Lukacher A E, Morrison L A, Braciale V L, Malissen B, Braciale T J
J Exp Med. 1985 Jul 1;162(1):171-87. doi: 10.1084/jem.162.1.171.
Among murine class II major histocompatibility complex (MHC)-restricted cytotoxic T lymphocyte (CTL) clones specific for type A influenza virus, we have identified both noncytolytic clones and clones exhibiting H-2 I region-restricted cytolytic activity. After appropriate antigenic stimulation, both cytolytic and noncytolytic clones proliferated in the absence of exogenous interleukin 2. All of the clones possess the Thy-1.2+, Lyt-1+2-, L3T4+ phenotype. The class II MHC restriction of viral recognition by the CTL clones was mapped by proliferation using recombinant mouse strains and by inhibition of cytotoxic activity with monoclonal antibodies directed to class II MHC products and L3T4a. The restriction specificity of two CTL clones was unambiguously assigned to the E beta d chain by using L cell transfectant lines expressing E alpha kE beta d or E alpha kE beta k gene products. Analysis of the viral specificity of the cloned lines revealed subtype-specific and crossreactive patterns of viral antigen recognition; the pattern of viral antigen specificity exhibited by each clone in proliferation and cell-mediated cytotoxicity was identical. Each CTL clone also demonstrated antigen-dependent release of helper factor(s) that promoted in vitro primary anti-SRBC responses. Finally, the cytotoxic effector function of the class II MHC-restricted CTL clones was mediated by direct lysis of virus-infected cells, and not by secretion of a cytolytic lymphokine.
在针对甲型流感病毒的小鼠II类主要组织相容性复合体(MHC)限制性细胞毒性T淋巴细胞(CTL)克隆中,我们鉴定出了非细胞溶解克隆和表现出H-2 I区限制性细胞溶解活性的克隆。经过适当的抗原刺激后,细胞溶解克隆和非细胞溶解克隆在没有外源性白细胞介素2的情况下都能增殖。所有克隆都具有Thy-1.2 +、Lyt-1 + 2 -、L3T4 +表型。通过使用重组小鼠品系进行增殖以及用针对II类MHC产物和L3T4a的单克隆抗体抑制细胞毒性活性,来确定CTL克隆对病毒识别的II类MHC限制性。通过使用表达EαkEβd或EαkEβk基因产物的L细胞转染细胞系,将两个CTL克隆的限制性特异性明确地定位到Eβd链上。对克隆系的病毒特异性分析揭示了病毒抗原识别的亚型特异性和交叉反应模式;每个克隆在增殖和细胞介导的细胞毒性中表现出的病毒抗原特异性模式是相同的。每个CTL克隆还显示出抗原依赖性辅助因子的释放,这些因子促进了体外原发性抗SRBC反应。最后,II类MHC限制性CTL克隆的细胞毒性效应功能是通过直接裂解病毒感染细胞来介导的,而不是通过分泌细胞溶解淋巴因子。