Barzaga-Gilbert M E, Skeen M J, Chou C H, Fritz R B
Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322.
J Neuroimmunol. 1989 Aug;23(3):241-7. doi: 10.1016/0165-5728(89)90056-8.
Myelin basic protein (MBP)-specific T cell lines derived from SJL mice lose the ability to transfer adoptively experimental allergic encephalomyelitis (EAE) after 5-6 restimulations with antigen in vitro. In order to test whether such lines were suppressive, non-encephalitogenic T cell lines were co-cultured with a freshly derived encephalitogenic T cell line. Following co-culture in the presence of MBP and irradiated syngeneic spleen cells the mixture was transferred adoptively to syngeneic recipients. Severe EAE was observed in recipients of the encephalitogenic cell line alone but not in animals which received the co-culture. A co-culture period was required as mixing the encephalitogenic and non-encephalitogenic T cell lines just prior to transfer was without effect. Not all non-encephalitogenic cell lines were found to be suppressive. Culture fluids from the suppressive, but not the non-suppressive lines were found to inhibit MBP-driven proliferation of T cell clones and encephalitogenic lines in vitro. Nineteen of 55 MBP-specific T cell clones derived from suppressive lines were found to elaborate the suppressive supernatant activity. The suppressive effect was not antigen-specific since the same culture supernatants inhibited proliferation of an ovalbumin-specific SJL T cell clone. The suppressive effect became apparent only after T cell lines had lost encephalitogenicity and was not mediated by tumor necrosis factor, lymphotoxin or prostaglandin.
从SJL小鼠获得的髓鞘碱性蛋白(MBP)特异性T细胞系,在体外经抗原再次刺激5 - 6次后,失去了过继转移实验性变应性脑脊髓炎(EAE)的能力。为了检测这类细胞系是否具有抑制作用,将非致脑炎性T细胞系与新获得的致脑炎性T细胞系共同培养。在MBP和经照射的同基因脾细胞存在的情况下进行共同培养后,将混合物过继转移给同基因受体。单独接种致脑炎性细胞系的受体出现了严重的EAE,而接种共同培养物的动物则未出现。需要一段共同培养期,因为在转移前将致脑炎性和非致脑炎性T细胞系混合则没有效果。并非所有非致脑炎性细胞系都具有抑制作用。发现来自具有抑制作用而非无抑制作用细胞系的培养液,在体外可抑制MBP驱动的T细胞克隆和致脑炎性细胞系的增殖。在来自具有抑制作用细胞系的55个MBP特异性T细胞克隆中,有19个被发现可产生具有抑制作用的上清液活性。这种抑制作用不是抗原特异性的,因为相同的培养上清液可抑制卵清蛋白特异性SJL T细胞克隆的增殖。这种抑制作用仅在T细胞系失去致脑炎性后才明显,且不是由肿瘤坏死因子、淋巴毒素或前列腺素介导的。