Future perspectives on engineered T cells for cancer

被引:0
|
作者
Posey Jr, Avery D. [1 ,2 ,3 ,5 ]
Young, Regina M. [1 ,3 ,4 ]
June, Carl H. [1 ,3 ,4 ]
机构
[1] Univ Penn, Ctr Cellular Immunotherapies, Perelman Sch Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Dept Syst Pharmacol & Translat Therapeut, Philadelphia, PA 19103 USA
[3] Univ Penn, Parker Inst Canc Immunotherapy, Philadelphia, PA 19104 USA
[4] Univ Penn, Perelman Sch Med, Dept Pathol & Lab Med, Philadelphia 19104, PA USA
[5] Corporal Michael J Crescenz VA Med Ctr, Philadelphia, PA USA
关键词
INTERLEUKIN-12; IMMUNOTHERAPY; NEUROTOXICITY; METABOLISM; ACTIVATION; EFFICACY; THERAPY; TUMORS; CD19;
D O I
10.1016/j.trecan.2024.05.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chimeric antigen receptor (CAR) T cell therapy has emerged as a revolutionary treatment for hematological malignancies, but its adaptation to solid tumors is impeded by multiple challenges, particularly T cell dysfunction and exhaustion. The heterogeneity and inhospitableness of the solid tumor microenvironment (TME) contribute to diminished CAR T cell efficacy exhibited by reduced cytotoxicity, proliferation, cytokine secretion, and the upregulation of inhibitory receptors, similar to the phenotype of tumor-infiltrating lymphocytes (TILs). In this review, we highlight recent advances in T cell therapy for solid tumors, particularly brain cancer. Innovative strategies, including locoregional delivery and 'armoring' CAR T cells with cytokines such as interleukin (IL)-18, are under investigation to improve efficacy and safety. We also highlight emerging issues with toxicity management of CAR T cell adverse events. This review discusses the obstacles associated with CAR T cell therapy in the context of solid tumors and outlines current and future strategies to overcome these challenges.
引用
收藏
页码:687 / 695
页数:9
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