| Literature DB >> 32988787 |
Matyas Ecsedi1, Megan S McAfee1, Aude G Chapuis2.
Abstract
Adoptively transferred T cell receptor (TCR)-transgenic T cells (TCR-T cells) are not restricted by cell surface expression of their targets and are therefore poised to become a main pillar of cellular cancer immunotherapies. Addressing clinical and laboratory data, we discuss emerging features for the efficient deployment of novel TCR-T therapies, such as selection of ideal TCRs targeting validated epitopes with well-characterized cancer cell expression and processing, enhancing TCR-T effector function, trafficking, expansion, persistence, and memory formation by strategic selection of substrate cells, and gene-engineering with synthetic co-stimulatory circuits. Overall, a better understanding of the relevant mechanisms of action and resistance will help prioritize the vast array of potential TCR-T optimizations for future clinical products.Entities:
Keywords: TCR-T; cancer immunotherapy; engineered T cells
Mesh:
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Year: 2020 PMID: 32988787 PMCID: PMC7770096 DOI: 10.1016/j.trecan.2020.09.002
Source DB: PubMed Journal: Trends Cancer ISSN: 2405-8025