Till Brian G, Press Oliver W
Research Associate, Acting Instructor, University of Washington, Fred Hutchinson Cancer Research Center, Department of Medicine, Seattle, WA 98109, USA.
Expert Opin Biol Ther. 2009 Nov;9(11):1407-25. doi: 10.1517/14712590903260785.
Chemotherapy-resistant lymphomas can be cured with allogeneic hematopoietic cell transplantation, demonstrating the susceptibility of these tumors to T cell mediated immune responses. However, high rates of transplant-related morbidity and mortality limit this approach. Efforts have, therefore, been made to develop alternative T cell based therapies, and there is growing evidence that adoptive therapy with T cells targeted to lymphoma-associated antigens may be a safe and effective new method for treating this group of diseases.
OBJECTIVE/METHODS: We review publications on adoptive therapy with ex vivo expanded T cells targeting viral antigens, as well as genetically modified autologous T cells, as strategies for the treatment of lymphoma, with the goal of providing an overview of these approaches.
RESULTS/CONCLUSIONS: Epstein-Barr virus specific T cell therapy is an effective and safe method of treating Epstein-Barr virus associated lymphomas; however, most lymphoma subtypes do not express EBV antigens. For these diseases, adoptive immunotherapy with genetically modified T cells expressing chimeric T cell receptors targeting lymphoma-associated antigens such as CD19 and CD20 appears to be a promising alternative. Recent innovations including enhanced co-stimulation, exogenous cytokine administration and use of memory T cells promise to overcome many of the limitations and pitfalls initially encountered with this approach.
化疗耐药性淋巴瘤可通过异基因造血细胞移植治愈,这表明这些肿瘤对T细胞介导的免疫反应敏感。然而,与移植相关的高发病率和死亡率限制了这种治疗方法。因此,人们努力开发基于T细胞的替代疗法,并且越来越多的证据表明,采用针对淋巴瘤相关抗原的T细胞进行过继性治疗可能是治疗这类疾病的一种安全有效的新方法。
目的/方法:我们综述了关于采用体外扩增的靶向病毒抗原的T细胞以及基因改造的自体T细胞进行过继性治疗作为淋巴瘤治疗策略的相关文献,目的是对这些方法进行概述。
结果/结论:爱泼斯坦-巴尔病毒特异性T细胞疗法是治疗爱泼斯坦-巴尔病毒相关淋巴瘤的一种有效且安全的方法;然而,大多数淋巴瘤亚型并不表达EBV抗原。对于这些疾病,采用表达靶向淋巴瘤相关抗原(如CD19和CD20)的嵌合T细胞受体的基因改造T细胞进行过继性免疫治疗似乎是一种有前景的替代方法。包括增强共刺激、给予外源性细胞因子以及使用记忆T细胞在内的最新创新有望克服最初在这种方法中遇到的许多限制和缺陷。