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超越传统的 DMARDs:将 TNF 调节剂疗法扩展到绝大多数/弱势群体,他们确实需要这些疗法。

Beyond conventional DMARDs: extending TNF-regulant therapies to the vast majority/less privileged who do need them.

机构信息

Therapeutics Research Unit, Department of Medicine, Princess Alexandra Hospital, Woolloongabba, Brisbane, Queensland, Australia.

出版信息

Int J Rheum Dis. 2009 Dec;12(4):299-306. doi: 10.1111/j.1756-185X.2009.01427.x.

DOI:10.1111/j.1756-185X.2009.01427.x
PMID:20374366
Abstract

This article is a plea to find (better) ways to extend the benefits of anti-cytokine therapies to ensure they will become available as widely as possible. Pessimistically, this will probably involve substituting more affordable, although somewhat less specific, non-biological agents for present target-specific bio-DMARDs (disease-modifying antirheumatic drugs) to ensure far wider distribution of benefits. Optimistically, new developments in technology and bio-engineering might dramatically reduce costs of present 'biological' therapies. (The antibiotics we now take for granted were once also horrendously expensive.). Pragmatically, one goal for this mission should include seriously pursuing more research and pilot clinical trials of non-protein combination therapies able to control: (i) TNF or other pro-inflammatory cytokines; and also (ii) other mediators sustaining chronic inflammation (-->pain, effusion, fibrosis, porosis, etc.). This can be immediately facilitated by drawing upon the immense resources of non-prescription Asia-Pacific traditional therapies--particularly when these have already been shown to either reduce TNF synthesis or control TNF-induced responses in preclinical studies. Could this be a major goal for the next decade, helping rectify some of the omissions of the current Bone & Joint Decade 2000-2010?

摘要

本文呼吁寻找(更好)的方法来扩大抗细胞因子疗法的效益,以确保它们尽可能广泛地应用。悲观地说,这可能涉及用更便宜的、虽然不太特异的非生物制剂来替代目前针对特定靶点的生物 DMARD(改善病情抗风湿药),以确保更广泛地分配效益。乐观地说,技术和生物工程的新发展可能会显著降低目前“生物”疗法的成本。(我们现在认为理所当然的抗生素曾经也是非常昂贵的。)。务实的做法是,这项任务的一个目标应该包括认真研究和进行更多的非蛋白联合治疗的试验,这些治疗能够控制:(i)TNF 或其他促炎细胞因子;以及(ii)维持慢性炎症的其他介质(-->疼痛、渗出、纤维化、骨质疏松症等)。这可以通过利用亚太地区非处方传统疗法的巨大资源来立即实现,特别是当这些疗法已经在临床前研究中被证明可以减少 TNF 的合成或控制 TNF 诱导的反应时。这是否可以成为下一个十年的一个主要目标,有助于纠正当前 2000-2010 年骨骼与关节十年计划的一些遗漏?

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