van den Brink Marcel R M, Burakoff Steven J
Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Nat Rev Immunol. 2002 Apr;2(4):273-81. doi: 10.1038/nri775.
The remarkable activity of donor T cells against malignant cells in the context of an allogeneic haematopoietic stem-cell transplantation (HSCT) is arguably, at present, the most potent clinical immunotherapy for cancer. However, alloreactive donor T cells are also important effector cells in the development of graft-versus-host disease (GVHD), which is a potentially lethal complication for recipients of an allogeneic HSCT. Therefore, the separation of the GVHD and graft-versus-tumour (GVT) activity of donor T cells has become a topic of great interest for many investigators. Recent studies have shown that donor T cells make differential use of their cytolytic pathways in mediating GVHD and GVT effects. Therefore, the selective blockade or enhancement of cytolytic pathways provides an intriguing therapeutic opportunity to separate the desired GVT effect from the potentially devastating GVHD.
在同种异体造血干细胞移植(HSCT)背景下,供体T细胞对恶性细胞具有显著活性,目前这可以说是最有效的癌症临床免疫疗法。然而,同种异体反应性供体T细胞也是移植物抗宿主病(GVHD)发生过程中的重要效应细胞,而GVHD是同种异体HSCT受者的一种潜在致命并发症。因此,分离供体T细胞的GVHD和移植物抗肿瘤(GVT)活性已成为许多研究人员极为感兴趣的话题。最近的研究表明,供体T细胞在介导GVHD和GVT效应时对其细胞溶解途径的利用存在差异。因此,选择性阻断或增强细胞溶解途径为将所需的GVT效应与潜在的破坏性GVHD分离提供了一个有趣的治疗机会。