Kinase inhibitors: The next generation of therapies in the treatment of rheumatoid arthritis

被引:40
|
作者
Macfarlane, Lindsey A. [1 ]
Todd, Derrick J. [1 ,2 ]
机构
[1] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Div Rheumatol Immunol & Allergy, Boston, MA 02115 USA
关键词
kinase inhibitors; rheumatoid arthritis; tofacitinib; treatment; PLACEBO-CONTROLLED TRIAL; MODIFYING ANTIRHEUMATIC DRUGS; ANTITUMOR NECROSIS FACTOR; SYK TYROSINE KINASE; TOFACITINIB CP-690,550; DOUBLE-BLIND; INADEQUATE RESPONSE; JAK INHIBITOR; CONCOMITANT METHOTREXATE; RECEIVING METHOTREXATE;
D O I
10.1111/1756-185X.12293
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rheumatoid arthritis (RA) can be the source of significant pain and functional limitation. The past 20years have seen a transition in treatment goals away from mere pain management toward disease modification through the suppression of autoimmunity. Disease-modifying anti-rheumatic drugs, such as methotrexate and biologic agents, impair disease progression and joint destruction. However, despite these achievements, a substantial subset of RA patients does not respond to or cannot tolerate current treatments for RA. Scientific insight into the cellular pathways of inflammation has revealed new therapeutic targets for the treatment of autoimmune diseases like RA. Attention has focused on pathways mediated by Janus kinase (JAK), mitogen-activated protein kinase (MAPK), and spleen tyrosine kinase (Syk). This review article summarizes the evidence supporting the use of various kinase inhibitors, including the newly approved JAK inhibitor tofacitinib, in the treatment of RA.
引用
收藏
页码:359 / 368
页数:10
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