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Biological targets in the treatment of rheumatoid arthritis: a comprehensive review of current and in-development biological disease modifying anti-rheumatic drugs.

作者信息

Kukar Manil, Petryna Olga, Efthimiou Petros

机构信息

Rheumatology Division, Lincoln Medical and Mental Health Center, New York, NY, USA.

出版信息

Biologics. 2009;3:443-57. Epub 2009 Oct 12.

PMID:19851470
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2763315/
Abstract

Enhanced understanding of the rheumatoid arthritis (RA) pathophysiology and the role of cytokines has enabled the development of innovative biological agents in the last 10 years that target specific parts of the immune response. Failure to achieve adequate response with traditional disease modifying anti-rheumatic drugs (DMARDs) and increasing evidence of ongoing radiographic deterioration of the affected joints despite seemingly clinical response were essential stimuli for the development of biologics. The current and upcoming biological agents are primarily aimed at neutralizing circulating and cell-bound pro-inflammatory cytokines, interfering in the interaction of antigen-presenting and T-lymphocytes, eliminating circulating B-lymphocytes or by interfering with the intracellular signaling mechanisms of immuno-competent cells that lead to inflammation. These agents have improved the currently available treatments due to greater efficacy, fast action and greater tolerability. However, use of these agents has also been associated with significant, although rare, adverse events and considerable cost. Therefore, these agents should be used with caution by experienced clinicians. The present work aims to provide a global and updated review of the current and in-development biological DMARDs for the treatment of RA.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ae2/2763315/80e8da424d55/btt-3-443f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ae2/2763315/5415d3dbc730/btt-3-443f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ae2/2763315/80e8da424d55/btt-3-443f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ae2/2763315/5415d3dbc730/btt-3-443f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ae2/2763315/80e8da424d55/btt-3-443f2.jpg

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本文引用的文献

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Anakinra for rheumatoid arthritis: a systematic review.阿那白滞素治疗类风湿关节炎:一项系统评价。
J Rheumatol. 2009 Jun;36(6):1118-25. doi: 10.3899/jrheum.090074. Epub 2009 May 15.
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New tumour necrosis factor inhibitors for rheumatoid arthritis: are there benefits from extending choice?用于类风湿性关节炎的新型肿瘤坏死因子抑制剂:扩大选择范围会带来益处吗?
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靶向跨膜蛋白-蛋白相互作用:数百万年历史的新型治疗策略。
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Costs associated with rheumatoid arthritis in Italy: past, present, and future.意大利类风湿关节炎相关费用:过去、现在与未来。
Clinicoecon Outcomes Res. 2016 Feb 10;8:33-41. doi: 10.2147/CEOR.S91006. eCollection 2016.
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Antigen-specific gene therapy after immunisation reduces the severity of collagen-induced arthritis.免疫后进行抗原特异性基因治疗可减轻胶原诱导性关节炎的严重程度。
Clin Dev Immunol. 2013;2013:345092. doi: 10.1155/2013/345092. Epub 2013 Nov 26.
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