Babu U M, Sabbadini E
J Immunol. 1977 Aug;119(2):781-5.
Lethally irradiated F1 hybrid mice were given an i.v. injection of parental strain spleen cells. Six days later, their spleen cells were used as the effector cells to measure the in vitro cell-mediated cytotoxicity (CMC) of the parental cells. The treatment of the donors with hydrocortisone resulted in a marked decrease of the capacity of their spleen cells to produce a CMC reaction, whereas the treatment with antithymocyte serum (ATS) resulted in an almost complete loss of such activity. The mixing of spleen cells from hydrocortisone-treated parental donors with the spleen cells from ATS-treated parental donors before injection resulted in a synergistic amplification of the cytotoxic response. The anti-Thy-1 serum treatment of either spleen cell population abolished the synergism completely. These results indicate that cortico-resistant T cells act as precursors of cytotoxic lymphocytes and that ATS-resistant T cells produce an amplification of their reaction.
对受致死剂量照射的F1杂交小鼠进行静脉注射亲代品系脾细胞。六天后,将其脾细胞用作效应细胞,以测量亲代细胞的体外细胞介导细胞毒性(CMC)。用氢化可的松处理供体导致其脾细胞产生CMC反应的能力显著降低,而用抗胸腺细胞血清(ATS)处理则导致这种活性几乎完全丧失。在注射前,将来自氢化可的松处理的亲代供体的脾细胞与来自ATS处理的亲代供体的脾细胞混合,导致细胞毒性反应协同放大。对任一脾细胞群体进行抗Thy-1血清处理可完全消除这种协同作用。这些结果表明,皮质激素抗性T细胞作为细胞毒性淋巴细胞的前体,而ATS抗性T细胞可增强其反应。