Alternative CAR Therapies: Recent Approaches in Engineering Chimeric Antigen Receptor Immune Cells to Combat Cancer

被引:21
作者
Moreno, Carlos [1 ]
Haynie, Christopher [1 ]
Cheever, Abigail [1 ]
Weber, K. Scott [1 ]
机构
[1] Brigham Young Univ, Dept Microbiol & Mol Biol, Provo, UT 84602 USA
关键词
T cell; chimeric antigen receptor; CAR; NK cell; macrophage; autoimmune; cancer; immunotherapy; autoreactive B cell; cytotoxicity; NATURAL-KILLER-CELLS; REGULATORY T-CELLS; TUMOR-ASSOCIATED MACROPHAGES; ADOPTIVE TRANSFER; IN-VITRO; VIVO EXPANSION; NK-92; CELLS; NK CELLS; B-CELLS; EXPRESSION;
D O I
10.3390/biomedicines10071493
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
For nearly three decades, chimeric antigen receptors (CARs) have captivated the interest of researchers seeking to find novel immunotherapies to treat cancer. CARs were first designed to work with T cells, and the first CAR T cell therapy was approved to treat B cell lymphoma in 2017. Recent advancements in CAR technology have led to the development of modified CARs, including multi-specific CARs and logic gated CARs. Other immune cell types, including natural killer (NK) cells and macrophages, have also been engineered to express CARs to treat cancer. Additionally, CAR technology has been adapted in novel approaches to treating autoimmune disease and other conditions and diseases. In this article, we review these recent advancements in alternative CAR therapies and design, as well as their mechanisms of action, challenges in application, and potential future directions.
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页数:31
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