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Published on: June 10, 2025
[Association of HLA-DM gene with childhood systemic lupus erythematosus]
Jun-mei Zhang1, Cai-feng Li, Xiao-hu He
1Department of Rheumatology & Immunology, Beijing Children's Hospital Affiliated to Capital Medical University, Beijing 100045, China.
Insights
The HLA-DM gene
Area of Science:
- Immunogenetics
- Rheumatology
- Pediatric Autoimmunity
Context:
- Childhood-onset systemic lupus erythematosus (cSLE) is a complex autoimmune disease.
- Genetic factors play a crucial role in SLE pathogenesis.
- The human leukocyte antigen (HLA) system, particularly HLA-DM, is implicated in immune regulation.
Purpose:
- To investigate the association between specific Human Leukocyte Antigen - DM (HLA-DM) gene variants and the susceptibility to childhood systemic lupus erythematosus (SLE).
- To determine if particular HLA-DM alleles are linked to disease presentation or organ involvement in pediatric SLE patients.
Summary:
- Sequence-based typing identified specific HLA-DM genotypes in 79 pediatric SLE patients and 57 controls.
- A significantly lower frequency of DMB*0101/0102 was observed in SLE patients compared to controls.
- Conversely, the DMB*0102/0102 genotype was more prevalent in SLE patients with renal involvement, suggesting a dual role.
Impact:
- The findings suggest HLA-DM, specifically the DMB*0102/0102 allele, may act as a protective factor against SLE development.
- This allele may also confer susceptibility to renal complications in pediatric SLE patients.
- Understanding these genetic associations can inform future diagnostic and therapeutic strategies for childhood SLE.
Objective:
To explore the association of HLA-DM gene with childhood systemic lupus erythematosus (SLE).
Methods:
DMA and DMB genes were genotyped by sequence-based typing(SBT)in 79 SLE patients at our hospital from 2003 to 2006 and 57 normal controls.
Results:
The frequency of DMB*0101/0102 was lower significantly in SLE patients than that in controls (5.1% vs 21.1%). And the frequency of DMB*0102/0102 in SLE patients with renal involvement was higher than that in controls (17.6% vs 1.8%, P < 0.05). The frequency of all alleles and other genotypes had no significance in SLE patients, SLE patients with different organ involvements and controls.
Conclusion:
As a protective gene, DMB*0102/0102 may be a susceptible allele for SLE patients with renal involvement.
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