<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(9)</volume><submitter>Zhang C</submitter><pubmed_abstract>&lt;h4>Objectives&lt;/h4>Although adoptive cell therapy with T-cell receptor-engineered T cells (TCR-Ts) has mediated effective antitumor responses in several cancers, senescence of T cells could impair the therapeutic effect of TCR-Ts. Thus, it is essential to elucidate the characteristics of senescent TCR-Ts and how to subsequently improve their antitumor effect. Here, we focused on the influence of autophagy on TCR-Ts, since autophagy is tightly associated with the regulation of T-cell activation, proliferation and differentiation.&lt;h4>Methods&lt;/h4>We first evaluated autophagy level of senescent TCR-Ts, and then the senescent TCR-Ts were expanded &lt;i>in vitro&lt;/i> for 7 days with and without spermidine treatment, respectively. Furthermore, the proliferative potential, phenotypical characteristics</pubmed_abstract><journal>Clinical &amp; translational immunology</journal><pagination>e1419</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9512689</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Autophagic flux restoration of senescent T cells improves antitumor activity of TCR-engineered T cells.</pubmed_title><pmcid>PMC9512689</pmcid><pubmed_authors>Shen L</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Zhou P</pubmed_authors><pubmed_authors>Xiao Y</pubmed_authors><pubmed_authors>Lu Z</pubmed_authors><pubmed_authors>Teng X</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Autophagic flux restoration of senescent T cells improves antitumor activity of TCR-engineered T cells.</name><description>&lt;h4>Objectives&lt;/h4>Although adoptive cell therapy with T-cell receptor-engineered T cells (TCR-Ts) has mediated effective antitumor responses in several cancers, senescence of T cells could impair the therapeutic effect of TCR-Ts. Thus, it is essential to elucidate the characteristics of senescent TCR-Ts and how to subsequently improve their antitumor effect. Here, we focused on the influence of autophagy on TCR-Ts, since autophagy is tightly associated with the regulation of T-cell activation, proliferation and differentiation.&lt;h4>Methods&lt;/h4>We first evaluated autophagy level of senescent TCR-Ts, and then the senescent TCR-Ts were expanded &lt;i>in vitro&lt;/i> for 7 days with and without spermidine treatment, respectively. Furthermore, the proliferative potential, phenotypical characteristics</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-22T03:38:28.804Z</modification><creation>2025-04-05T20:46:31.698Z</creation></dates><accession>S-EPMC9512689</accession><cross_references><pubmed>36188121</pubmed><doi>10.1002/cti2.1419</doi></cross_references></HashMap>