Strategies using functional genomics in rheumatic diseases

被引:7
作者
Burmester, GR
Häupl, T
机构
[1] Humboldt Univ, Charite Univ Med Berlin, Dept Rheumatol & Clin Immunol, D-10098 Berlin, Germany
[2] Free Univ Berlin, D-10098 Berlin, Germany
关键词
genomics; microarrays; rheumatoid arthritis; spondyloarthritis;
D O I
10.1016/j.autrev.2004.08.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
For functional genomics of inflammatory disorders and infection, rheumatic diseases offer unique features to analyse the transition from infection to chronic inflammation, autoimmunity and immunopathology, both systemic and tissue specific. The diseases are frequent and of considerable socio-economic impact. Well-defined cohorts of patients are available. The tissues and cells involved are readily accessible for molecular analysis. Both genetic predisposition and infection are involved in the aetiopathogenesis of rheumatic diseases. The number of susceptibility and severity genes has been estimated to be at least 30, but only few of them have been identified so far. There is an urgent need for developing new therapies adapted to genetic risk and based on a functional genetic and molecular understanding of chronic inflammation. It is evident that gene analysis in inflammatory rheumatic diseases will not only be beneficial for the large number of patients involved, but will also lead to a better understanding of other inflammatory disorders thereby possibly leading to novel diagnostic and therapeutic strategies in this important group of disorders. (C) 2004 Published by Elsevier B.V.
引用
收藏
页码:541 / 549
页数:9
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