Ptak W, Rózycka D, Rewicka M
Immunobiology. 1980 Jan;156(4-5):400-9. doi: 10.1016/S0171-2985(80)80073-8.
Injection of TNP-, DNP- or oxazolone-substituted syngeneic cells into mice causes the development of hapten-specific T suppressor cells which prevent the animals from being activity sensitized with homologous hapten. These cells injected together with immunized cells abrogate the latter's ability to transfer passively the contact sensitivity (CS) reaction into normal recipients. T lymphocytes from animals made unresponsive and sensitized with homologous hapten synthesize in vitro antigen-specific suppressor factors (SF) which when incubated with immune lymphocytes prevent them transferring adoptively the CS reaction. The type of cell used to induce suppression or production of suppressor factor (haptenated erythrocytes, thymocytes or macrophages) is not critical suggesting that a hapten-substituted common membrane structure is recognized as a tolerogen. The present work demonstrates that while the specific unresponsiveness induced by cell-bound hapten in vivo is long lasting, cells from tolerized animals are able to suppress the immunized cells in passive transfer or produce in vitro antigen-specific suppressor factors only when tested several days after tolerization.
将三硝基苯(TNP)、二硝基苯(DNP)或恶唑酮取代的同基因细胞注射到小鼠体内,会导致半抗原特异性T抑制细胞的发育,这些细胞可阻止动物被同源半抗原活性致敏。将这些细胞与免疫细胞一起注射,会消除后者将接触敏感性(CS)反应被动转移到正常受体中的能力。用同源半抗原使动物产生无反应性并致敏后,其T淋巴细胞在体外合成抗原特异性抑制因子(SF),该抑制因子与免疫淋巴细胞一起孵育时,会阻止它们将CS反应过继转移。用于诱导抑制或产生抑制因子的细胞类型(半抗原化红细胞、胸腺细胞或巨噬细胞)并不关键,这表明半抗原取代的共同膜结构被识别为耐受原。目前的研究表明,虽然体内细胞结合半抗原诱导的特异性无反应性持续时间长,但只有在耐受几天后进行检测时,来自耐受动物的细胞才能在被动转移中抑制免疫细胞或在体外产生抗原特异性抑制因子。