Exploring the mechanisms of CD19 CAR T-cell failure and salvage strategies in B-cell lymphoma

Fan Yang, Rui Liu, K. Hu
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Abstract

Chimeric antigen receptor (CAR) T-cell therapy has emerged as a potential treatment for patients with B-cell lymphoma in whom standard therapy has failed. The U.S. Food and Drug Administration (FDA) has approved anti-CD19 CAR T-cell products for B-cell lymphoma. However, growing experience has shown that treatment has limitations, such as relapses due to tumour mutations or CD19 antigen loss, unexpanded CAR T-cells, and/or poor persistence of CAR T-cells. Understanding the limitations of CAR T-cell therapy is essential to achieve the full potential of this therapeutic strategy. In this review, we analyse factors potentially affecting the efficacy of CAR T-cell therapy, explore the mechanisms of resistance to CD19 CAR T-cell therapy in B-cell lymphoma, and summarise potential strategies to overcome treatment barriers.
探讨b细胞淋巴瘤中CD19 CAR - t细胞衰竭的机制和挽救策略
嵌合抗原受体(CAR) t细胞疗法已成为标准治疗失败的b细胞淋巴瘤患者的潜在治疗方法。美国食品和药物管理局(FDA)已批准抗cd19 CAR - t细胞产品治疗b细胞淋巴瘤。然而,越来越多的经验表明,治疗有局限性,如由于肿瘤突变或CD19抗原丢失、CAR - t细胞未扩增和/或CAR - t细胞持久性差而复发。了解CAR - t细胞疗法的局限性对于充分发挥这种治疗策略的潜力至关重要。在这篇综述中,我们分析了可能影响CAR - t细胞治疗疗效的因素,探讨了b细胞淋巴瘤对CD19 CAR - t细胞治疗的耐药机制,并总结了克服治疗障碍的潜在策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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