Takayama H, Shinohara N, Kawasaki A, Someya Y, Hanaoka S, Kojima H, Yagita H, Okumura K, Shinkai Y
Laboratory of Cellular Immunology, Mitsubishi Kasei Institute of Life Sciences, Tokyo, Japan.
Int Immunol. 1991 Nov;3(11):1149-56. doi: 10.1093/intimm/3.11.1149.
Despite a number of reports indicating that perforin, a pore-forming protein, is the primary effector molecule mediating specific target cell lysis by cytotoxic T lymphocytes (CTL), several lines of evidence suggest the existence of perforin-independent mechanisms. We established class II-restricted, soluble protein-specific CD4+ T cell clones with killing function which do not express a detectable amount of perforin and perforin mRNA. Nevertheless, these clones induced cytolysis and DNA fragmentation of target cells in a specific and highly directional manner which was not inhibitable by antibody against TNF/lymphotoxin. These data not only indicate the existence of cytotoxic T cell subsets which do not utilize perforin, but also suggest that perforin is not mandatory for specific target lysis by T cells.
尽管有许多报告表明,穿孔素(一种形成孔道的蛋白质)是介导细胞毒性T淋巴细胞(CTL)特异性杀伤靶细胞的主要效应分子,但有几条证据表明存在不依赖穿孔素的机制。我们建立了具有杀伤功能的II类限制性、可溶性蛋白特异性CD4 + T细胞克隆,这些克隆不表达可检测量的穿孔素和穿孔素mRNA。然而,这些克隆以一种特异性且高度定向的方式诱导靶细胞的细胞溶解和DNA片段化,而这种方式不受抗TNF/淋巴毒素抗体的抑制。这些数据不仅表明存在不利用穿孔素的细胞毒性T细胞亚群,还表明穿孔素对于T细胞特异性杀伤靶细胞并非必不可少。