Asokan Sahana, Cullin Nyssa, Stein-Thoeringer Christoph K, Elinav Eran
Division of Microbiome and Cancer, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany.
Faculty of Biosciences, Heidelberg University, 69120 Heidelberg, Germany.
Cancers (Basel). 2023 Jan 28;15(3):794. doi: 10.3390/cancers15030794.
Chimeric antigen receptor (CAR) - T cell cancer therapy has yielded promising results in treating hematologic malignancies in clinical studies, and a growing number of CAR-T regimens are approved for clinical usage. While the therapy is considered of great potential in expanding the cancer immunotherapy arsenal, more than half of patients receiving CAR-T infusions do not respond, while others develop significant adverse effects, collectively indicating a need for optimization of CAR-T treatment to the individual. The microbiota is increasingly suggested as a major modulator of immunotherapy responsiveness. Studying causal microbiota roles possibly contributing to CAR-T therapy efficacy, adverse effects reduction, and prediction of patient responsiveness constitutes an exciting area of active research. Herein, we discuss the latest developments implicating human microbiota involvement in CAR-T therapy, while highlighting challenges and promises in harnessing the microbiota as a predictor and modifier of CAR-T treatment towards optimized efficacy and minimization of treatment-related adverse effects.
嵌合抗原受体(CAR)-T细胞癌症疗法在临床研究中治疗血液系统恶性肿瘤已取得了令人鼓舞的成果,并且越来越多的CAR-T治疗方案已获批用于临床。虽然该疗法在扩充癌症免疫治疗武器库方面被认为具有巨大潜力,但超过一半接受CAR-T输注的患者没有反应,而其他患者则出现了严重的不良反应,这共同表明需要针对个体优化CAR-T治疗。越来越多的研究表明,微生物群是免疫治疗反应性的主要调节因子。研究微生物群在CAR-T治疗疗效、减少不良反应以及预测患者反应性方面可能发挥的因果作用,构成了一个令人兴奋的活跃研究领域。在此,我们讨论了涉及人类微生物群参与CAR-T治疗的最新进展,同时强调了利用微生物群作为CAR-T治疗的预测指标和调节因子以实现最佳疗效并将治疗相关不良反应降至最低所面临的挑战和前景。