# Association of human leukocyte antigen B genotypes with COVID-19 severity in Egyptian patients

**Authors:** Reham Abdelmonem, Heba Selim, Shymaa Abdullah Mohamed, Richard Donkor Amponsah, Mohamed Nabil Roshdy, Mona Hassan Hashish

PMC · DOI: 10.1038/s41598-026-36948-7 · Scientific Reports · 2026-02-17

## TL;DR

This study explores how specific HLA-B genes in Egyptian patients affect the severity of COVID-19, finding that certain alleles are linked to more severe cases.

## Contribution

The study identifies HLA-B alleles associated with severe COVID-19 outcomes in an Egyptian population, offering insights into genetic risk factors.

## Key findings

- HLA-B44 and HLA-B08 alleles were significantly associated with severe COVID-19 cases.
- Lower cycle threshold (Ct) values correlated with more severe disease severity.
- HLA-B genotypes may influence viral load and disease progression in SARS-CoV-2 infections.

## Abstract

Host genetic factors, specifically major histocompatibility complex (MHC) influence the prognosis of COVID-19 infections. It plays a central role in the body’s ability to recognize and respond to pathogens, including viruses like SARS-CoV-2. This study aims to identify the significant human leukocyte antigen B (HLA-B) allele genotypes associated with severe cases among SARS-CoV-2-positive patients attending the PCR unit in The Fever Hospital-Alexandria, Egypt. This cross-sectional study was conducted from November 2022 through April 2023. Two swabs (nasopharyngeal and oropharyngeal) were collected from each patient for RT-PCR to determine the cycle threshold (Ct) value. Subsequently, 2 ml of EDTA blood was drawn from each patient for DNA extraction and HLA-B typing using the INNO-LiPA HLA-B Update Plus kit. Patients were divided according to the severity of their infection: mild (N = 15, mean Ct = 26.27 ± 1.27), moderate (N = 15, mean Ct = 24.20 ± 1.63), and severe (N = 15, mean Ct = 22.27 ± 0.93). Ct values were the lowest amongst the severe group with a mean of 22.27 (p = 0.026). Regarding the severity of SAR-CoV-2 infection, 39 HLA-B genotypes, 6 HLA-B super-types, and 22 HLA-B alleles were identified. HLA-B44 was the most significant allele when comparing the three groups of severity: mild, moderate, and severe (p = 0.044). HLA-B08 and HLA-B44 had a statistical significance of (p = 0.011) and (p = 0.034) respectively when comparing the mild group to hospitalized group (severe + moderate). The Ct value is a clear predictor of SARS-CoV-2 severity. HLA-B44 and HLA-B08 were the most significant alleles associated with severe cases, emphasizing the association of human leukocyte antigen B alleles with disease severity and viral load in determining COVID-19 outcomes. These findings may contribute to the development of personalized medical management and improve strategies for COVID-19 control and prevention.

The online version contains supplementary material available at 10.1038/s41598-026-36948-7.

## Linked entities

- **Genes:** HLA-B (major histocompatibility complex, class I, B) [NCBI Gene 3106]
- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}, HLA-B (major histocompatibility complex, class I, B) [NCBI Gene 3106] {aka AS, B-4901, HLAB}, N (nucleocapsid phosphoprotein) [NCBI Gene 43740575], CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, ORF1ab (ORF1a polyprotein;ORF1ab polyprotein) [NCBI Gene 43740578], CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, HLA-DPB1 (major histocompatibility complex, class II, DP beta 1) [NCBI Gene 3115] {aka DPB1, HLA-DP, HLA-DP1B, HLA-DPB}
- **Diseases:** asthma (MESH:D001249), lung consolidation (MESH:D008171), lymphopenia (MESH:D008231), diabetes mellitus (MESH:D003920), inflammatory (MESH:D007249), hypoxia (MESH:D000860), Fever (MESH:D005334), chronic lung disease (MESH:D029424), pneumonia (MESH:D011014), opacity (MESH:D003318), infected (MESH:D007239), COVID-19 infections (MESH:D000086382), thrombocytopenia (MESH:D013921), hypertension (MESH:D006973), death (MESH:D003643), GGO (MESH:C000721427), infectious disease (MESH:D003141), LFTs (MESH:D056486), Liver injury (MESH:D017093), Ground (MESH:D007815)
- **Chemicals:** ethidium bromide (MESH:D004996), EDTA (MESH:D004492), saline (MESH:D012965), ethanol (MESH:D000431), water (MESH:D014867), K (MESH:D011188), Na (MESH:D012964), TAE (-), agarose (MESH:D012685)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12921020/full.md

## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC12921020/full.md

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Source: https://tomesphere.com/paper/PMC12921020