[Cell therapy's poster child: Chimeric antigen receptor T cell therapy]

Sheng Wu Gong Cheng Xue Bao. 2019 Dec 25;35(12):2339-2349. doi: 10.13345/j.cjb.190291.
[Article in Chinese]

Abstract

Chimeric antigen receptor T (CAR-T) cell therapy, which adoptively transfers engineered T cells expressing synthetic receptors to target specific antigens, has achieved great clinical success in treating hematological malignancies. Though FDA has approved two CAR-T products, CAR-T therapy can cause some side effects, such as cytokine release syndrome (CRS), neurotoxicity and B cell aplasia. Meanwhile, lacking tumor specific antigen and the suppressive tumor environment limit the efficacy of CAR-T therapy in solid tumor. This review focuses on the structural components, clinical applications and synthetic biology approaches on CAR-T cell design, and summarizes the challenges and perspectives of CAR-T therapy as a revolutionary cancer immunotherapy.

嵌合抗原受体T (CAR-T) 细胞疗法是一种利用合成受体特异性靶向抗原的过继性细胞疗法(ACT),目前在血液肿瘤的治疗中有极大的临床应用价值。虽然美国食品药品监督管理局 (FDA) 已经批准两款CAR-T 药物上市,但CAR-T 疗法在治疗过程中仍然存在一些副作用,如细胞因子释放综合征 (CRS)、神经毒性、B 细胞功能缺失等。同时,CAR-T 疗法在实体瘤治疗中的效果甚微,主要原因是缺乏特异性靶点以及肿瘤微环境对CAR-T 细胞功能的抑制等。文中将从CAR 的结构设计、临床应用、合成生物学对新型CAR 的优化来阐述应用CAR-T 细胞疗法治疗肿瘤所面临的挑战及广阔前景。.

Keywords: cell therapy; chimeric antigen receptor T cell; immunotherapy; synthetic biology.

Publication types

  • Review

MeSH terms

  • Cell- and Tissue-Based Therapy*
  • Child
  • Humans
  • Immunotherapy
  • Immunotherapy, Adoptive*
  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen
  • T-Lymphocytes

Substances

  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen