The role of tumor necrosis factor-alpha in systemic lupus erythematosus

被引:128
作者
Aringer, Martin [1 ]
Smolen, Josef S. [2 ]
机构
[1] Tech Univ Dresden, Univ Clin Ctr Carl Gustav Carus, Dept Med 3, Div Rheumatol, D-01307 Dresden, Germany
[2] Med Univ Vienna, Dept Rheumatol Internal Med 3, A-1090 Vienna, Austria
关键词
D O I
10.1186/ar2341
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Murine models of systemic lupus erythematosus (SLE) have shown apparently contradictory evidence in that either (a) tumor necrosis factor (TNF) expression was low and TNF administration helpful or (b) TNF was high and TNF blockade of therapeutic benefit, depending on the mouse model investigated. In fact, TNF apparently has both effects, checking autoimmunity, at least to some degree, and fostering inflammation. TNF blockade regularly, but transiently, induces or increases autoantibodies to chromatin and to phospholipids. At the same time, open-label data suggest that TNF blockade suppresses inflammatory manifestations of SLE, and long-term benefit was seen in patients with lupus nephritis. A controlled clinical trial is under way.
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