SARS-CoV-2 IgG Spike antibody levels and avidity in natural infection or following vaccination with mRNA-1273 or BNT162b2 vaccines

Certain aspects of the immunogenicity and effectiveness of the messenger ribonucleic acid (mRNA) vaccines (mRNA-1273 and BNT162b2) developed in response to the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic are still uncharacterized. Serum or plasma samples from healthy donor...

Full description

Bibliographic Details
Main Authors: Thomas E. Hickey, Troy J. Kemp, Jimmie Bullock, Aaron Bouk, Jordan Metz, Abigail Neish, James Cherry, Douglas R. Lowy, Ligia A. Pinto
Format: Article
Language:English
Published: Taylor & Francis Group 2023-08-01
Series:Human Vaccines & Immunotherapeutics
Subjects:
Online Access:http://dx.doi.org/10.1080/21645515.2023.2215677
_version_ 1797673022590550016
author Thomas E. Hickey
Troy J. Kemp
Jimmie Bullock
Aaron Bouk
Jordan Metz
Abigail Neish
James Cherry
Douglas R. Lowy
Ligia A. Pinto
author_facet Thomas E. Hickey
Troy J. Kemp
Jimmie Bullock
Aaron Bouk
Jordan Metz
Abigail Neish
James Cherry
Douglas R. Lowy
Ligia A. Pinto
author_sort Thomas E. Hickey
collection DOAJ
description Certain aspects of the immunogenicity and effectiveness of the messenger ribonucleic acid (mRNA) vaccines (mRNA-1273 and BNT162b2) developed in response to the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic are still uncharacterized. Serum or plasma samples from healthy donor recipients of either vaccine (BNT162b2 n = 53, mRNA-1273 n = 49; age 23–67), and individuals naturally infected with SARS-CoV-2 (n = 106; age 18–82) were collected 0–2 months post-infection or 1- and 4 months after second dose of vaccination. Anti-Spike antibody levels and avidity were measured via an enzyme-linked immunosorbent assay (ELISA). Overall, vaccination induced higher circulating anti-Spike protein immunoglobulin G (IgG) antibody levels and avidity compared to infection at similar time intervals. Both vaccines produced similar anti-Spike IgG concentrations at 1 month, while mRNA-1273 demonstrated significantly higher circulating antibody concentrations after 4 months. mRNA-1273 induced significantly higher avidity at month 1 compared to BNT162b2 across all age groups. However, the 23–34 age group was the only group to maintain statistical significance by 4 months. Male BNT162b2 recipients were approaching statistically significant lower anti-Spike IgG avidity compared to females by month 4. These findings demonstrate enhanced anti-Spike IgG levels and avidity following vaccination compared to natural infection. In addition, the mRNA-1273 vaccine induced higher antibody levels by 4 months compared to BNT162b2.
first_indexed 2024-03-11T21:39:24Z
format Article
id doaj.art-0a66c134f1764754ac6c6d4cd549e4a5
institution Directory Open Access Journal
issn 2164-5515
2164-554X
language English
last_indexed 2024-03-11T21:39:24Z
publishDate 2023-08-01
publisher Taylor & Francis Group
record_format Article
series Human Vaccines & Immunotherapeutics
spelling doaj.art-0a66c134f1764754ac6c6d4cd549e4a52023-09-26T13:25:50ZengTaylor & Francis GroupHuman Vaccines & Immunotherapeutics2164-55152164-554X2023-08-0119210.1080/21645515.2023.22156772215677SARS-CoV-2 IgG Spike antibody levels and avidity in natural infection or following vaccination with mRNA-1273 or BNT162b2 vaccinesThomas E. Hickey0Troy J. Kemp1Jimmie Bullock2Aaron Bouk3Jordan Metz4Abigail Neish5James Cherry6Douglas R. Lowy7Ligia A. Pinto8Frederick National Laboratory for Cancer ResearchFrederick National Laboratory for Cancer ResearchFrederick National Laboratory for Cancer ResearchNational Cancer InstituteFrederick National Laboratory for Cancer ResearchFrederick National Laboratory for Cancer ResearchNational Institutes of HealthNational Institutes of HealthFrederick National Laboratory for Cancer ResearchCertain aspects of the immunogenicity and effectiveness of the messenger ribonucleic acid (mRNA) vaccines (mRNA-1273 and BNT162b2) developed