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Impaired Priming of SARS-CoV-2-Specific Naive CD8 + T Cells in Older Subjects.

Authors :
Gallerani E
Proietto D
Dallan B
Campagnaro M
Pacifico S
Albanese V
Marzola E
Marconi P
Caputo A
Appay V
Gavioli R
Nicoli F
Source :
Frontiers in immunology [Front Immunol] 2021 Jul 13; Vol. 12, pp. 693054. Date of Electronic Publication: 2021 Jul 13 (Print Publication: 2021).
Publication Year :
2021

Abstract

Advanced age is associated with severe symptoms and death upon SARS-CoV-2 infection. Virus-specific CD8 <superscript>+</superscript> T-cell responses have shown to be protective toward critical COVID-19 manifestations, suggesting that suboptimal cellular immunity may contribute to the age-pattern of the disease. The induction of a CD8 <superscript>+</superscript> T-cell response against an emerging pathogen like SARS-CoV-2 relies on the activation of naive T cells. To investigate whether the primary CD8 <superscript>+</superscript> T-cell response against this virus is defective in advanced age, we used an in vitro approach to prime SARS-CoV-2-specific naive CD8 <superscript>+</superscript> T cells from healthy, unexposed donors of different age groups. Compared to younger adults, older individuals display a poor SARS-CoV-2-specific T-cell priming capacity in terms of both magnitude and quality of the response. In addition, older subjects recognize a lower number of epitopes. Our results implicate that immune aging is associated with altered primary SARS-CoV-2-specific CD8 <superscript>+</superscript> T-cell responses.<br />Competing Interests: 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.<br /> (Copyright © 2021 Gallerani, Proietto, Dallan, Campagnaro, Pacifico, Albanese, Marzola, Marconi, Caputo, Appay, Gavioli and Nicoli.)

Details

Language :
English
ISSN :
1664-3224
Volume :
12
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
34326844
Full Text :
https://doi.org/10.3389/fimmu.2021.693054