<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ecsedi M</submitter><funding>Fred Hutchinson Cancer Research Center</funding><funding>MPN Research Foundation</funding><funding>NCI NIH HHS</funding><funding>NIH</funding><funding>Damon Runyon Cancer Research Foundation</funding><pagination>48-56</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7770096</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(1)</volume><pubmed_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.</pubmed_abstract><journal>Trends in cancer</journal><pubmed_title>The Anticancer Potential of T Cell Receptor-Engineered T Cells.</pubmed_title><pmcid>PMC7770096</pmcid><funding_grant_id>CA18029-39</funding_grant_id><funding_grant_id>P01 CA225517</funding_grant_id><funding_grant_id>P01 CA018029</funding_grant_id><funding_grant_id>CA225517-01</funding_grant_id><pubmed_authors>McAfee MS</pubmed_authors><pubmed_authors>Ecsedi M</pubmed_authors><pubmed_authors>Chapuis AG</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Anticancer Potential of T Cell Receptor-Engineered T Cells.</name><description>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.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jan</publication><modification>2025-04-04T13:12:18.154Z</modification><creation>2022-02-11T14:02:12.52Z</creation></dates><accession>S-EPMC7770096</accession><cross_references><pubmed>32988787</pubmed><doi>10.1016/j.trecan.2020.09.002</doi></cross_references></HashMap>