Department of Immunology, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States.
Department of Microbiology and Immunology, Marlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland, Baltimore, MD, United States.
Front Immunol. 2018 Dec 19;9:2979. doi: 10.3389/fimmu.2018.02979. eCollection 2018.
Allogeneic hematopoietic cell transplantation (allo-HCT) is a potentially curative treatment for hematologic malignancies, and other hematologic and immunologic diseases. Donor-derived immune cells identify and attack cancer cells in the patient producing a unique graft-vs.-tumor (GVT) effect. This beneficial response renders allo-HCT one of the most effective forms of tumor immunotherapy. However, alloreactive donor T cells can damage normal host cells thereby causing graft-vs.-host disease (GVHD), which results in substantial morbidity and mortality. To date, GVHD remains as the major obstacle for more successful application of allo-HCT. Of special significance in this context are a number of cytotoxic pathways that are involved in GVHD and GVT response as well as donor cell engraftment. In this review, we summarize progress in the investigation of these cytotoxic pathways, including Fas/Fas ligand (FasL), perforin/granzyme, and cytokine pathways. Many studies have delineated their distinct operating mechanisms and how they are involved in the complex cellular interactions amongst donor, host, tumor, and infectious pathogens. Driven by progressing elucidation of their contributions in immune reconstitution and regulation, various interventional strategies targeting these pathways have entered translational stages with aims to improve the effectiveness of allo-HCT.
异基因造血细胞移植(allo-HCT)是治疗血液系统恶性肿瘤和其他血液及免疫性疾病的一种潜在治愈方法。供体来源的免疫细胞识别并攻击患者体内的癌细胞,产生独特的移植物抗肿瘤(GVT)效应。这种有益的反应使 allo-HCT 成为最有效的肿瘤免疫治疗形式之一。然而,同种反应性供体细胞可损伤正常宿主细胞,从而导致移植物抗宿主病(GVHD),这会导致大量发病率和死亡率。迄今为止,GVHD 仍然是 allo-HCT 更成功应用的主要障碍。在这方面特别重要的是一些细胞毒性途径,它们参与 GVHD 和 GVT 反应以及供体细胞植入。在这篇综述中,我们总结了对这些细胞毒性途径的研究进展,包括 Fas/Fas 配体(FasL)、穿孔素/颗粒酶和细胞因子途径。许多研究阐明了它们的独特作用机制,以及它们如何参与供体、宿主、肿瘤和感染病原体之间的复杂细胞相互作用。受其在免疫重建和调节中的作用不断阐明的推动,针对这些途径的各种干预策略已进入转化阶段,旨在提高 allo-HCT 的效果。