Gu Lijuan, Jian Zhihong, Stary Creed, Xiong Xiaoxing
Central Laboratory, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei, China.
Neurochem Res. 2015 Sep;40(9):1786-91. doi: 10.1007/s11064-015-1676-0. Epub 2015 Jul 29.
Stroke results in cerebral inflammation that causes brain injury and triggers immunodepression, resulting in an increased incidence of morbidity and mortality secondary to remote infection. It is well known that T cells modulate brain inflammation after ischemic stroke, and targeting T cells may be an innovative therapeutic strategy for stroke treatment. T cell deficiency is neuro-protective, but the observed protective effects differ between ischemic models. Recent studies suggest different T cell subsets may have distinct effects on the injured brain. In addition to their role in cerebral inflammation, T cells also play a role in stroke-induced immunodepression. Therefore, T cell-targeted therapies designed to provide protection against brain inflammation might paradoxically contribute to remote organ infection and mortality. Further investigations are required to determine the role of specific T cell subsets in cerebral inflammation and stroke-induced immunodepression, the optimal therapeutic window for treatment, and the appropriate dose of anti-T cell therapy.
中风会导致脑部炎症,进而引起脑损伤并引发免疫抑制,导致继发于远处感染的发病率和死亡率增加。众所周知,T细胞在缺血性中风后调节脑部炎症,靶向T细胞可能是中风治疗的一种创新治疗策略。T细胞缺陷具有神经保护作用,但在缺血模型中观察到的保护作用有所不同。最近的研究表明,不同的T细胞亚群可能对受损大脑有不同的影响。除了在脑部炎症中的作用外,T细胞在中风诱导的免疫抑制中也起作用。因此,旨在预防脑部炎症的靶向T细胞疗法可能会反常地导致远处器官感染和死亡。需要进一步研究以确定特定T细胞亚群在脑部炎症和中风诱导的免疫抑制中的作用、治疗的最佳时间窗以及抗T细胞疗法的合适剂量。