Wang Xiangzi, Niu Xiaofei, Wang Yingkai, Liu Yang, Yang Cheng, Chen Xuyi, Qi Zhongquan
School of Medicine, Guangxi University, Nanning, Guangxi Zhuang Autonomous Region, China.
Graduate School of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Neural Regen Res. 2025 Aug 1;20(8):2231-2244. doi: 10.4103/NRR.NRR-D-24-00119. Epub 2024 Jul 29.
Spinal cord injury involves non-reversible damage to the central nervous system that is characterized by limited regenerative capacity and secondary inflammatory damage. The expression of the C-C motif chemokine ligand 2/C-C motif chemokine receptor 2 axis exhibits significant differences before and after injury. Recent studies have revealed that the C-C motif chemokine ligand 2/C-C motif chemokine receptor 2 axis is closely associated with secondary inflammatory responses and the recruitment of immune cells following spinal cord injury, suggesting that this axis is a novel target and regulatory control point for treatment. This review comprehensively examines the therapeutic strategies targeting the C-C motif chemokine ligand 2/C-C motif chemokine receptor 2 axis, along with the regenerative and repair mechanisms linking the axis to spinal cord injury. Additionally, we summarize the upstream and downstream inflammatory signaling pathways associated with spinal cord injury and the C-C motif chemokine ligand 2/C-C motif chemokine receptor 2 axis. This review primarily elaborates on therapeutic strategies that target the C-C motif chemokine ligand 2/C-C motif chemokine receptor 2 axis and the latest progress of research on antagonistic drugs, along with the approaches used to exploit new therapeutic targets within the C-C motif chemokine ligand 2/C-C motif chemokine receptor 2 axis and the development of targeted drugs. Nevertheless, there are presently no clinical studies relating to spinal cord injury that are focusing on the C-C motif chemokine ligand 2/C-C motif chemokine receptor 2 axis. This review aims to provide new ideas and therapeutic strategies for the future treatment of spinal cord injury.
脊髓损伤涉及中枢神经系统的不可逆损伤,其特征为再生能力有限和继发性炎症损伤。C-C基序趋化因子配体2/C-C基序趋化因子受体2轴的表达在损伤前后表现出显著差异。最近的研究表明,C-C基序趋化因子配体2/C-C基序趋化因子受体2轴与脊髓损伤后的继发性炎症反应和免疫细胞募集密切相关,这表明该轴是一个新的治疗靶点和调控控制点。本综述全面研究了针对C-C基序趋化因子配体2/C-C基序趋化因子受体2轴的治疗策略,以及将该轴与脊髓损伤联系起来的再生和修复机制。此外,我们总结了与脊髓损伤以及C-C基序趋化因子配体2/C-C基序趋化因子受体2轴相关的上游和下游炎症信号通路。本综述主要阐述了针对C-C基序趋化因子配体2/C-C基序趋化因子受体2轴的治疗策略以及拮抗药物的最新研究进展,以及在C-C基序趋化因子配体2/C-C基序趋化因子受体2轴内开发新治疗靶点的方法和靶向药物的研发。然而,目前尚无专注于C-C基序趋化因子配体2/C-C基序趋化因子受体2轴的脊髓损伤临床研究。本综述旨在为未来脊髓损伤的治疗提供新思路和治疗策略。