ErbB-targeted CAR T-cell immunotherapy of cancer

被引:10
作者
Whilding, Lynsey M. [1 ]
Maher, John [1 ]
机构
[1] Kings Coll London, Kings Hlth Partners Integrated Canc Ctr, Dept Res Oncol, London SE1 9RT, England
基金
英国惠康基金;
关键词
cancer; chimeric antigen receptor; ErbB receptors; HER2; immunotherapy; T cells; CHIMERIC ANTIGEN RECEPTOR; GROWTH-FACTOR RECEPTOR; CYTOKINE RELEASE; GENETIC-MODIFICATION; ANTITUMOR-ACTIVITY; ENHANCED SURVIVAL; BREAST-CANCER; STEM-CELLS; EGFRVIII; GLIOMA;
D O I
10.2217/IMT.14.120
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chimeric antigen receptor (CAR) based immunotherapy has been under development for the last 25 years and is now a promising new treatment modality in the field of cancer immunotherapy. The approach involves genetically engineering T cells to target malignant cells through expression of a bespoke fusion receptor that couples an HLA-independent antigen recognition domain to one or more intracellular T-cell activating modules. Multiple clinical trials are now underway in several centers to investigate CAR T-cell immunotherapy of diverse hematologic and solid tumor types. The most successful results have been achieved in the treatment of patients with B-cell malignancies, in whom several complete and durable responses have been achieved. This review focuses on the preclinical and clinical development of CAR T-cell immunotherapy of solid cancers, targeted against members of the ErbB family.
引用
收藏
页码:229 / 241
页数:13
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