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趋化因子受体:多层面的治疗靶点。

Chemokine receptors: multifaceted therapeutic targets.

作者信息

Proudfoot Amanda E I

机构信息

Serono Pharmaceutical Research Institute, 14 chemin des Aulx, 1228 Plan les Ouates, Geneva, Switzerland.

出版信息

Nat Rev Immunol. 2002 Feb;2(2):106-15. doi: 10.1038/nri722.

DOI:10.1038/nri722
PMID:11910892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7097668/
Abstract

Chemokines and their receptors are involved in the pathogenesis of diseases ranging from asthma to AIDS. Chemokine receptors are G-protein-coupled serpentine receptors that present attractive tractable targets for the pharmaceutical industry. It is only ten years since the first chemokine receptor was discovered, and the rapidly expanding number of antagonists holds promise for new medicines to combat diseases that are currently incurable. Here, I focus on the rationale for developing antagonists of chemokine receptors for inflammatory disorders and AIDS, and the accumulating evidence that favours this strategy despite the apparent redundancy in the chemokine system.

摘要

趋化因子及其受体参与了从哮喘到艾滋病等多种疾病的发病过程。趋化因子受体是G蛋白偶联的蛇形受体,是制药行业颇具吸引力的可处理靶点。自首个趋化因子受体被发现至今仅十年,拮抗剂数量的迅速增加为研发对抗目前无法治愈疾病的新药带来了希望。在此,我重点探讨开发趋化因子受体拮抗剂用于治疗炎症性疾病和艾滋病的基本原理,以及尽管趋化因子系统存在明显冗余,但支持这一策略的证据却不断增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684e/7097668/0cbbf6edeb98/41577_2002_Article_BFnri722_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684e/7097668/42990c0ff5be/41577_2002_Article_BFnri722_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684e/7097668/6745a3432b2a/41577_2002_Article_BFnri722_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684e/7097668/c0dc4c6cfdee/41577_2002_Article_BFnri722_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684e/7097668/0cbbf6edeb98/41577_2002_Article_BFnri722_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684e/7097668/42990c0ff5be/41577_2002_Article_BFnri722_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684e/7097668/6745a3432b2a/41577_2002_Article_BFnri722_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684e/7097668/c0dc4c6cfdee/41577_2002_Article_BFnri722_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684e/7097668/0cbbf6edeb98/41577_2002_Article_BFnri722_Fig4_HTML.jpg

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Regulation of dendritic cell recruitment into resting and inflamed airway epithelium: use of alternative chemokine receptors as a function of inducing stimulus.
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Genetically encoded biosensor for monitoring spatiotemporal dynamics of CCR2 ligands in culture and in vivo.用于监测培养物和体内CCR2配体时空动态的基因编码生物传感器。
Nat Methods. 2025 Jul 15. doi: 10.1038/s41592-025-02742-y.
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