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Comparative Magnitude and Persistence of Humoral SARS-CoV-2 Vaccination Responses in the Adult Population in Germany.

Authors :
Dulovic A
Kessel B
Harries M
Becker M
Ortmann J
Griesbaum J
Jüngling J
Junker D
Hernandez P
Gornyk D
Glöckner S
Melhorn V
Castell S
Heise JK
Kemmling Y
Tonn T
Frank K
Illig T
Klopp N
Warikoo N
Rath A
Suckel C
Marzian AU
Grupe N
Kaiser PD
Traenkle B
Rothbauer U
Kerrinnes T
Krause G
Lange B
Schneiderhan-Marra N
Strengert M
Source :
Frontiers in immunology [Front Immunol] 2022 Feb 16; Vol. 13, pp. 828053. Date of Electronic Publication: 2022 Feb 16 (Print Publication: 2022).
Publication Year :
2022

Abstract

Recent increases in SARS-CoV-2 infections have led to questions about duration and quality of vaccine-induced immune protection. While numerous studies have been published on immune responses triggered by vaccination, these often focus on studying the impact of one or two immunisation schemes within subpopulations such as immunocompromised individuals or healthcare workers. To provide information on the duration and quality of vaccine-induced immune responses against SARS-CoV-2, we analyzed antibody titres against various SARS-CoV-2 antigens and ACE2 binding inhibition against SARS-CoV-2 wild-type and variants of concern in samples from a large German population-based seroprevalence study (MuSPAD) who had received all currently available immunisation schemes. We found that homologous mRNA-based or heterologous prime-boost vaccination produced significantly higher antibody responses than vector-based homologous vaccination. Ad26.CoV2S.2 performance was particularly concerning with reduced titres and 91.7% of samples classified as non-responsive for ACE2 binding inhibition, suggesting that recipients require a booster mRNA vaccination. While mRNA vaccination induced a higher ratio of RBD- and S1-targeting antibodies, vector-based vaccines resulted in an increased proportion of S2-targeting antibodies. Given the role of RBD- and S1-specific antibodies in neutralizing SARS-CoV-2, their relative over-representation after mRNA vaccination may explain why these vaccines have increased efficacy compared to vector-based formulations. Previously infected individuals had a robust immune response once vaccinated, regardless of which vaccine they received, which could aid future dose allocation should shortages arise for certain manufacturers. Overall, both titres and ACE2 binding inhibition peaked approximately 28 days post-second vaccination and then decreased.<br />Competing Interests: NS-M was a speaker at Luminex user meetings in the past. The Natural and Medical Sciences Institute at the University of Tübingen is involved in applied research projects as a fee for services with the Luminex Corporation. 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 Dulovic, Kessel, Harries, Becker, Ortmann, Griesbaum, Jüngling, Junker, Hernandez, Gornyk, Glöckner, Melhorn, Castell, Heise, Kemmling, Tonn, Frank, Illig, Klopp, Warikoo, Rath, Suckel, Marzian, Grupe, Kaiser, Traenkle, Rothbauer, Kerrinnes, Krause, Lange, Schneiderhan-Marra and Strengert.)

Details

Language :
English
ISSN :
1664-3224
Volume :
13
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
35251012
Full Text :
https://doi.org/10.3389/fimmu.2022.828053