CAR‐T‐cell products in solid tumors: Progress, challenges, and strategies

Author:

Qian Kewen12,Li Guangyao23,Zhang Shuyi23,Fu Wenyan4,Li Tian23,Zhao Jian5,Lei Changhai23,Wang Yuqing6,Hu Shi12ORCID

Affiliation:

1. Department of Biomedical Engineering College of Basic Medical Sciences Naval Medical University Shanghai China

2. Team NMU‐China of the International Genetically Engineered Machine (iGEM) Competition Department of Biophysics Naval Medical University Shanghai China

3. Department of Biophysics College of Basic Medical Sciences Naval Medical University Shanghai China

4. Department of Assisted Reproduction Shanghai Ninth People's Hospital Shanghai Jiao Tong University School of Medicine Shanghai China

5. KOCHKOR Biotech, Inc. Shanghai China

6. Department of Medicine and Biosystemic Science Faculty of Medical Sciences Kyushu University Fukuoka Japan

Abstract

AbstractT cells engineered to express chimeric antigen receptors (CARs) with specificity toward tumor cells have led to promising outcomes in patients with hematological malignancies. Nevertheless, the application of CAR‐T cell therapy in solid tumors encounters several obstacles. These include tumor heterogeneity and immune escape, T cell exhaustion and restricted infiltration into the tumors that affect the therapeutic efficacy of CAR‐T cells, as well as “on‐target, off‐tumor” toxicities that can lead to severe and even fatal adverse events. In recent years, clinical trials and new approaches of CAR‐T cell therapy for solid tumors have made certain progress. Here, we update the outcomes of related clinical trials and summarize engineered strategies aiming to improve the efficacy and therapeutic safety of CAR‐T cells based on experimental and clinical studies.

Publisher

Wiley

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