kadl, Woodfolk, Platts-Mills and Wilson.)

Details

Language :
English
ISSN :
1664-3224
Volume :
13
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
35386716
Full Text :
https://doi.org/10.3389/fimmu.2022.850987