脊髓损伤后神经病理性疼痛中 M2 巨噬细胞的参与及其意义:系统综述

Aidin Shahrezaei, Maryam Sohani, Mohammadhassan Sohouli, Soroush Taherkhani, Farinaz Nasirinezhad
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摘要

神经病理性疼痛(NeP)是一种由神经系统疾病或损伤引发的持续性疼痛。虽然人们对 NeP 的基本病理生理机制知之甚少,但免疫系统在这种病症中发挥着关键作用。M2 巨噬细胞在组织愈合和减少炎症中起着关键作用。本系统性研究旨在概述 M2 巨噬细胞在脊髓损伤(SCI)后 NeP 中的作用和重要性。我们利用 Scopus、PubMed、Embase 和 ISI Web of Science 数据库进行了全面的系统性综述。两名独立审稿人对文章进行了筛选。所有出版物都研究了脊髓损伤后 M2 巨噬细胞对 NeP 的影响。对预先确定的偏倚实体进行了质量评估。11篇论文符合标准。研究结果表明,关注免疫细胞极化为治疗脊髓损伤后NeP和促进康复提供了可行的治疗方案。M2 巨噬细胞对减轻神经病理性疼痛和促进脊髓损伤后的恢复至关重要。伊维菌素功能化 MWCNTs、异鼠李素、Neuregulin-1 给药、TMEM16F 抑制、慢病毒介导的抗炎细胞因子递送、表儿茶素-3-棓酸盐和红光疗法等多种治疗方法对 M2 巨噬细胞的调节可促进神经再生、减少神经炎症细胞因子并减轻 NeP。不过,根据对纳入研究的质量评估和偏倚风险分析,必须谨慎解读这些临床前研究的结果。靶向 M2 巨噬细胞可能会带来治疗上的益处,因为它们对于治疗 NeP 和脊髓损伤后的恢复至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The involvement and significance of M2 macrophages in neuropathic pain following spinal cord injury: a systematic review
Neuropathic pain (NeP) is a type of persistent pain initiated by diseases or injuries of the nervous system. Although the underlying pathophysiological mechanisms of NeP are poorly understood, the immune system plays a key role in this condition. M2 macrophages have a key role in tissue healing and the reduction of inflammation. This systematic study aims to provide an overview of the role and importance of M2 macrophages in NeP after spinal cord injury (SCI). A comprehensive systematic review was conducted utilizing Scopus, PubMed, Embase, and ISI Web of Science databases. Two independent reviewers conducted the article selection. All publications examine the impact of M2 macrophages on NeP following spinal cord injuries. A quality assessment was conducted on bias entities that had been predetermined. Eleven papers met the criteria. According to the findings, focusing on immune cell polarization presents viable therapeutic options for treating NeP and enhancing recovery after SCI. M2 macrophages are essential for reducing neuropathic pain and promoting recovery after spinal cord injury. The modulation of M2 macrophages by a number of therapeutic approaches, including ivermectin-functionalized MWCNTs, isorhamnetin, Neuregulin-1 administration, TMEM16F inhibition, lentivirus-mediated delivery of anti-inflammatory cytokines, epigallocatechin-3-gallate, and red-light therapy promotes neuroregeneration, decreases neuroinflammatory cytokines, and reduces NeP. The results of these preclinical investigations must, however, be interpreted with caution, according to the quality assessment and risk of bias analysis of the studies that were included. Targeting M2 macrophages may have therapeutic benefits as they are essential for the management of NeP and recovery following spinal cord damage.
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