Chimeric-Antigen-Receptor (CAR) T Cells and the Factors Influencing their Therapeutic Efficacy.

Victoria G Kravets, Yi Zhang, Hongxing Sun
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Abstract

Immunotherapeutic treatments for malignant cancers have revolutionized the medical and scientific fields. Lymphocytes engineered to display chimeric antigen receptor (CAR) molecules contribute to the exciting advancements that have stemmed from a greater understanding of cell structure and function, biological interactions, and the unique tumor microenvironment. CAR T cells circumvent the unique immune evasion capability of tumors by acting in a major histocompatibility complex (MHC) independent manner. Various factors contribute to the efficacy of CAR therapy, including CAR structure, gene transfer strategies, in vitro culture system, target selection, and preconditioning regimens. While recent clinical trials have shown promising success, cytotoxicity and other various challenges need to be addressed before CAR therapy can reach its full clinical potency. This review will discuss factors associated with CAR therapeutic success and the difficulties that continue to be a focus of research around the world.

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嵌合抗原受体(CAR) T细胞及其疗效影响因素。
恶性癌症的免疫治疗已经彻底改变了医学和科学领域。淋巴细胞工程显示嵌合抗原受体(CAR)分子有助于令人兴奋的进步,这源于对细胞结构和功能,生物相互作用和独特肿瘤微环境的更深入了解。CAR - T细胞通过独立于主要组织相容性复合体(MHC)的方式规避肿瘤独特的免疫逃避能力。影响CAR治疗效果的因素有很多,包括CAR结构、基因转移策略、体外培养系统、靶点选择和预处理方案。虽然最近的临床试验显示出有希望的成功,但在CAR治疗达到其全部临床效力之前,需要解决细胞毒性和其他各种挑战。这篇综述将讨论与CAR治疗成功相关的因素以及仍然是世界范围内研究的焦点的困难。
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