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Atypical B cells and impaired SARS-CoV-2 neutralization following heterologous vaccination in the elderly.

Authors :
Ferreira IATM
Lee CYC
Foster WS
Abdullahi A
Dratva LM
Tuong ZK
Stewart BJ
Ferdinand JR
Guillaume SM
Potts MOP
Perera M
Krishna BA
Peñalver A
Cabantous M
Kemp SA
Ceron-Gutierrez L
Ebrahimi S
Lyons P
Smith KGC
Bradley J
Collier DA
McCoy LE
van der Klaauw A
Thaventhiran JED
Farooqi IS
Teichmann SA
MacAry PA
Doffinger R
Wills MR
Linterman MA
Clatworthy MR
Gupta RK
Source :
Cell reports [Cell Rep] 2023 Aug 29; Vol. 42 (8), pp. 112991. Date of Electronic Publication: 2023 Aug 16.
Publication Year :
2023

Abstract

Suboptimal responses to a primary vaccination course have been reported in the elderly, but there is little information regarding the impact of age on responses to booster third doses. Here, we show that individuals 70 years or older (median age 73, range 70-75) who received a primary two-dose schedule with AZD1222 and booster third dose with mRNA vaccine achieve significantly lower neutralizing antibody responses against SARS-CoV-2 spike pseudotyped virus compared with those younger than 70 (median age 66, range 54-69) at 1 month post booster. Impaired neutralization potency and breadth post third dose in the elderly is associated with circulating "atypical" spike-specific B cells expressing CD11c and FCRL5. However, when considering individuals who received three doses of mRNA vaccine, we did not observe differences in neutralization or enrichment in atypical B cells. This work highlights the finding that AdV and mRNA COVID-19 vaccine formats differentially instruct the memory B cell response.<br />Competing Interests: Declaration of interests R.K.G. has received honoraria for consulting and educational activities from Gilead, GSK, Janssen, and Moderna.<br /> (Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
2211-1247
Volume :
42
Issue :
8
Database :
MEDLINE
Journal :
Cell reports
Publication Type :
Academic Journal
Accession number :
37590132
Full Text :
https://doi.org/10.1016/j.celrep.2023.112991