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- Yamaoka Kunihiro
- The First Department of Internal Medicine, University of Occupational and Environmental Health, Fukuoka, Japan
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- Kubo Satoshi
- The First Department of Internal Medicine, University of Occupational and Environmental Health, Fukuoka, Japan
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- Sonomoto Koshiro
- The First Department of Internal Medicine, University of Occupational and Environmental Health, Fukuoka, Japan
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- Maeshima Keisuke
- Department of Internal Medicine I, Faculty of Medicine, Oita University, Oita, Japan
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- Tanaka Yoshiya
- The First Department of Internal Medicine, University of Occupational and Environmental Health, Fukuoka, Japan
抄録
Treatment of rheumatoid arthritis (RA) with biologic agents targeting inflammatory cytokines and cell surface molecules such as tumor necrosis factor and Interleukin-6 is generally more efficacious than traditional disease-modifying antirheumatic drugs when combined with MTX. However, not only do ∼30% of patients poorly respond to treatment but also parenteral mode of administration and expense are issues to be solved. Recently, a kinase inhibitor targeting Janus kinases (JAKs), has shown high efficacy in active RA in clinical trials. Among several JAK inhibitors in clinical trials for RA, tofacitinib is a step ahead for use in clinical practice. Kinase inhibitors are orally available, which is a major advantage over biologic agents, in addition to being less expensive. This review describes recent advance in JAK inhibitors for RA and its possible mechanism of action.
収録刊行物
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- Inflammation and Regeneration
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Inflammation and Regeneration 31 (4), 349-353, 2011
一般社団法人 日本炎症・再生医学会
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詳細情報 詳細情報について
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- CRID
- 1390282680233547776
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- NII論文ID
- 130004482280
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- ISSN
- 18808190
- 18809693
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可