Author:
Schetelig Johannes,Heidenreich Falk,Baldauf Henning,Trost Sarah,Falk Bose,Hoßbach Christian,Real Ruben,Roers Axel,Lindemann Dirk,Dalpke Alexander,Kolditz Martin,de With Katja,Bornhäuser Martin,Bonifacio Ezio E.,Rücker-Braun Elke,Lange Vinzenz,Markert Jan,Barth Ralf,Hofmann Jan A.,Sauter Jürgen,Bernas Stefanie N.,Schmidt Alexander H.
Abstract
HLA molecules are key restrictive elements to present intracellular antigens at the crossroads of an effective T-cell response against SARS-CoV-2. To determine the impact of the HLA genotype on the severity of SARS-CoV-2 courses, we investigated data from 6,919 infected individuals. HLA-A, -B, and -DRB1 allotypes grouped into HLA supertypes by functional or predicted structural similarities of the peptide-binding grooves did not predict COVID-19 severity. Further, we did not observe a heterozygote advantage or a benefit from HLA diplotypes with more divergent physicochemical peptide-binding properties. Finally, numbers of in silico predicted viral T-cell epitopes did not correlate with the severity of SARS-CoV-2 infections. These findings suggest that the HLA genotype is no major factor determining COVID-19 severity. Moreover, our data suggest that the spike glycoprotein alone may allow for abundant T-cell epitopes to mount robust T-cell responses not limited by the HLA genotype.
Funder
Bundesministerium für Bildung und Forschung
Subject
Immunology,Immunology and Allergy
Cited by
15 articles.
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