类风湿性关节炎
甲氨蝶呤
医学
免疫学
关节炎
腺苷
体内
内生
药理学
细胞凋亡
癌症研究
内科学
生物
生物化学
生物技术
作者
Judith A.M. Wessels,T. Huizinga,Henk‐Jan Guchelaar
出处
期刊:Rheumatology
[Oxford University Press]
日期:2007-11-28
卷期号:47 (3): 249-255
被引量:327
标识
DOI:10.1093/rheumatology/kem279
摘要
This review presents recent data supporting the methotrexate (MTX) mechanisms of action, which are likely to account for its anti-proliferative and immunosuppressive effects in rheumatoid arthritis (RA). The effects of MTX in vivo may be mediated by reducing cell proliferation, increasing the rate of apoptosis of T cells, increasing endogenous adenosine release, altering the expression of cellular adhesion molecules, influencing production of cytokines, humoral responses and bone formation. Several reports indicate that the effects of MTX are influenced by genetic variants, specific dynamic processes and micro-environmental elements such as nucleotide deprivation or glutathione levels. The challenge for the future will be linking biological and genetic markers relevant to the response to MTX in RA.
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