Macphail S, Stutman O
Memorial Sloan-Kettering Cancer Center, Immunology Program, New York, NY 10021.
J Immunol. 1987 Dec 15;139(12):4007-15.
Thy-1+, L3T4+, Ly-2- cytotoxic lymphocytes (CTL) are generated in a primary anti-H-2d mixed lymphocyte reaction, by using responders depleted of Ly-2+ cells. In addition to expressing the L3T4 marker, as detected by anti-L3T4 antibody and complement-mediated elimination, the L3T4+ CTL are inhibited by L3T4 antibody. The observation of these L3T4+ CTL in cells recovered from primary mixed lymphocyte reactions confirms the previous reports. However it is demonstrated for the first time that a subpopulation of these are class I-specific by their specific inhibition with an antiserum to class I antigens. The class I specificity of the CTL was further shown by their ability to kill class II antigen negative P815 tumor cells. The lysis of this target cell by L3T4+ CTL was also specifically blocked by the class I antiserum. The data is consistent with the presence also of a class II-specific population of L3T4+ cytotoxic cells. The fact that a level of L3T4+ cell-mediated cytotoxic activity comparable to Ly-2+ cytolytic activity is generated in a primary mixed lymphocyte response, even though the precursor frequency of L3T4+ killer cells is 10 times lower than for Ly-2+ killers, is suggestive of their physiologic significance. It was also shown that the activation of these cells is not dependent on the presence of xenogeneic serum components or exogenous helper or mitogenic factors in the culture medium. The findings provide further evidence against both the phenotype-function and phenotype-major histocompatibility complex antigen specificity models of T cell diversity.
通过使用去除Ly-2+细胞的应答细胞,在原发性抗H-2d混合淋巴细胞反应中产生Thy-1+、L3T4+、Ly-2-细胞毒性淋巴细胞(CTL)。除了表达L3T4标志物(通过抗L3T4抗体检测及补体介导的清除)外,L3T4+ CTL还受到L3T4抗体的抑制。从原发性混合淋巴细胞反应中回收的细胞中观察到这些L3T4+ CTL,证实了先前的报道。然而,首次证明其中一个亚群通过用I类抗原抗血清进行特异性抑制而具有I类特异性。CTL的I类特异性还通过其杀伤II类抗原阴性P815肿瘤细胞的能力进一步显示。L3T4+ CTL对该靶细胞的裂解也被I类抗血清特异性阻断。数据表明也存在L3T4+细胞毒性细胞的II类特异性群体。尽管L3T4+杀伤细胞的前体频率比Ly-2+杀伤细胞低10倍,但在原发性混合淋巴细胞反应中产生的L3T4+细胞介导的细胞毒性活性水平与Ly-2+溶细胞活性相当,这暗示了它们的生理意义。还表明这些细胞的激活不依赖于培养基中异种血清成分或外源性辅助或促有丝分裂因子的存在。这些发现为反对T细胞多样性的表型-功能和表型-主要组织相容性复合体抗原特异性模型提供了进一步的证据。