The association of CD18 alleles with anti-myeloperoxidase subtypes of ANCA-associated systemic vasculitides

被引:44
作者
Gencik, M
Meller, S
Borgmann, S
Sitter, T
Saecker, AMM
Fricke, H
Epplen, JT
机构
[1] Ruhr Univ Bochum, D-4630 Bochum, Germany
[2] Univ Munich, Klinikum Innenstadt, Med Klin, D-8000 Munich, Germany
关键词
ANCA; adhesion molecules; immunogenetics; primary systemic vasculitides;
D O I
10.1006/clim.1999.4811
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Wegener granulomatosis (WG), microscopic polyangiitis (MP), and Churg Strauss syndrome (CSS) are rare systemic autoimmune disorders. Common features are anti-neutrophil cytoplasmic antibodies (ANCA) in patient sera. Whereas WG; patients show mainly anti-proteinase 3 ANCA, MP and CSS patients typically present anti-myeloperoxidase (MPO) ANCA. ANCA play an important role in the pathogenesis in the vessel wall by activating polymorphonuclear cells (PMN) and increased adhesivity between PMN and endothelial cells via adhesion molecules. Here we investigated major adhesion molecules as predisposition factors via common polymorphisms in or in the vicinity of the candidate genes ICAM-1, e-selectin, PLAUR, CD11b, and CD18. A restriction fragment-length polymorphism in exon 11 of the CD18 gene was associated with MPO-ANCA(+) systemic vasculitis. Our data indicate that a common variant of the CD18 gene confers increased risk for CSS and MP, supporting that genetic factors are involved in the etiology and pathogenesis of ANCA-associated systemic vasculitides. (C) 2000 Academic Press.
引用
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页码:9 / 12
页数:4
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