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

Renato De Marco1, Tathyane C Faria1, Karina L Mine1

  • 1Instituto de Imunogenética, Associação Fundo de Incentivo à Pesquisa, São Paulo, Brazil.

HLA
|June 24, 2021
PubMed

Insights

In kidney transplant recipients, HLA homozygosity at the HLA-A locus may increase COVID-19 susceptibility, while specific HLA-A, -B, or -DRB1 types do not influence disease severity. Blood group A was linked to susceptibility and O to resistance.

Area of Science:

  • Immunogenetics
  • Transplantation Immunology
  • Infectious Diseases

Background:

  • Kidney transplant recipients are a vulnerable population for infections, including COVID-19.
  • Understanding genetic factors like HLA and ABO polymorphisms may reveal insights into COVID-19 susceptibility and severity in this group.

Purpose of the Study:

  • To investigate the association between Human Leukocyte Antigen (HLA) and ABO blood group polymorphisms and COVID-19 susceptibility and severity in kidney transplant recipients.

Main Methods:

  • Retrospective case-control study involving 720 kidney transplant recipients with COVID-19 and 1680 controls.
  • Comparison of HLA-A, -B, -DRB1 allele groups and ABO frequencies between COVID-19 cases and controls.
  • Statistical analysis, including multivariate analysis, to identify significant associations.

Main Results:

  • No specific HLA-A, -B, or -DRB1 allele group associations with COVID-19 occurrence or severity were found.
  • Homozygosity at the HLA-A locus was associated with increased COVID-19 susceptibility (OR 1.4).
  • Blood group A showed association with susceptibility, while blood group O was associated with resistance to COVID-19.

Conclusions:

  • While homozygosity at the HLA-A locus may influence COVID-19 susceptibility in kidney transplant recipients, specific HLA polymorphisms do not appear to affect disease severity.
  • The overall capability of HLA molecules to present viral peptides may be more critical than specific alleles for T-cell mediated immune response breadth.

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