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High baseline expression of IL-6 and IL-10 decreased CCR7 B cells in individuals with previous SARS-CoV-2 infection during BNT162b2 vaccination

Authors :
Alberto Ponciano-Gómez
Martha Iris Valle-Solis
Myriam Campos-Aguilar
Rafael Jijón-Lorenzo
Elena de la C. Herrera-Cogco
Roberto Ramos-Alor
César Isaac Bazán-Mendez
Gustavo Antonio Pérez-Gil Cervantes
Ricardo Ávila-García
Abdiel González Aguilar
Moises Geovani Salmerón Texale
Wilfrido David Tapia-Sánchez
Carlos Leonardo Duarte-Martínez
Sandra Olivas-Quintero
Santiago Cristobal Sigrist-Flores
Itzell Alejandrina Gallardo-Ortíz
Rafael Villalobos-Molina
Adolfo Rene Méndez-Cruz
Rafael Jimenez-Flores
Leopoldo Santos-Argumedo
Juan Pedro Luna-Arias
Hector Romero-Ramírez
Victor Hugo Rosales-García
Bartolo Avendaño-Borromeo
Source :
Frontiers in Immunology, Vol 13 (2022)
Publication Year :
2022
Publisher :
Frontiers Media S.A., 2022.

Abstract

The current pandemic generated by SARS-CoV-2 has led to mass vaccination with different biologics that have shown wide variations among human populations according to the origin and formulation of the vaccine. Studies evaluating the response in individuals with a natural infection before vaccination have been limited to antibody titer analysis and evaluating a few humoral and cellular response markers, showing a more rapid and intense humoral response than individuals without prior infection. However, the basis of these differences has not been explored in depth. In the present work, we analyzed a group of pro and anti-inflammatory cytokines, antibody titers, and cell populations in peripheral blood of individuals with previous SARS-CoV-2 infection using BNT162b2 biologic. Our results suggest that higher antibody concentration in individuals with an earlier disease could be generated by higher production of plasma cells to the detriment of the presence of memory B cells in the bloodstream, which could be related to the high baseline expression of cytokines (IL-6 and IL-10) before vaccination.

Details

Language :
English
ISSN :
16643224
Volume :
13
Database :
Directory of Open Access Journals
Journal :
Frontiers in Immunology
Publication Type :
Academic Journal
Accession number :
edsdoj.9de834a23e8b470ebe5dd071217e9be3
Document Type :
article
Full Text :
https://doi.org/10.3389/fimmu.2022.946770