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.

Human Immunology
|July 29, 2008
PubMed

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.

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