Westarp M E, Wekerle H, Ben-Nun A, Cohen I R, Vohl M L, Przuntek H
J Pharmacol Exp Ther. 1987 Aug;242(2):614-20.
An acute form of transferred experimental allergic encephalomyelitis was induced by injection of activated, myelin basic protein-specific T cell line lymphocytes. The course of the disease as a function of the dose of cytotoxic cells was investigated, and the effect of i.p. and i.v. application of methotrexate on mortality and morbidity was determined. Depending on the time of administration, beneficial therapeutic effects could be seen as early as 1 week. Survival of animals that had received a lethal dose of 15 to 20 X 10(6) cells/kg proved to be the most valuable parameter. T lymphocyte line-mediated experimental allergic encephalomyelitis is a predictable acute central nervous system model disease that does not require antigen depots or cell donor animals.
通过注射活化的、髓鞘碱性蛋白特异性T细胞系淋巴细胞诱导出急性形式的转移实验性过敏性脑脊髓炎。研究了疾病进程与细胞毒性细胞剂量的关系,并确定了腹腔注射和静脉注射甲氨蝶呤对死亡率和发病率的影响。根据给药时间,早在1周时就能观察到有益的治疗效果。接受15至20×10(6)个细胞/千克致死剂量的动物的存活情况被证明是最有价值的参数。T淋巴细胞系介导的实验性过敏性脑脊髓炎是一种可预测的急性中枢神经系统模型疾病,不需要抗原储存库或细胞供体动物。