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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.
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页码:229 / 241
页数:13
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