Passmore J S, Glashoff R H, Lukey P T, Ress S R
Clinical Immunology Laboratory, Department of Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Clin Exp Immunol. 2001 Oct;126(1):76-83. doi: 10.1046/j.1365-2249.2001.01631.x.
One of the most important effector functions of activated gammadelta+ T cells in tuberculosis is their strong cytolytic activity against a variety of target cells, including M. tuberculosis-infected macrophages. In the present study, we investigated the relationship between the mechanism of cytolysis utilized by gammadelta+ CTL and intracellular M. tuberculosis survival using a panel of cytolytic human M. tuberculosis-specific gammadelta+ CTL clones. Cytolysis mediated by the gammadelta+ T-cell clones was found to be Ca2+-dependent, sensitive to Cyclosporin A, and was completely abrogated following Sr2+-induced de-granulation of the gammadelta+ T cell effectors. These data demonstrate that gammadelta+ T-cell-mediated cytoxicity was mediated via the granule exocytosis/perforin pathway. Despite significant cytolytic activity against mycobacteria infected U937 cells, the gammadelta+ CTL clones had no impact on the survival of intracellular M. tuberculosis.
活化的γδ+ T细胞在结核病中最重要的效应功能之一是它们对包括结核分枝杆菌感染的巨噬细胞在内的多种靶细胞具有强大的细胞溶解活性。在本研究中,我们使用一组细胞溶解的人结核分枝杆菌特异性γδ+ CTL克隆,研究了γδ+ CTL利用的细胞溶解机制与细胞内结核分枝杆菌存活之间的关系。发现γδ+ T细胞克隆介导的细胞溶解是Ca2+依赖性的,对环孢素A敏感,并且在Sr2+诱导γδ+ T细胞效应器脱颗粒后完全消除。这些数据表明,γδ+ T细胞介导的细胞毒性是通过颗粒胞吐/穿孔素途径介导的。尽管对感染分枝杆菌的U937细胞具有显著的细胞溶解活性,但γδ+ CTL克隆对细胞内结核分枝杆菌的存活没有影响。