Maeda Yoshinobu, Levy Robert B, Reddy Pavan, Liu Chen, Clouthier Shawn G, Teshima Takanori, Ferrara James L M
Department of Internal Medicine, University of Michigan Comprehensive Cancer Center, 1500 East Medical Center Dr, Ann Arbor, MI 48109-0942, USA.
Blood. 2005 Mar 1;105(5):2023-7. doi: 10.1182/blood-2004-08-3036. Epub 2004 Oct 5.
Fas ligand (FasL) and perforin pathways not only are the major mechanisms of T cell-mediated cytotoxicity but also are involved in homeostatic regulation of these T cells. In the present study, we tested whether CD8+ donor T cells that are deficient in both perforin and FasL (cytotoxic double deficient [cdd]) could induce graft-versus-host disease (GVHD) in a major histocompatibility complex class I-mismatched lethally irradiated murine model. Interestingly, recipients of cdd CD8+ T cells demonstrated significantly greater serum levels of interferon gamma and tumor necrosis factor alpha and histopathologic damage from GVHD than wild-type (wt) T cells on day 30 after allogeneic bone marrow transplantation (P<.05). Wt and either perforin-deficient or FasL-deficient CD8+ T cells expanded early after transplantation followed by a contraction phase in which the majority of expanded CD8+ T cells were eliminated. In contrast, cdd CD8+ T cells exhibited prolonged expansion and reduced apoptosis to alloantigen stimulation in vivo and in vitro. Together these results suggest that donor cdd CD8+ T cells expand continuously and cause lethal GVHD, and that both perforin and FasL are required for the contraction of allo-reactive CD8+ T cells.
Fas配体(FasL)和穿孔素途径不仅是T细胞介导的细胞毒性的主要机制,还参与这些T细胞的稳态调节。在本研究中,我们测试了在主要组织相容性复合体I类不匹配的致死性照射小鼠模型中,穿孔素和FasL均缺陷的CD8⁺供体T细胞(细胞毒性双缺陷[cdd])是否能诱导移植物抗宿主病(GVHD)。有趣的是,在异基因骨髓移植后第30天,cdd CD8⁺ T细胞受体的血清干扰素γ和肿瘤坏死因子α水平显著高于野生型(wt)T细胞,且GVHD导致的组织病理学损伤更严重(P<0.05)。wt以及穿孔素缺陷或FasL缺陷的CD8⁺ T细胞在移植后早期扩增,随后进入收缩期,在此期间大多数扩增的CD8⁺ T细胞被清除。相比之下,cdd CD8⁺ T细胞在体内和体外对同种异体抗原刺激均表现出延长的扩增和减少的凋亡。这些结果共同表明,供体cdd CD8⁺ T细胞持续扩增并导致致死性GVHD,且穿孔素和FasL对于同种反应性CD8⁺ T细胞的收缩都是必需的。