Brunet J F, Denizot F, Golstein P
Centre d'Immunologie INSERM-CNRS de Marseille-Luminy, France.
Immunol Rev. 1988 Mar;103:21-36. doi: 10.1111/j.1600-065x.1988.tb00747.x.
One approach to the isolation of molecules involved in T cell-mediated cytolysis stems from the postulate of a possible correlation between molecular phenotype and molecular functional involvement. Accordingly, CTL-specific molecules have been looked for, using a strategy based on the differential screening of a subtracted cDNA library. This led to the isolation and characterization of the following structures, expressed mostly (but no exclusively) in CTLs and inducible upon lymphocyte activation: CTLA-1 and CTLA-3 (serine-proteases), CTLA-4 (a member of the Ig superfamily) and CTLA-2 alpha and beta (homologues to the proregion of cysteine-proteases). The theoretical and practical limitations and the prospects of this type of approach are discussed.
一种用于分离参与T细胞介导的细胞溶解的分子的方法,源于分子表型与分子功能参与之间可能存在相关性的假设。因此,利用基于对消减cDNA文库进行差异筛选的策略来寻找CTL特异性分子。这导致了以下结构的分离和表征,这些结构主要(但并非唯一)在CTL中表达,并在淋巴细胞激活后可诱导表达:CTLA-1和CTLA-3(丝氨酸蛋白酶)、CTLA-4(免疫球蛋白超家族成员)以及CTLA-2α和β(半胱氨酸蛋白酶原区的同源物)。本文讨论了这种方法的理论和实际局限性以及前景。