| Literature DB >> 25804476 |
Lynsey M Whilding1, John Maher.
Abstract
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.Entities:
Keywords: ErbB receptors; HER2; T cells; cancer; chimeric antigen receptor; immunotherapy
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Year: 2015 PMID: 25804476 DOI: 10.2217/imt.14.120
Source DB: PubMed Journal: Immunotherapy ISSN: 1750-743X Impact factor: 4.196