Zheng Hong, Matte-Martone Catherine, Li Hongmei, Anderson Britt E, Venketesan Srividhya, Sheng Tan Hung, Jain Dhanpat, McNiff Jennifer, Shlomchik Warren D
Penn State Milton S. Hershey Medical Center, Department of Medicine, Hershey, PA, USA.
Blood. 2008 Feb 15;111(4):2476-84. doi: 10.1182/blood-2007-08-109678. Epub 2007 Nov 28.
Much of the efficacy of allogeneic hematopoietic stem cell transplantation (alloSCT) in curing hematologic malignancies is due to a graft-versus-leukemia (GVL) effect mediated by donor T cells that recognize recipient alloantigens on leukemic cells. Donor T cells are also important for reconstituting immunity in the recipient. Unfortunately, donor T cells can attack nonmalignant host tissues and cause graft-versus-host disease (GVHD). We previously reported that donor CD4(+) effector memory T cells (T(EMs)) do not cause GVHD but transfer functional T-cell memory. In the present work, we demonstrate in an MHC-mismatched model that CD4(+) T(EMs) (unprimed to recipient antigens) mediate GVL against clinically relevant mouse models of chronic phase and blast crisis chronic myelogenous leukemia, without causing GVHD. By creating gene-deficient leukemias and using perforin-deficient T cells, we demonstrate that direct cytolytic function is essential for T(EM)-mediated GVL, but that GVL is retained when killing via FasL, TNF-alpha, TRAIL, and perforin is individually impaired. However, T(EM)-mediated GVL was diminished when both FasL and perforin pathways were blocked. Taken together, our studies identify T(EMs) as a clinically applicable cell therapy for promoting GVL and immune reconstitution, particularly in MHC-mismatched haploidentical alloSCTs in which T cell-depleted allografts are commonly used to minimize GVHD.
同种异体造血干细胞移植(alloSCT)在治愈血液系统恶性肿瘤方面的大部分疗效归因于供体T细胞介导的移植物抗白血病(GVL)效应,这些供体T细胞可识别白血病细胞上的受体同种异体抗原。供体T细胞对于重建受体的免疫力也很重要。不幸的是,供体T细胞会攻击非恶性宿主组织并导致移植物抗宿主病(GVHD)。我们之前报道过,供体CD4(+)效应记忆T细胞(T(EMs))不会引发GVHD,但会传递功能性T细胞记忆。在本研究中,我们在MHC不匹配模型中证明,CD4(+) T(EMs)(未接触过受体抗原)介导针对慢性期和急变期慢性粒细胞白血病临床相关小鼠模型的GVL,而不会引发GVHD。通过构建基因缺陷型白血病并使用穿孔素缺陷型T细胞,我们证明直接细胞溶解功能对于T(EM)介导的GVL至关重要,但当通过FasL、TNF-α、TRAIL和穿孔素的杀伤作用单独受损时,GVL仍然存在。然而,当FasL和穿孔素途径均被阻断时,T(EM)介导的GVL会减弱。综上所述,我们的研究确定T(EMs)是一种临床适用的细胞疗法,可促进GVL和免疫重建,特别是在MHC不匹配的单倍体相合alloSCT中,其中通常使用去除T细胞的同种异体移植物来尽量减少GVHD。