CD4+ T Cell Immune Specificity Changes After Vaccination in Healthy And COVID-19 Convalescent Subjects.
Adult
BNT162 Vaccine
/ immunology
CD4-Positive T-Lymphocytes
/ immunology
COVID-19
/ immunology
Cells, Cultured
Convalescence
Female
Healthy Volunteers
Humans
Immunization, Secondary
Immunoglobulin A
/ metabolism
Immunoglobulin G
/ metabolism
Male
Middle Aged
SARS-CoV-2
/ physiology
Spike Glycoprotein, Coronavirus
/ immunology
T-Cell Antigen Receptor Specificity
Vaccination
COVID-19
T cell
adaptive immunity
immune profile
vaccination
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2021
2021
Historique:
received:
09
08
2021
accepted:
29
12
2021
entrez:
7
2
2022
pubmed:
8
2
2022
medline:
22
2
2022
Statut:
epublish
Résumé
The immune response promoted by SARS-CoV-2 vaccination is relevant to develop novel vaccines and optimized prevention strategies. We analyzed the adaptive immunity in healthy donors (HD) and convalescent individuals (CD), before and after administering BNT162b2 vaccine. Our results revealed specific changes in CD4+ T cell reactivity profile in vaccinated HD and CD, with an increase in S1 and S2 positive individuals, proportionally higher for S2. On the contrary, NCAP reactivity observed in HD and CD patients was no longer detectable after vaccination. Despite the substantial antibody response in CD, MPro-derived peptides did not elicit CD4+ lymphocyte activation in our assay in either condition. HD presented an increment in anti-S and anti-RBD IgG after first dose vaccination, which increased after the second vaccination. Conversely, anti-S and anti-RBD IgG and IgA titers increased in already positive CD after first dose administration, remaining stable after second dose inoculation. Interestingly, we found a strong significant correlation between S1-induced CD4+ response and anti-S IgA pre-vaccination, which was lost after vaccine administration.
Identifiants
pubmed: 35126347
doi: 10.3389/fimmu.2021.755891
pmc: PMC8807633
doi:
Substances chimiques
Immunoglobulin A
0
Immunoglobulin G
0
Spike Glycoprotein, Coronavirus
0
spike protein, SARS-CoV-2
0
BNT162 Vaccine
N38TVC63NU
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
755891Informations de copyright
Copyright © 2022 Esparcia-Pinedo, Martínez-Fleta, Ropero, Vera-Tomé, Reyburn, Casasnovas, Rodríguez Frade, Valés-Gómez, Vilches, Martín-Gayo, Muñoz-Calleja, Sanchez-Madrid and Alfranca.
Déclaration de conflit d'intérêts
The 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.
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