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Autoimmune-associated HLA-B8-DR3 haplotypes in Asian Indians are unique in C4 complement gene copy numbers and HSP-2
Gurvinder Kaur1, Neeraj Kumar, Agnes Szilagyi
1Department of Transplant Immunology and Immunogenetics, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.
Insights
Asian Indian B8-DR3 haplotypes, distinct from Caucasian AH8.1, show unique genetic variations. These differences suggest independent origins and a potential shared genetic factor in autoimmune disease associations.
Area of Science:
- Immunogenetics
- Human Leukocyte Antigen (HLA) complex
- Autoimmune disease genetics
Background:
- The classical AH8.1 (HLA-A1-B8-DR3-DQ2) haplotype is prevalent in Caucasians and linked to autoimmune diseases.
- Asian Indians exhibit unique B8-DR3 haplotypes, designated as AH8.1 variants, also associated with autoimmunity.
Purpose of the Study:
- To compare complement component 4A (C4A) and C4B copy numbers in Indian and Caucasian B8-DR3 haplotypes.
- To identify alleles within the heat shock protein 70-2 (HSP70-2) and lymphotoxin-alpha (LTA) genes in these haplotypes.
Main Methods:
- Comparative analysis of C4A and C4B gene copy numbers.
- Allele identification for HSP70-2 and LTA genes using genetic typing.
- Analysis of Bf and Tumor Necrosis Factor (TNF) gene variations.
Main Results:
- Indian B8-DR3 haplotypes possess one copy each of C4A and C4B, unlike Caucasian AH8.1 (one C4B, no C4A).
- Distinct HSP70-2 alleles (*A in Indian, *G in Caucasian) were observed.
- Shared LTA 252 *G allele found in both populations; Indian haplotypes had Bf*F and TNF-308*G, differing from Caucasian Bf*S and TNF-308*A.
Conclusions:
- Genetic variations in C4A, HSP70-2, Bf, and TNF suggest independent origins for Indian and Caucasian B8-DR3-DQ2 haplotypes.
- Shared autoimmune disease associations across diverse haplotypes indicate a potential common genetic component driving these conditions.
Abstract:
The classical AH8.1 (HLA-A1-B8-DR3-DQ2) is the most common Caucasian haplotype, associated with several autoimmune diseases, immunologic hyperreactivity and rapid progression to the acquired immunodeficiency syndrome. However, in Asian Indians, there are multiple unique B8-DR3 haplotypes that are associated with autoimmunity and differ significantly from the common Caucasian AH8.1. The Indian HLA-A1-B8-DR3 is therefore referred to as an AH8.1 variant. The aims of this study were to compare C4A and C4B copy numbers and to identify alleles in HSP70-2 and LTA in these haplotypes. The Indian B8-DR3 haplotypes differ from the Caucasian AH8.1 at C4A and HSP70-2 loci. The Indian B8-DR3 haplotypes have 1 copy each at C4A and C4B, while the Caucasian AH8.1 has 1 copy at C4B but no C4A gene. Moreover, the Indian and Caucasian B8-DR3 haplotypes had HSP70-2 1267 *A, and *G alleles, respectively. By contrast, the LTA 252 *G allele occurred both in the Indian and Caucasian haplotypes. The Indian haplotypes also contained Bf*F and TNF-308*G that were different from the Caucasian equivalents Bf*S and TNF-308*A. These differences and previous studies support the hypothesis that B8-DR3-DQ2 haplotypes in Asian Indian population might have originated independently of Caucasian AH8.1 selectively through recombination and mutations. Because autoimmune disease associations are shared among these otherwise diverse haplotypes, these data strongly suggest that some shared component(s) of all these associated haplotypes may be playing a key role in such associations.
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