Lack of association between HLA and asymptomatic SARS-CoV-2 infection
Author:
Marchal Astrid, Cirulli Elizabeth T., Neveux Iva, Bellos Evangelos, Thwaites Ryan S., Barrett Kelly M. Schiabor, Zhang Yu, Nemes-Bokun Ivana, Kalinova Mariya, Catchpole Andrew, Tangye Stuart G., Spaan András N., Lack Justin B., Ghosn Jade, Burdet Charles, Gorochov Guy, Tubach Florence, Hausfater Pierre, Dalgard Clifton L., Zhang Shen-Ying, Zhang Qian, Chiu Christopher, Fellay Jacques, Grzymski Joseph J., Sancho-Shimizu Vanessa, Abel Laurent, Casanova Jean-Laurent, Cobat AurélieORCID, Bolze Alexandre, , , , , , , , ,
Abstract
AbstractHuman 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 US (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, no classical HLA alleles favoring an asymptomatic course of SARS-CoV-2 infection were identified. These findings suggest that memory T-cell immunity to seasonal coronaviruses does not strongly influence the outcome of SARS-CoV-2 infection in unvaccinated individuals.
Publisher
Cold Spring Harbor Laboratory
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