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Published on: August 31, 2014
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.
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.
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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