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J Autoimmun ; 24(3): 227-33, 2005 May.
Article in English | MEDLINE | ID: mdl-15848045

ABSTRACT

Considerable genetic evidence exit for ANCA-associated vasculitis and pathogenesis. HLA A and B alleles identified serologically from 84 ANCA-positive patients were compared with 101 controls. Further subtyping were done in the 27 "pauci-immune" vasculitis patients using the polymerase chain reaction based PCR-SSOP technique and compared with controls (67). The results revealed that HLA A1 (OR=4.00; p value 2.72E-05), B17 (OR=3.38; p value 0.0008) and HLA B40 (OR=2.74; p value 0.001) were significantly increased among ANCA-positive patients when compared with the controls. Further, the molecular subtypes A*0101 (OR=5.04; p value 0.0005), B*5801 (OR=4.47; p value 0.0002) and haplotype A*0101-B*5801 (OR=4.47; p value 0.0001) were significantly increased among the autoimmune patients. The study revealed that HLA A1, B17 and B40 alleles are associated in production of antineutrophil autoantibodies and A*0101-B*5801 haplotype is significantly associated with autoimmune diseases and they may be invariably involved in disease pathogenesis in India.


Subject(s)
Antibodies, Antineutrophil Cytoplasmic/blood , HLA-A1 Antigen/genetics , HLA-B Antigens/genetics , Antibodies, Antineutrophil Cytoplasmic/genetics , Autoimmune Diseases/genetics , Autoimmune Diseases/immunology , HLA-B40 Antigen , Humans , Immunogenetics , India , Leprosy/genetics , Leprosy/immunology , Malaria/genetics , Malaria/immunology , Vasculitis/genetics , Vasculitis/immunology
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