Zhang Zhi-Ming, Shi Rongchen, Chen Hong, Zhang Zhiren
Department of Medicine, Shunde Polytechnic, Desheng East Street, Foshan, 528300, China.
Institute of Immunology, Third Military Medical University of PLA, Gaotanyan Street 30, Chongqing, 400038, China.
Neurol Sci. 2016 Feb;37(2):199-203. doi: 10.1007/s10072-015-2384-x. Epub 2015 Sep 26.
Experimental autoimmune neuritis (EAN) is a well-known animal model of human demyelinating polyneuropathies. Macrophages are the major immune cells in peripheral nerves and may exert tissue-damage or tissue-protective activity during EAN. While considered to define a subpopulation of T lymphocytes, CD8 expression has been found on certain macrophages that show cytotoxic effects. Here we have studied the spatiotemporal accumulation of CD8(+) cells in sciatic nerves of EAN rats. A robust accumulation of CD8(+) cells was observed in the sciatic nerves of EAN rats, which was positively correlated with the severity of neurological signs in EAN. Moreover, double-labelling experiments showed that the major cellular sources of CD8 were reactive macrophages. Therefore, our data here suggest a pathological role of CD8(+) macrophages in EAN, which makes CD8(+) macrophage a potential therapeutic target for EAN.
实验性自身免疫性神经炎(EAN)是一种众所周知的人类脱髓鞘性多发性神经病动物模型。巨噬细胞是周围神经中的主要免疫细胞,在EAN过程中可能发挥组织损伤或组织保护活性。虽然CD8表达被认为是T淋巴细胞亚群的定义,但在某些具有细胞毒性作用的巨噬细胞上也发现了CD8表达。在此,我们研究了EAN大鼠坐骨神经中CD8(+)细胞的时空积累情况。在EAN大鼠的坐骨神经中观察到CD8(+)细胞的大量积累,这与EAN中神经学体征的严重程度呈正相关。此外,双标记实验表明CD8的主要细胞来源是反应性巨噬细胞。因此,我们的数据表明CD8(+)巨噬细胞在EAN中具有病理作用,这使得CD8(+)巨噬细胞成为EAN的潜在治疗靶点。