Finberg R, Burakoff S J, Benacerraf B, Greene M I
J Immunol. 1979 Sep;123(3):1210-4.
The subcutaneous administration of trinitrophenyl (TNP)-coupled syngeneic cells 7 days before co-culture with TNP-coupled syngeneic stimulator cells results in increased cytolytic activity. This augmented cytotoxic response has been shown to be dependent, at least partially, on radioresistant "helper" T cells. In this paper we have demonstrated that TNBS-generated suppressor T cells that are capable of suppressing contact sensitivity can specifically suppress the augmented response seen after subcutaneous priming. The i.v. administration of TNP-coupled cells results in priming of the recipient; however, if cells from these animals are transferred to a second recipient, there is evidence of suppressor activity. Thus, the cytotoxic T lymphocyte response is controlled by the same type of complex interactions previously demonstrated for humoral and delayed-type hypersensitivity responses.
在与三硝基苯基(TNP)偶联的同基因刺激细胞共培养前7天皮下注射TNP偶联的同基因细胞,可导致细胞溶解活性增强。这种增强的细胞毒性反应已被证明至少部分依赖于放射抗性的“辅助”T细胞。在本文中,我们证明了能够抑制接触敏感性的三硝基苯磺酸(TNBS)诱导的抑制性T细胞可以特异性抑制皮下致敏后出现的增强反应。静脉注射TNP偶联的细胞会使受体致敏;然而,如果将这些动物的细胞转移到第二个受体,就有抑制活性的证据。因此,细胞毒性T淋巴细胞反应受先前在体液和迟发型超敏反应中证明的相同类型的复杂相互作用控制。