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HLA-B*15 predicts survival in Egyptian patients with COVID-19
Ahmed Samir Abdelhafiz1, Asmaa Ali2, Merhan A Fouda1
1Department of Clinical Pathology, National Cancer Institute, Cairo University, Cairo, Egypt.
Insights
Certain Human Leukocyte Antigen (HLA) -B and -C gene variants are linked to COVID-19 severity and survival. The HLA-B*15 allele showed a protective effect against mortality in Egyptian patients.
Area of Science:
- Immunogenetics
- Virology
- Clinical Medicine
Background:
- Genetic variations influence COVID-19 outcomes.
- Human Leukocyte Antigens (HLA) play a role in COVID-19 susceptibility, severity, and prognosis.
Purpose of the Study:
- To identify HLA-B and -C genotypes in Egyptian COVID-19 patients.
- To correlate these genotypes with disease severity, clinical data, and survival outcomes.
Main Methods:
- HLA-B and -C typing was performed using Luminex-based kits on 69 Egyptian COVID-19 patients.
- Clinical data, laboratory results, and survival rates were analyzed.
Main Results:
- Severe COVID-19 was observed in 58% of patients, with 55% mortality in this group.
- HLA-B*41, -B*42, -C*16, and -C*17 alleles were associated with severe disease.
- HLA-B*15, -C*7, and -C*12 alleles were linked to protection against mortality, with HLA-B*15 showing significant survival benefit (P < 0.001).
- Higher leukocytic count, ferritin, and creatinine levels correlated with reduced survival.
Conclusions:
- Specific HLA class I alleles modulate immune responses, influencing COVID-19 severity and outcomes.
- HLA-B*15 may confer protection against COVID-19 mortality in Egyptian patients.
- This is the first study on this topic in Egyptian patients, highlighting the need for further research into HLA-I interactions with immune cells.
Abstract:
Genetic differences among individuals could affect the clinical presentations and outcomes of COVID-19. Human Leukocyte Antigens are associated with COVID-19 susceptibility, severity, and prognosis. This study aimed to identify HLA-B and -C genotypes among 69 Egyptian patients with COVID-19 and correlate them with disease outcomes and other clinical and laboratory data. HLA-B and -C typing was performed using Luminex-based HLA typing kits. Forty patients (58%) had severe COVID-19; 55% of these patients died, without reported mortality in the moderate group. The alleles associated with severe COVID-19 were HLA-B*41, -B*42, -C*16, and -C*17, whereas HLA-B*15, -C*7, and -C*12 were significantly associated with protection against mortality. Regression analysis showed that HLA-B*15 was the only allele associated with predicted protection against mortality, where the likelihood of survival increased with HLA-B*15 (P < 0.001). Patient survival was less likely to occur with higher total leukocytic count, ferritin, and creatinine levels. This study provides interesting insights into the association between HLA class I alleles and protection from or severity of COVID-19 through immune response modulation. This is the first study to investigate this relationship in Egyptian patients. More studies are needed to understand how HLA class I alleles interact and affect Cytotoxic T lymphocytes and natural killer cell function.
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