Harnessing Chimeric Antigen Receptor-engineered Invariant Natural Killer T Cells: Therapeutic Strategies for Cancer and the Tumor Microenvironment

被引:1
作者
Wang, Yiqing [1 ]
Li, Yan-Ruide [2 ]
机构
[1] Univ Washington, Dept Chem, Biochem, Seattle, WA 98105 USA
[2] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
关键词
Invariant natural killer T cell; chimeric antigen receptor; cancer immunotherapy; tumor microenvironment; genetic engineering; autologous therapy; allogeneic therapy; graft-versus-host disease; off-the-shelf cancer therapy; V-ALPHA-24-INVARIANT NKT CELLS; ANTITUMOR-ACTIVITY; SUPPRESSOR-CELLS; DISTINCT SUBSETS; CAR THERAPY; INKT CELLS; CD19; IMMUNITY; IMMUNOTHERAPY; CYTOTOXICITY;
D O I
10.2174/0113892010265228231116073012
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
Chimeric antigen receptor (CAR)-engineered T (CAR-T) cell therapy has emerged as a revolutionary approach for cancer treatment, especially for hematologic cancers. However, CAR-T therapy has some limitations, including cytokine release syndrome (CRS), immune cell-associated neurologic syndrome (ICANS), and difficulty in targeting solid tumors and delivering allogeneic cell therapy due to graft-versus-host disease (GvHD). Therefore, it is important to explore other cell sources for CAR engineering. Invariant natural killer T (iNKT) cells are a potential target, as they possess powerful antitumor ability and do not recognize mismatched major histocompatibility complexes (MHCs) and protein antigens, thus avoiding the risk of GvHD. CAR-engineered iNKT (CAR-iNKT) cell therapy offers a promising new approach to cancer immunotherapy by overcoming the drawbacks of CAR-T cell therapy while retaining potent antitumor capabilities. This review summarizes the current CAR-iNKT cell products, their functions and phenotypes, and their potential for off-the-shelf cancer immunotherapy.
引用
收藏
页码:2001 / 2011
页数:11
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