Open AccessImmunogenetic risk factors for anti‐neutrophil cytoplasmic antibody (ANCA)‐associated systemic vasculitis
Author(s) -
Martin Genčík,
Stefan Borgmann,
R. K. Zahn,
E. D. Albert,
Thomas Sitter,
Jörg T. Epplen,
Harald Fricke
Publication year - 1999
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1046/j.1365-2249.1999.00969.x
Subject(s) - immunology , vasculitis , systemic vasculitis , microscopic polyangiitis , anti neutrophil cytoplasmic antibody , medicine , haplotype , human leukocyte antigen , pathogenesis , genetic predisposition , disease , genotype , biology , gene , genetics , antigen
Wegener's granulomatosis (WG) and microscopic polyangiitis are systemic autoimmune diseases characterized by the presence of ANCA in the sera of patients. Little is known about the aetiologic factors and genetic predisposition as well as the pathogenesis of these disease entities. A slightly decreased representation of HLA‐DRB1*13 and HLA‐DQB1*0603 individuals was observed in our cohort of ANCA‐associated systemic vasculitis (AASV) patients compared with controls. In addition, HLA‐DRB1*04 individuals were over‐represented in a subgroup of patients with WG in end‐stage renal disease as a result of renal vasculitis. In order to identify other genes relevant for these diseases, we investigated highly polymorphic markers in the vicinity of several immunorelevant genes, i.e. tumour necrosis factor ( TNF ) α , IL‐2 , IL‐5 receptor α ( IL‐5RA ), in a group of 102 patients with AASV and compared the representation with controls. Furthermore, functional polymorphisms were directly analysed in the promotor region of TNFα as well as in the coding region of the FcγIIRA genes. Polymorphisms of the TNFα promotor (TNF‐308) as well as in the FcγIIRA gene were excluded as risk factors for the disease in our cohort. No major phenotype distribution differences were observed between patients and controls for the IL‐2 and IL‐5RA microsatellites. Most importantly, several haplotypes on chromosome 6p appeared strongly associated with proteinase 3 (PR3)‐ANCA + AASV. Thus, as in other autoimmune diseases, different predisposing factors play differential aetiopathogenic roles in various groups of AASV patients.