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哮喘转化医学:成绩单。

Asthma translational medicine: report card.

机构信息

Profectus Pharma Consulting, Inc, San Jose, CA 95125, United States.

出版信息

Biochem Pharmacol. 2011 Sep 15;82(6):567-85. doi: 10.1016/j.bcp.2011.06.038. Epub 2011 Jul 2.

Abstract

Over the last 30 years, scientific research into asthma has focused almost exclusively on one component of the disorder - airway inflammation - as being the key underlying feature. These studies have provided a remarkably detailed and comprehensive picture of the events following antigen challenge that lead to an influx of T cells and eosinophils in the airways. Indeed, in basic research, even the term "asthma" has become synonymous with a T helper 2 cell-mediated disorder. From this cascade of cellular activation processes and mediators that have been identified it has been possible to pinpoint critical junctures for therapeutic intervention, leading experimentalists to produce therapies that are very effective in decreasing airway inflammation in animal models. Many of these compounds have now completed early Phase 2 "proof-of-concept" clinical trials so the translational success of the basic research model can be evaluated. This commentary discusses clinical results from 39 compounds and biologics acting at 23 different targets, and while 6 of these drugs can be regarded as a qualified success, none benefit the bulk of asthma sufferers. Despite this disappointing rate of success, the same immune paradigm and basic research models, with a few embellishments to incorporate newly identified cells and mediators, continue to drive target identification and drug discovery efforts. It is time to re-evaluate the focus of these efforts.

摘要

在过去的 30 年中,哮喘的科学研究几乎完全集中在该疾病的一个组成部分——气道炎症——作为关键的潜在特征。这些研究提供了一个非常详细和全面的描述,即在抗原挑战后导致 T 细胞和嗜酸性粒细胞流入气道的事件。事实上,在基础研究中,即使是“哮喘”这个术语也已经成为 T 辅助 2 细胞介导疾病的代名词。从已经确定的细胞激活过程和介质的级联中,可以确定治疗干预的关键节点,从而导致实验学家产生在动物模型中非常有效地减少气道炎症的疗法。其中许多化合物现在已经完成了早期的 2 期“概念验证”临床试验,因此可以评估基础研究模型的转化成功。本评论讨论了来自 39 种化合物和 23 种不同靶点的生物制剂的临床结果,尽管其中 6 种药物可以被视为合格的成功,但没有一种药物能使大多数哮喘患者受益。尽管成功率如此令人失望,但同样的免疫范例和基础研究模型,稍加改进,纳入新发现的细胞和介质,继续推动目标识别和药物发现的努力。现在是重新评估这些努力重点的时候了。

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