Emory Vaccine Center, Department of Microbiology & Immunology, Emory University School of Medicine, 1510 Clifton Road, Room G211, Atlanta, GA 30322, USA.
Immunotherapy. 2013 Sep;5(9):975-87. doi: 10.2217/imt.13.91.
During chronic infections and cancer, T cells progressively lose function and become exhausted. However, effective T-cell responses are necessary to ultimately control viral infections and tumors. Hence, strategies that either restore endogenous immune responses or provide functional T cells by adoptive immunotherapy need to be explored. CD8 T cells play a prominent role in viral infections, as well as cancer, but CD4 T cells are necessary to support CD8 T-cell function. In addition, CD4 T cells exert direct effector functions, induce optimal B-cell responses and orchestrate innate immunity. Therefore, we propose that adoptive transfer strategies should exploit CD4 T cells alone or in combination with CD8 T cells, for the treatment of chronic infections and cancer. Furthermore, since adoptively transferred cells are subject to exhaustion, combining adoptive transfer therapy with immunotherapies that inhibit T-cell exhaustion should maximize the longevity and success rate of responses.
在慢性感染和癌症中,T 细胞逐渐失去功能并衰竭。然而,有效的 T 细胞反应对于最终控制病毒感染和肿瘤是必要的。因此,需要探索恢复内源性免疫反应或通过过继免疫疗法提供功能性 T 细胞的策略。CD8 T 细胞在病毒感染以及癌症中发挥重要作用,但 CD4 T 细胞对于支持 CD8 T 细胞功能是必需的。此外,CD4 T 细胞发挥直接效应功能,诱导最佳的 B 细胞反应,并协调先天免疫。因此,我们提出,过继转移策略应单独或联合使用 CD8 T 细胞来治疗慢性感染和癌症。此外,由于过继转移细胞会衰竭,因此将过继转移治疗与抑制 T 细胞衰竭的免疫疗法相结合,应能最大限度地延长反应的持久性和成功率。