| Literature DB >> 28613086 |
Benjamin Demoulin1, W James Cook2, Joana Murad3, David J Graber2, Marie-Louise Sentman2, Caroline Lonez1, David E Gilham1, Charles L Sentman2, Sophie Agaugue1.
Abstract
Chimeric antigen receptors (CARs) are genetically engineered proteins that combine an extracellular antigen-specific recognition domain with one or several intracellular T-cell signaling domains. When expressed in T cells, these CARs specifically trigger T-cell activation upon antigen recognition. While the clinical proof of principle of CAR T-cell therapy has been established in hematological cancers, CAR T cells are only at the early stages of being explored to tackle solid cancers. This special report discusses the concept of exploiting natural killer cell receptors as an approach that could broaden the specificity of CAR T cells and potentially enhance the efficacy of this therapy against solid tumors. New data demonstrating feasibility of this approach in humans and supporting the ongoing clinical trial are also presented.Entities:
Keywords: CAR-T; CM-CS1; NKG2D; NKR-2; adoptive cell therapy; chimeric antigen receptor; clinical trial; immunotherapy; pancreatic cancer
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Year: 2017 PMID: 28613086 DOI: 10.2217/fon-2017-0102
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404