Autoimmune diseases induced by TNF-targeted therapies

被引:220
作者
Ramos-Casals, Manuel [1 ]
Brito-Zeron, Pilar
Soto, Maria-Jose
Cuadrado, Maria-Jose [2 ,3 ]
Khamashta, Munther A. [2 ,3 ]
机构
[1] Hosp Clin Barcelona, IDIBAPS, Dept Autoimmune Dis, Lab Autoimmune Dis Josep Font,Serv Malalties Auto, E-08036 Barcelona, Spain
[2] Kings Coll London, St Thomas Hosp, Guys Hosp, Sch Med,Rayne Inst,Lupus Res Unit, London WC2R 2LS, England
[3] Kings Coll London, St Thomas Hosp, Kings Hosp, Sch Med,Rayne Inst,Lupus Res Unit, London WC2R 2LS, England
来源
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY | 2008年 / 22卷 / 05期
关键词
adalimumab; anti-TNF; etanercept; infliximab; interstitial lung disease; lupus; thrombosis; vasculitis;
D O I
10.1016/j.berh.2008.09.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Anti-TNF agents are increasingly being used for a rapidly expanding number of rheumatic and systemic autoimmune diseases. As a result of this use, and of the longer follow-up periods of treatment, there are a growing number of reports of the development of autoimmune processes related to anti-TNF agents. The clinical characteristics, outcomes, and patterns of association with the different anti-TNF agents used in all reports of autoimmune diseases developing after TNF-targeted therapy, were analyzed through a baseline Medline search of articles published between January 1990 and May 2008 (www.biogeas.org). A total of 379 cases of autoimmune diseases secondary to TNF-targeted therapies were identified. The anti-TNF agents were administered for rheumatoid arthritis in more than 80% of cases. The use of anti-TNF agents has been associated with an increasing number of cases of autoimmune diseases, principally cutaneous vasculitis, lupus-like syndrome, systemic lupus erythematosus and interstitial lung disease. Other autoimmune diseases associated with TNF-targeted therapies have been recently described, e.g. sarcoidosis, antiphospholipid syndrome-related features, and autoimmune hepatitis or uveitis. Large, prospective, postmarketing studies are required to evaluate the risk of developing autoimmune diseases in patients receiving TNF-targeted therapies.
引用
收藏
页码:847 / 861
页数:15
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