Calder V L, Zhao Z S, Wang Y, Barton K, Lightman S L
Dept. of Clinical Science, Institute of Ophthalmology, London, U.K.
Immunology. 1993 Jun;79(2):255-62.
During the later stages of soluble-antigen (sAg)-induced experimental autoimmune uveoretinitis (EAU), an increase in the relative number of CD8+ lymphocytes has been observed at the site of inflammation in the retina. It has been suggested that these late-appearing CD8+ cells might down-regulate this acute disease process. To determine the role of the CD8+ cells in EAU, Lewis rats were depleted of CD8+ cells prior to and during disease and the enucleated eyes examined histologically. The spleen cells from CD8-depleted rats were also examined for their ability to respond to concanavalin A (Con A) and to allogeneic targets as determined by mixed lymphocyte reaction (MLR) and cytotoxicity assays. The results suggest that depleting CD8+ cells had no effect on the course of disease and that CD8+ cells do not play a crucial role in the immunoregulation of EAU.
在可溶性抗原(sAg)诱导的实验性自身免疫性葡萄膜视网膜炎(EAU)后期,视网膜炎症部位的CD8 +淋巴细胞相对数量有所增加。有人认为,这些后期出现的CD8 +细胞可能会下调这种急性疾病进程。为了确定CD8 +细胞在EAU中的作用,在疾病发生之前和期间,对Lewis大鼠进行CD8 +细胞清除,并对摘除的眼睛进行组织学检查。还通过混合淋巴细胞反应(MLR)和细胞毒性试验,检测了CD8缺失大鼠的脾细胞对刀豆球蛋白A(Con A)和异基因靶标的反应能力。结果表明,清除CD8 +细胞对疾病进程没有影响,并且CD8 +细胞在EAU的免疫调节中不发挥关键作用。