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靶向趋化因子配体 2-趋化因子受体 2 轴为慢性疼痛的免疫治疗提供了可能。

Targeting the chemokine ligand 2-chemokine receptor 2 axis provides the possibility of immunotherapy in chronic pain.

机构信息

Department of Pharmacology, School of Pharmacy, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750004, China.

Department of Pharmacology, School of Pharmacy, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750004, China; Ningxia Special Traditional Medicine Modern Engineering Research Center and Collaborative Innovation Center, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750004, China.

出版信息

Eur J Pharmacol. 2023 May 15;947:175646. doi: 10.1016/j.ejphar.2023.175646. Epub 2023 Mar 11.

Abstract

Chronic pain affects patients' physical and psychological health and quality of life, entailing a tremendous public health challenge. Currently, drugs for chronic pain are usually associated with a large number of side effects and poor efficacy. Chemokines in the neuroimmune interface combine with their receptors to regulate inflammation or mediate neuroinflammation in the peripheral and central nervous system. Targeting chemokines and their receptor-mediated neuroinflammation is an effective means to treat chronic pain. In recent years, growing evidence has shown that the expression of chemokine ligand 2 (CCL2) and its main chemokine receptor 2 (CCR2) is involved in its occurrence, development and maintenance of chronic pain. This paper summarises the relationship between the chemokine system, CCL2/CCR2 axis, and chronic pain, and the CCL2/CCR2 axis changes under different chronic pain conditions. Targeting chemokine CCL2 and its chemokine receptor CCR2 through siRNA, blocking antibodies, or small molecule antagonists may provide new therapeutic possibilities for managing chronic pain.

摘要

慢性疼痛影响患者的身心健康和生活质量,带来了巨大的公共卫生挑战。目前,治疗慢性疼痛的药物通常伴随着大量的副作用和较差的疗效。神经免疫界面中的趋化因子与它们的受体结合,调节外周和中枢神经系统的炎症或介导神经炎症。针对趋化因子及其受体介导的神经炎症是治疗慢性疼痛的有效手段。近年来,越来越多的证据表明,趋化因子配体 2 (CCL2)及其主要趋化因子受体 2 (CCR2)的表达参与了慢性疼痛的发生、发展和维持。本文总结了趋化因子系统、CCL2/CCR2 轴与慢性疼痛的关系,以及不同慢性疼痛条件下 CCL2/CCR2 轴的变化。通过 siRNA、阻断抗体或小分子拮抗剂靶向趋化因子 CCL2 和其趋化因子受体 CCR2 可能为管理慢性疼痛提供新的治疗可能性。

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