CAR-T: The Current and the Future

Kunal Mishra, Shun-Feng Zhou, Jiazhi Sun
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Abstract

Chimeric antigen receptors (CARs) are recombinant receptors that are expressed on autologous T-cells. CAR-T usage has grown in recent years as a way to combat hematological and solid tumors. The purpose of this review is to describe new studies on CAR-T treatment along with our lab’s ideas on potential uses and pitfalls that could be investigated. The usage of TREG and antiCLTA4 as means for regulating CAR-T will also be looked at along with OX40, CD137 and CD27 receptors as means for increasing the efficacy of the treatment overall. In addition the usage of iCasp9 as a ‘suicide switch’ for the CAR-T treatment and the potential for a 4th generation CAR will be touched upon. Then the review will lead into talks about how such a treatment could be of potential use in treating solid and hematological cancer.
CAR-T:现在和未来
嵌合抗原受体(CARs)是在自体t细胞上表达的重组受体。近年来,CAR-T作为一种对抗血液病和实体瘤的方法,其使用有所增长。这篇综述的目的是描述CAR-T治疗的新研究,以及我们实验室对潜在用途和可能研究的缺陷的想法。TREG和antiCLTA4作为调节CAR-T的手段也将与OX40、CD137和CD27受体一起被视为提高整体治疗效果的手段。此外,iCasp9作为CAR- t治疗的“自杀开关”的使用以及第四代CAR的潜力也将被提及。然后,该综述将引导讨论这种治疗方法如何在治疗实体癌和血液病方面具有潜在的用途。
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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