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肿瘤坏死因子受体 2(TNFR2):一个新兴药物靶点概述。

Tumor necrosis factor receptor-2 (TNFR2): an overview of an emerging drug target.

机构信息

a Division for Molecular Internal Medicine, Department of Internal Medicine II , University Hospital Würzburg , Würzburg , Germany.

出版信息

Expert Opin Ther Targets. 2019 Apr;23(4):295-307. doi: 10.1080/14728222.2019.1586886. Epub 2019 Mar 19.

DOI:10.1080/14728222.2019.1586886
PMID:30856027
Abstract

Tumor necrosis factor (TNF) receptor 2 (TNFR2) is one of two receptors of the cytokines, TNF and lymphotoxin-α. TNFR1 is a strong inducer of proinflammatory activities. TNFR2 has proinflammatory effects too, but it also elicits strong anti-inflammatory activities and has protective effects on oligodendrocytes, cardiomyocytes, and keratinocytes. The protective and anti-inflammatory effects of TNFR2 may explain why TNF inhibitors failed to be effective in diseases such as heart failure or multiple sclerosis, where TNF has been strongly implicated as a driving force. Stimulatory and inhibitory TNFR2 targeting hence attracts considerable interest for the treatment of autoimmune diseases and cancer. Areas covered: Based on a brief description of the pathophysiological importance of the TNF-TNFR1/2 system, we discuss the potential applications of TNFR2 targeting therapies. We also debate TNFR2 activation as a way forward in the search for TNFR2-specific agents. Expert opinion: The use of TNFR2 to target regulatory T-cells is attractive, but this approach is just one amongst many suitable targets. With respect to its preference for Treg stimulation and protection of non-immune cells, TNFR2 is more unique and thus offers opportunities for translational success.

摘要

肿瘤坏死因子(TNF)受体 2(TNFR2)是细胞因子 TNF 和淋巴毒素-α的两种受体之一。TNFR1 是促炎活性的强诱导剂。TNFR2 也具有促炎作用,但它也会引发强烈的抗炎活性,并对少突胶质细胞、心肌细胞和角质细胞具有保护作用。TNFR2 的保护和抗炎作用可能解释了为什么 TNF 抑制剂在心力衰竭或多发性硬化等疾病中无效,而 TNF 被强烈认为是这些疾病的驱动力。因此,刺激和抑制 TNFR2 成为治疗自身免疫性疾病和癌症的研究热点。

涵盖领域

基于对 TNF-TNFR1/2 系统的病理生理学重要性的简要描述,我们讨论了 TNFR2 靶向治疗的潜在应用。我们还讨论了 TNFR2 激活作为寻找 TNFR2 特异性药物的一种方法。

专家意见

利用 TNFR2 靶向调节性 T 细胞具有吸引力,但这种方法只是众多合适靶点之一。鉴于其对 Treg 刺激和非免疫细胞保护的偏好,TNFR2 更加独特,因此为转化成功提供了机会。

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