in response to the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic are still uncharacterized. Serum or plasma samples from healthy donor recipients of either vaccine (BNT162b2 n = 53, mRNA-1273 n = 49; age 23–67), and individuals naturally infected with SARS-CoV-2 (n = 106; age 18–82) were collected 0–2 months post-infection or 1- and 4 months after second dose of vaccination. Anti-Spike antibody levels and avidity were measured via an enzyme-linked immunosorbent assay (ELISA). Overall, vaccination induced higher circulating anti-Spike protein immunoglobulin G (IgG) antibody levels and avidity compared to infection at similar time intervals. Both vaccines produced similar anti-Spike IgG concentrations at 1 month, while mRNA-1273 demonstrated significantly higher circulating antibody concentrations after 4 months. mRNA-1273 induced significantly higher avidity at month 1 compared to BNT162b2 across all age groups. However, the 23–34 age group was the only group to maintain statistical significance by 4 months. Male BNT162b2 recipients were approaching statistically significant lower anti-Spike IgG avidity compared to females by month 4. These findings demonstrate enhanced anti-Spike IgG levels and avidity following vaccination compared to natural infection. In addition, the mRNA-1273 vaccine induced higher antibody levels by 4 months compared to BNT162b2.http://dx.doi.org/10.1080/21645515.2023.2215677avidityiggsars-cov-2serologyvaccinesinfectionspike
spellingShingle Thomas E. Hickey
Troy J. Kemp
Jimmie Bullock
Aaron Bouk
Jordan Metz
Abigail Neish
James Cherry
Douglas R. Lowy
Ligia A. Pinto
SARS-CoV-2 IgG Spike antibody levels and avidity in natural infection or following vaccination with mRNA-1273 or BNT162b2 vaccines
Human Vaccines & Immunotherapeutics
avidity
igg
sars-cov-2
serology
vaccines
infection
spike
title SARS-CoV-2 IgG Spike antibody levels and avidity in natural infection or following vaccination with mRNA-1273 or BNT162b2 vaccines
title_full SARS-CoV-2 IgG Spike antibody levels and avidity in natural infection or following vaccination with mRNA-1273 or BNT162b2 vaccines
title_fullStr SARS-CoV-2 IgG Spike antibody levels and avidity in natural infection or following vaccination with mRNA-1273 or BNT162b2 vaccines
title_full_unstemmed SARS-CoV-2 IgG Spike antibody levels and avidity in natural infection or following vaccination with mRNA-1273 or BNT162b2 vaccines
title_short SARS-CoV-2 IgG Spike antibody levels and avidity in natural infection or following vaccination with mRNA-1273 or BNT162b2 vaccines
title_sort sars cov 2 igg spike antibody levels and avidity in natural infection or following vaccination with mrna 1273 or bnt162b2 vaccines
topic avidity
igg
sars-cov-2
serology
vaccines
infection
spike
url http://dx.doi.org/10.1080/21645515.2023.2215677
work_keys_str_mv AT thomasehickey sarscov2iggspikeantibodylevelsandavidityinnaturalinfectionorfollowingvaccinationwithmrna1273orbnt162b2vaccines
AT troyjkemp sarscov2iggspikeantibodylevelsandavidityinnaturalinfectionorfollowingvaccinationwithmrna1273orbnt162b2vaccines
AT jimmiebullock sarscov2iggspikeantibodylevelsandavidityinnaturalinfectionorfollowingvaccinationwithmrna1273orbnt162b2vaccines
AT aaronbouk sarscov2iggspikeantibodylevelsandavidityinnaturalinfectionorfollowingvaccinationwithmrna1273orbnt162b2vaccines
AT jordanmetz sarscov2iggspikeantibodylevelsandavidityinnaturalinfectionorfollowingvaccinationwithmrna1273orbnt162b2vaccines
AT abigailneish sarscov2iggspikeantibodylevelsandavidityinnaturalinfectionorfollowingvaccinationwithmrna1273orbnt162b2vaccines
AT jamescherry sarscov2iggspikeantibodylevelsandavidityinnaturalinfectionorfollowingvaccinationwithmrna1273orbnt162b2vaccines
AT douglasrlowy sarscov2iggspikeantibodylevelsandavidityinnaturalinfectionorfollowingvaccinationwithmrna1273orbnt162b2vaccines
AT ligiaapinto sarscov2iggspikeantibodylevelsandavidityinnaturalinfectionorfollowingvaccinationwithmrna1273orbnt162b2vaccines