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Perturbations of the T-cell receptor repertoire in response to SARS-CoV-2 in immunocompetent and immunocompromised individuals.

Authors :
Delmonte OM
Oguz C
Dobbs K
Myint-Hpu K
Palterer B
Abers MS
Draper D
Truong M
Kaplan IM
Gittelman RM
Zhang Y
Rosen LB
Snow AL
Dalgard CL
Burbelo PD
Imberti L
Sottini A
Quiros-Roldan E
Castelli F
Rossi C
Brugnoni D
Biondi A
Bettini LR
D'Angio M
Bonfanti P
Anderson MV
Saracino A
Chironna M
Di Stefano M
Fiore JR
Santantonio T
Castagnoli R
Marseglia GL
Magliocco M
Bosticardo M
Pala F
Shaw E
Matthews H
Weber SE
Xirasagar S
Barnett J
Oler AJ
Dimitrova D
Bergerson JRE
McDermott DH
Rao VK
Murphy PM
Holland SM
Lisco A
Su HC
Lionakis MS
Cohen JI
Freeman AF
Snyder TM
Lack J
Notarangelo LD
Source :
The Journal of allergy and clinical immunology [J Allergy Clin Immunol] 2024 Jun; Vol. 153 (6), pp. 1655-1667. Date of Electronic Publication: 2023 Dec 27.
Publication Year :
2024

Abstract

Background: Functional T-cell responses are essential for virus clearance and long-term protection after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, whereas certain clinical factors, such as older age and immunocompromise, are associated with worse outcome.<br />Objective: We sought to study the breadth and magnitude of T-cell responses in patients with coronavirus disease 2019 (COVID-19) and in individuals with inborn errors of immunity (IEIs) who had received COVID-19 mRNA vaccine.<br />Methods: Using high-throughput sequencing and bioinformatics tools to characterize the T-cell receptor β repertoire signatures in 540 individuals after SARS-CoV-2 infection, 31 IEI recipients of COVID-19 mRNA vaccine, and healthy controls, we quantified HLA class I- and class II-restricted SARS-CoV-2-specific responses and also identified several HLA allele-clonotype motif associations in patients with COVID-19, including a subcohort of anti-type 1 interferon (IFN-1)-positive patients.<br />Results: Our analysis revealed that elderly patients with COVID-19 with critical disease manifested lower SARS-CoV-2 T-cell clonotype diversity as well as T-cell responses with reduced magnitude, whereas the SARS-CoV-2-specific clonotypes targeted a broad range of HLA class I- and class II-restricted epitopes across the viral proteome. The presence of anti-IFN-I antibodies was associated with certain HLA alleles. Finally, COVID-19 mRNA immunization induced an increase in the breadth of SARS-CoV-2-specific clonotypes in patients with IEIs, including those who had failed to seroconvert.<br />Conclusions: Elderly individuals have impaired capacity to develop broad and sustained T-cell responses after SARS-CoV-2 infection. Genetic factors may play a role in the production of anti-IFN-1 antibodies. COVID-19 mRNA vaccines are effective in inducing T-cell responses in patients with IEIs.<br /> (Published by Elsevier Inc.)

Details

Language :
English
ISSN :
1097-6825
Volume :
153
Issue :
6
Database :
MEDLINE
Journal :
The Journal of allergy and clinical immunology
Publication Type :
Academic Journal
Accession number :
38154666
Full Text :
https://doi.org/10.1016/j.jaci.2023.12.011