作为免疫学新靶点的 CXCR4:摆脱典型拮抗剂的束缚。

Future drug discovery Pub Date : 2022-06-01 Epub Date: 2022-07-19 DOI:10.4155/fdd-2022-0007
Birgit Caspar, Pietro Cocchiara, Armelle Melet, Kristof Van Emelen, Annegret Van der Aa, Graeme Milligan, Jean-Philippe Herbeuval
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引用次数: 0

摘要

多年来,CXCR4 一直是药物发现领域关注的目标。然而,迄今为止,即使不是所有研究,也大多集中于寻找 CXCR4 功能的拮抗剂。最近的研究表明,以 CXCR4 的一个次要异构口袋为靶点,可诱导表达 CXCR4 的免疫细胞产生免疫调节效应,并与 TLR 途径相连。与这个小口袋结合的化合物似乎具有功能选择性,在选定的 GPCR 信号通路(Gi 激活)中具有反向激动特性,但免疫调节效应可能还涉及其他信号通路。对这些 CXCR4 靶向免疫调节剂的深入研究可能会为(自身)免疫性疾病带来新的治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

CXCR4 as a novel target in immunology: moving away from typical antagonists.

CXCR4 as a novel target in immunology: moving away from typical antagonists.

CXCR4 as a novel target in immunology: moving away from typical antagonists.

CXCR4 as a novel target in immunology: moving away from typical antagonists.

CXCR4 has been a target of interest in drug discovery for numerous years. However, so far, most if not all studies focused on finding antagonists of CXCR4 function. Recent studies demonstrate that targeting a minor allosteric pocket of CXCR4 induces an immunomodulating effect in immune cells expressing CXCR4, connected to the TLR pathway. Compounds binding in this minor pocket seem to be functionally selective with inverse agonistic properties in selected GPCR signaling pathways (Gi activation), but additional signaling pathways are likely to be involved in the immunomodulating effects. In depth research into these CXCR4-targeted immunomodulators could lead to novel treatment options for (auto)-immune diseases.

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