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Human Leukocyte Antigen Susceptibility Map for Severe Acute Respiratory Syndrome Coronavirus 2.
Nguyen, Austin; David, Julianne K; Maden, Sean K; Wood, Mary A; Weeder, Benjamin R; Nellore, Abhinav; Thompson, Reid F.
Afiliação
  • Nguyen A; Computational Biology Program, Oregon Health & Science University, Portland, Oregon, USA.
  • David JK; Department of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
  • Maden SK; Computational Biology Program, Oregon Health & Science University, Portland, Oregon, USA.
  • Wood MA; Department of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
  • Weeder BR; Computational Biology Program, Oregon Health & Science University, Portland, Oregon, USA.
  • Nellore A; Department of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
  • Thompson RF; Computational Biology Program, Oregon Health & Science University, Portland, Oregon, USA.
J Virol ; 94(13)2020 06 16.
Article em En | MEDLINE | ID: mdl-32303592
ABSTRACT
Genetic variability across the three major histocompatibility complex (MHC) class I genes (human leukocyte antigen A [HLA-A], -B, and -C genes) may affect susceptibility to and severity of the disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus responsible for coronavirus disease 2019 (COVID-19). We performed a comprehensive in silico analysis of viral peptide-MHC class I binding affinity across 145 HLA-A, -B, and -C genotypes for all SARS-CoV-2 peptides. We further explored the potential for cross-protective immunity conferred by prior exposure to four common human coronaviruses. The SARS-CoV-2 proteome was successfully sampled and was represented by a diversity of HLA alleles. However, we found that HLA-B*4601 had the fewest predicted binding peptides for SARS-CoV-2, suggesting that individuals with this allele may be particularly vulnerable to COVID-19, as they were previously shown to be for SARS (M. Lin, H.-T. Tseng, J. A. Trejaut, H.-L. Lee, et al., BMC Med Genet 49, 2003, https//bmcmedgenet.biomedcentral.com/articles/10.1186/1471-2350-4-9). Conversely, we found that HLA-B*1503 showed the greatest capacity to present highly conserved SARS-CoV-2 peptides that are shared among common human coronaviruses, suggesting that it could enable cross-protective T-cell-based immunity. Finally, we reported global distributions of HLA types with potential epidemiological ramifications in the setting of the current pandemic.IMPORTANCE Individual genetic variation may help to explain different immune responses to a virus across a population. In particular, understanding how variation in HLA may affect the course of COVID-19 could help identify individuals at higher risk from the disease. HLA typing can be fast and inexpensive. Pairing HLA typing with COVID-19 testing where feasible could improve assessment of severity of viral disease in the population. Following the development of a vaccine against SARS-CoV-2, the virus that causes COVID-19, individuals with high-risk HLA types could be prioritized for vaccination.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia Viral / Teste de Histocompatibilidade / Infecções por Coronavirus / Betacoronavirus Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia Viral / Teste de Histocompatibilidade / Infecções por Coronavirus / Betacoronavirus Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article