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Driving better and safer HER2-specific CARs for cancer therapy

期刊

ONCOTARGET
卷 8, 期 37, 页码 62730-62741

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.17528

关键词

chimeric antigen receptor; HER2; cancer; immunotherapy; toxicity

资金

  1. National Science Foundation for Young Scientists of China [81602709, 81502525]
  2. Natural Science Foundation of Shandong Province [ZR2015YL031, ZR2015PH012]

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Given the clinical efficacy of chimeric antigen receptor (CAR)-based therapy in hematological malignancies, CAR T-cell therapy for a number of solid tumors has been actively investigated. Human epidermal growth factor receptor 2 (HER2) is a well-established therapeutic target in breast, as well as other types of cancer. However, HER2 CAR T cells pose a risk of lethal toxicity including cytokine release syndrome from on-target, off-tumor recognition of HER2. In this review, we summarize the development of conventional HER2 CAR technology, the alternative selection of CAR hosts, the novel HER2 CAR designs, clinical studies and toxicity. Furthermore, we also discuss the main strategies for improving the safety of HER2 CAR-based cancer therapies.

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