Fisch P, Malkovsky M, Braakman E, Sturm E, Bolhuis R L, Prieve A, Sosman J A, Lam V A, Sondel P M
Department of Human Oncology, University of Wisconsin, Madison 53792.
J Exp Med. 1990 May 1;171(5):1567-79. doi: 10.1084/jem.171.5.1567.
Non-MHC-restricted killer cells are cytotoxic lymphocytes that can mediate cytolysis of most tumor targets without apparent selectivity and restriction by the MHC, particularly when activated with IL-2. These effector cells include predominantly NK cells and T cells expressing the TCR-gamma/delta. We found that TCR-gamma/delta-1+, delta TSC1-, BB3+, Ti gamma A+ T cell clones mediate a characteristic cytolytic pattern of non-MHC-restricted cytolysis that is markedly different from NK clones and alpha/beta T cell clones derived from the peripheral blood of the same normal individuals. The characteristic finding is that all BB3/Ti gamma A+ gamma/delta clones mediate strong cytolysis of Daudi cells but they do not lyse Raji cells. In contrast, NK clones from the same donors mediate strong cytolysis of both Daudi and Raji targets. Cytotoxicity by the gamma/delta clones on certain target cells such as Daudi and Molt 4 can be specifically inhibited by mAbs reactive against the TCR-gamma/delta. Therefore, the TCR-gamma/delta on these clones either directly recognizes target epitopes on some tumor targets or it is involved in the regulation of their cytotoxic function. The expression of TCR-gamma/delta products reacting with the BB3 and Ti gamma A mAbs reflects the usage of identical TCR-gamma/delta V region genes that appear to be associated with the characteristic pattern of non-MHC-restricted cytotoxicity displayed by this major subset of human peripheral blood gamma/delta cells.
非MHC限制杀伤细胞是细胞毒性淋巴细胞,能够介导对大多数肿瘤靶标的细胞溶解,且不受MHC明显的选择性和限制,尤其是在用白细胞介素-2激活时。这些效应细胞主要包括自然杀伤细胞(NK细胞)和表达TCR-γ/δ的T细胞。我们发现,TCR-γ/δ-1+、δTSC1-、BB3+、TiγA+ T细胞克隆介导一种非MHC限制细胞溶解的特征性细胞溶解模式,这与来自相同正常个体外周血的NK细胞克隆和α/β T细胞克隆明显不同。特征性发现是,所有BB3/TiγA+γ/δ克隆均介导对Daudi细胞的强烈细胞溶解,但它们不裂解Raji细胞。相反,来自相同供体的NK细胞克隆介导对Daudi和Raji靶标的强烈细胞溶解。γ/δ克隆对某些靶细胞(如Daudi和Molt 4)的细胞毒性可被针对TCR-γ/δ的单克隆抗体特异性抑制。因此,这些克隆上的TCR-γ/δ要么直接识别某些肿瘤靶标上的靶表位,要么参与其细胞毒性功能的调节。与BB3和TiγA单克隆抗体反应的TCR-γ/δ产物的表达反映了相同TCR-γ/δ V区基因的使用情况,这些基因似乎与人类外周血γ/δ细胞这一主要亚群所显示的非MHC限制细胞毒性的特征模式相关。