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Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection.

Authors :
Marchal A
Cirulli ET
Neveux I
Bellos E
Thwaites RS
Schiabor Barrett KM
Zhang Y
Nemes-Bokun I
Kalinova M
Catchpole A
Tangye SG
Spaan AN
Lack JB
Ghosn J
Burdet C
Gorochov G
Tubach F
Hausfater P
Dalgard CL
Zhang SY
Zhang Q
Chiu C
Fellay J
Grzymski JJ
Sancho-Shimizu V
Abel L
Casanova JL
Cobat A
Bolze A
Source :
HGG advances [HGG Adv] 2024 Jul 18; Vol. 5 (3), pp. 100300. Date of Electronic Publication: 2024 Apr 26.
Publication Year :
2024

Abstract

Human genetic studies of critical COVID-19 pneumonia have revealed the essential role of type I interferon-dependent innate immunity to SARS-CoV-2 infection. Conversely, an association between the HLA-B∗15:01 allele and asymptomatic SARS-CoV-2 infection in unvaccinated individuals was recently reported, suggesting a contribution of pre-existing T cell-dependent adaptive immunity. We report a lack of association of classical HLA alleles, including HLA-B∗15:01, with pre-omicron asymptomatic SARS-CoV-2 infection in unvaccinated participants in a prospective population-based study in the United States (191 asymptomatic vs. 945 symptomatic COVID-19 cases). Moreover, we found no such association in the international COVID Human Genetic Effort cohort (206 asymptomatic vs. 574 mild or moderate COVID-19 cases and 1,625 severe or critical COVID-19 cases). Finally, in the Human Challenge Characterisation study, the three HLA-B∗15:01 individuals infected with SARS-CoV-2 developed symptoms. As with other acute primary infections studied, no classical HLA alleles favoring an asymptomatic course of SARS-CoV-2 infection were identified.<br />Competing Interests: Declaration of interests E.T.C., K.M.S.B., and A.B. are employees of Helix.<br /> (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
2666-2477
Volume :
5
Issue :
3
Database :
MEDLINE
Journal :
HGG advances
Publication Type :
Academic Journal
Accession number :
38678364
Full Text :
https://doi.org/10.1016/j.xhgg.2024.100300