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Association between HLA gene polymorphisms and mortality of COVID‐19: An in silico analysis
INTRODUCTION: The emergence of SARS‐CoV‐2 has caused global public health and economic crisis. Human leukocyte antigen (HLA) is a critical component of the viral antigen presentation pathway and plays essential roles in conferring differential viral susceptibility and severity of diseases. However,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7654404/ https://www.ncbi.nlm.nih.gov/pubmed/33047883 http://dx.doi.org/10.1002/iid3.358 |
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author | Tomita, Yusuke Ikeda, Tokunori Sato, Ryo Sakagami, Takuro |
author_facet | Tomita, Yusuke Ikeda, Tokunori Sato, Ryo Sakagami, Takuro |
author_sort | Tomita, Yusuke |
collection | PubMed |
description | INTRODUCTION: The emergence of SARS‐CoV‐2 has caused global public health and economic crisis. Human leukocyte antigen (HLA) is a critical component of the viral antigen presentation pathway and plays essential roles in conferring differential viral susceptibility and severity of diseases. However, the association between HLA gene polymorphisms and risk for COVID‐19 has not been fully elucidated. We hypothesized that HLA genotypes might impact on the differences in morbidity and mortality of COVID‐19 across countries. METHODS: We conducted in silico analyses and examined an association of HLA gene polymorphisms with prevalence and mortality of COVID‐19 by using publicly available databases. RESULTS: We found that a possible association between HLA‐A*02:01 and an increased risk for COVID‐19. HLA‐A*02:01 had a relatively lower capacity to present SARS‐CoV‐2 antigens compared with other frequent HLA class I molecules, HLA‐A*11:01 or HLA‐A*24:02. CONCLUSION: This study suggests that individuals with HLA‐A*11:01 or HLA‐A*24:02 genotypes may generate efficiently T‐cell‐mediated antiviral responses to SARS‐CoV‐2 compared with HLA‐A*02:01. The differences in HLA genotypes may potentially alter the course of the disease and its transmission. |
format | Online Article Text |
id | pubmed-7654404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76544042020-11-16 Association between HLA gene polymorphisms and mortality of COVID‐19: An in silico analysis Tomita, Yusuke Ikeda, Tokunori Sato, Ryo Sakagami, Takuro Immun Inflamm Dis Original Research INTRODUCTION: The emergence of SARS‐CoV‐2 has caused global public health and economic crisis. Human leukocyte antigen (HLA) is a critical component of the viral antigen presentation pathway and plays essential roles in conferring differential viral susceptibility and severity of diseases. However, the association between HLA gene polymorphisms and risk for COVID‐19 has not been fully elucidated. We hypothesized that HLA genotypes might impact on the differences in morbidity and mortality of COVID‐19 across countries. METHODS: We conducted in silico analyses and examined an association of HLA gene polymorphisms with prevalence and mortality of COVID‐19 by using publicly available databases. RESULTS: We found that a possible association between HLA‐A*02:01 and an increased risk for COVID‐19. HLA‐A*02:01 had a relatively lower capacity to present SARS‐CoV‐2 antigens compared with other frequent HLA class I molecules, HLA‐A*11:01 or HLA‐A*24:02. CONCLUSION: This study suggests that individuals with HLA‐A*11:01 or HLA‐A*24:02 genotypes may generate efficiently T‐cell‐mediated antiviral responses to SARS‐CoV‐2 compared with HLA‐A*02:01. The differences in HLA genotypes may potentially alter the course of the disease and its transmission. John Wiley and Sons Inc. 2020-10-13 /pmc/articles/PMC7654404/ /pubmed/33047883 http://dx.doi.org/10.1002/iid3.358 Text en © 2020 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Tomita, Yusuke Ikeda, Tokunori Sato, Ryo Sakagami, Takuro Association between HLA gene polymorphisms and mortality of COVID‐19: An in silico analysis |
title | Association between HLA gene polymorphisms and mortality of COVID‐19: An in silico analysis |
title_full | Association between HLA gene polymorphisms and mortality of COVID‐19: An in silico analysis |
title_fullStr | Association between HLA gene polymorphisms and mortality of COVID‐19: An in silico analysis |
title_full_unstemmed | Association between HLA gene polymorphisms and mortality of COVID‐19: An in silico analysis |
title_short | Association between HLA gene polymorphisms and mortality of COVID‐19: An in silico analysis |
title_sort | association between hla gene polymorphisms and mortality of covid‐19: an in silico analysis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7654404/ https://www.ncbi.nlm.nih.gov/pubmed/33047883 http://dx.doi.org/10.1002/iid3.358 |
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