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[风湿性疾病临床试验的最新进展]

[Recent progress in clinical trials for rheumatic diseases].

作者信息

Tanaka Yoshiya

机构信息

The First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health.

出版信息

Nihon Rinsho. 2009 Mar;67(3):619-25.

PMID:19280942
Abstract

Rheumatoid arthritis (RA) is a chronic, systemic inflammatory disease that causes significant morbidity and mortality. RA patients should be started with DMARD represented by methotrexate (MTX) as early as possible. However, even use of MTX often fails to control disease activity and to prevent structural damage and, thereby, more effective treatment strategies are needed. Since TNF-alpha and IL-6 play a pivotal role in the pathological processes of RA, biologics targeting these cytokines with MTX, have revolutionized the treatment of RA, producing significant improvement in clinical, radiographic and functional outcomes not seen previously. However, even with these drugs the frequency and degree of responses are restricted. Therefore, new agents targeting cell surface molecules which are involved in cellular interaction and/or signaling on immune cells have been emerging, in order to increase response rates and to achieve high frequencies of remission or even cure. Two biologics abatacept, a CTLA4-Ig fusion protein, and rituximab, an anti-CD20 antibody, were launched in US and EU for the treatment of RA and many biologics are under the clinical trials from the similar concept. Thus, certain biologics have brought about paradigm shift in the treatment of rheumatic diseases, but an economical issue remains unsolved. In order to overcome the concern, low molecular weight chemical products have been rethought. Not a few agents targeting intracellular activation signaling in immune cells such as Jak and Syk are under clinical examinations and some of them appear to show wonderful results, which are comparable to biologics in the context of the treatment of rheumatic diseases. The prospects are here.

摘要

类风湿关节炎(RA)是一种慢性全身性炎症性疾病,可导致严重的发病率和死亡率。类风湿关节炎患者应尽早开始使用以甲氨蝶呤(MTX)为代表的改善病情抗风湿药(DMARD)。然而,即使使用甲氨蝶呤,也常常无法控制疾病活动和预防结构损伤,因此需要更有效的治疗策略。由于肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)在类风湿关节炎的病理过程中起关键作用,与甲氨蝶呤联合使用的靶向这些细胞因子的生物制剂彻底改变了类风湿关节炎的治疗方式,在临床、影像学和功能结局方面产生了前所未有的显著改善。然而,即使使用这些药物,反应的频率和程度仍然有限。因此,为了提高反应率并实现高缓解率甚至治愈,靶向参与免疫细胞细胞间相互作用和/或信号传导的细胞表面分子的新型药物不断涌现。两种生物制剂阿巴西普(一种CTLA4-Ig融合蛋白)和利妥昔单抗(一种抗CD20抗体)已在美国和欧盟获批用于治疗类风湿关节炎,许多基于类似概念的生物制剂正在进行临床试验。因此,某些生物制剂已经在风湿病治疗中带来了范式转变,但经济问题仍未解决。为了克服这一担忧,人们重新审视了低分子量化学产品。不少靶向免疫细胞内激活信号(如Jak和Syk)的药物正在进行临床研究,其中一些似乎显示出了出色的效果,在风湿病治疗方面可与生物制剂相媲美。前景就在这里。

相似文献

1
[Recent progress in clinical trials for rheumatic diseases].[风湿性疾病临床试验的最新进展]
Nihon Rinsho. 2009 Mar;67(3):619-25.
2
[Biologics: current therapeutic strategies for rheumatoid arthritis].[生物制剂:类风湿关节炎的当前治疗策略]
Nihon Rinsho. 2007 Jul;65(7):1179-84.
3
[Paradigm shift in the treatment of rheumatoid arthritis by biologics].[生物制剂治疗类风湿关节炎的范式转变]
Rinsho Byori. 2008 Apr;56(4):309-15.
4
[Management for TNF failure].
Nihon Rinsho. 2007 Jul;65(7):1299-307.
5
[New biologic and non biologic disease modifying anti-rheumatic drugs for rheumatoid arthritis].[用于类风湿关节炎的新型生物和非生物疾病改善抗风湿药物]
Nihon Rinsho Meneki Gakkai Kaishi. 2009 Jun;32(3):149-59. doi: 10.2177/jsci.32.149.
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Do we need new treatment that goes beyond tumor necrosis factor blockers for rheumatoid arthritis?对于类风湿性关节炎,我们是否需要超越肿瘤坏死因子阻滞剂的新治疗方法?
Ann N Y Acad Sci. 2005 Jun;1051:799-810. doi: 10.1196/annals.1361.123.
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[Efficacy of new biologics on bone destruction in rheumatoid arthritis].
Clin Calcium. 2009 Mar;19(3):372-80.
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Strategies after the failure of the first anti-tumor necrosis factor alpha agent in rheumatoid arthritis.类风湿关节炎首支肿瘤坏死因子-α拮抗剂治疗失败后的策略。
Autoimmun Rev. 2010 Jun;9(8):574-82. doi: 10.1016/j.autrev.2010.04.002. Epub 2010 Apr 28.
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[Biologicals in the treatment of rheumatic diseases].[生物制剂在风湿性疾病治疗中的应用]
Dtsch Med Wochenschr. 2006 Oct 13;131(41):2279-85. doi: 10.1055/s-2006-951364.
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Targeted therapy in rheumatoid arthritis.类风湿关节炎的靶向治疗
Wien Med Wochenschr. 2006 Jan;156(1-2):53-60. doi: 10.1007/s10354-005-0245-6.

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Glycoconj J. 2012 Aug;29(5-6):305-13. doi: 10.1007/s10719-012-9407-0. Epub 2012 Jun 12.