Interleukin-10 promoter polymorphisms in myasthenia gravis

被引:16
作者
Alseth, Espen Homleid [2 ]
Nakkestad, Hanne Linda [2 ]
Aarseth, Jan [2 ]
Gilhus, Nils Erik [1 ,2 ]
Skeie, Geir Olve [1 ,2 ]
机构
[1] Haukeland Hosp, Dept Neurol, N-5021 Bergen, Norway
[2] Univ Bergen, Dept Clin Med, N-5020 Bergen, Norway
关键词
Myasthenia gravis; IL-10 promoter polymorphism; Genetics; BLOOD MONONUCLEAR-CELLS; RHEUMATOID-ARTHRITIS; RYANODINE RECEPTOR; IL-10; LOCUS; TNF-ALPHA; T-CELLS; ANTIBODIES; REGION; TITIN; GENE;
D O I
10.1016/j.jneuroim.2009.02.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Interleukin 10 (IL-10) is secreted by several hemopoietic cells and suppresses the Th1 mediated immune response, while stimulating B cell differentiation and the humoral immune response. IL-10 expression in Con A-stimulated peripheral blood mononuclear cells is related to three polymorphisms in the promoter region of the IL-10 gene; G/A at position -1082, T/C at position -819 and A/C at position -592. We analyzed the distribution of these IL-10 polymorphisms in 64 MG patients and 87 healthy blood donors to determine any influence on MG susceptibility. MG patients had a significantly higher frequency of the ACC/ACC haplotype (12.5% vs 3.4% in controls), as had the subgroups with late onset MG and thymomatous MG (20.0% and 21.4%, respectively). Early onset MG patients had a high frequency of the ATA/ATA haplotype (19.2% vs 3.4% in controls). Titin Ab-positive MG patients had high ACC/ACC (20.0%). This study indicates a direct link between IL-10 and MG pathogenesis, although the complex role of this multi-faceted cytokine in vivo is as yet not fully elucidated. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:63 / 66
页数:4
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