HLA-A homozygosis is associated with susceptibility to COVID-19.

HLA

Instituto de Imunogenética, Associação Fundo de Incentivo à Pesquisa, São Paulo, Brazil.

Published: August 2021

AI Article Synopsis

  • This study examined how specific genetic factors (HLA and ABO polymorphisms) affect the likelihood and severity of COVID-19 in kidney transplant recipients, involving 720 infected individuals and 1680 controls.
  • No strong links between specific HLA types and COVID-19 outcomes were found, but homozygosity at the HLA-A locus showed an increased susceptibility to the virus.
  • Blood groups A and O were found to correlate with susceptibility and resistance to COVID-19, respectively, while older age and pre-existing heart conditions were the main factors impacting the severity of the disease.

Article Abstract

The purpose of this single center retrospective study was to investigate the relationship between HLA and ABO polymorphisms and COVID-19 susceptibility and severity in kidney transplant recipients. It included 720 recipients who had COVID-19 and 1680 controls composed by recipients in follow-up who did not contact the transplantation center for COVID-19 symptoms, up to the moment of their inclusion in the study. HLA-A, -B, and -DRB1 allele groups and ABO frequencies were compared between recipients with COVID-19 (all cases, or separately mild/moderate and severe disease) and controls. The HLA association study was conducted in two case-control series and only associations that showed a p-value <0.05 in both series were considered. No HLA association regarding COVID-19 occurrence or severity met this criterion. Homozygosity at HLA-A locus was associated with COVID-19 susceptibility (odds ratio 1.4) but not severity. Blood groups A and O were associated with susceptibility and resistance to COVID-19, respectively. COVID-19 severity was associated only with older age and cardiac disease, in a multivariate analysis. We conclude that an influence of HLA on COVID-19 susceptibility is supported by the association with homozygosity at HLA-A locus but that there is no evidence for a role of any particular HLA-A, -B, or -DRB1 polymorphism. Thus, we suggest that what matters is the overall capability of an individual's HLA molecules to present SARS-CoV-2 peptides to T cells, a factor that might have a great influence on the breadth of the immune response.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446943PMC
http://dx.doi.org/10.1111/tan.14349DOI Listing

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