<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhao Q</submitter><funding>Ministry of Science and Technology of the People's Republic of China (MOST)</funding><funding>Guangdong Provincial Key Laboratory of Construction Foundation ()</funding><funding>Guangzhou Municipal Science and Technology Bureau (GZST)</funding><funding>Guangdong Special Support Plan ()</funding><funding>Sun Yat-sen University (SYSU)</funding><pagination>3886-3896</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12434392</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>31(18)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>This study aimed to preliminarily evaluate the safety, tolerability, and antitumor efficacy of hepatitis B virus (HBV)-specific T-cell receptor (TCR)-T cell therapy combining mRNA electroporation and lentiviral transduction in patients with recurrent HBV-hepatocellular carcinoma after liver transplantation.&lt;h4>Patients and methods&lt;/h4>In this pilot study (NCT04677088), two types of autologous HBV-specific TCR-redirected T cells were assessed without prior lymphodepletion: (i) multiple infusions of mRNA-electroporated HBV-TCR-T cells (mRNA-HBV-TCR-T cells) and (ii) one to three infusions of lentiviral-transduced HBV-TCR-T cells (lenti-HBV-TCR-T cells). Treatment-related adverse events were assessed using the Common Terminology Criteria for Adverse Events, and antitumor effic</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>HBV-Specific TCR-T Cell Therapy Combining mRNA Electroporation and Lentiviral Transduction: Treatment Regimen for Recurrent HBV-Related HCC after Liver Transplantation.</pubmed_title><pmcid>PMC12434392</pmcid><funding_grant_id>R07015</funding_grant_id><funding_grant_id>2023YFF1501200</funding_grant_id><funding_grant_id>2020B1212060026</funding_grant_id><funding_grant_id>2024A04J6388</funding_grant_id><funding_grant_id>82470687</funding_grant_id><funding_grant_id>82404650</funding_grant_id><funding_grant_id>R70004</funding_grant_id><funding_grant_id>2024B03J1235</funding_grant_id><funding_grant_id>Y-2023-756</funding_grant_id><funding_grant_id>2023YFF1501202</funding_grant_id><funding_grant_id>82270686</funding_grant_id><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Koh S</pubmed_authors><pubmed_authors>Tan H</pubmed_authors><pubmed_authors>Guo Z</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Qin M</pubmed_authors><pubmed_authors>Wai LE</pubmed_authors><pubmed_authors>Dan J</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Zhao Q</pubmed_authors><pubmed_authors>Wang T</pubmed_authors><pubmed_authors>He X</pubmed_authors><pubmed_authors>Luo W</pubmed_authors><pubmed_authors>Wong RWJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>HBV-Specific TCR-T Cell Therapy Combining mRNA Electroporation and Lentiviral Transduction: Treatment Regimen for Recurrent HBV-Related HCC after Liver Transplantation.</name><description>&lt;h4>Purpose&lt;/h4>This study aimed to preliminarily evaluate the safety, tolerability, and antitumor efficacy of hepatitis B virus (HBV)-specific T-cell receptor (TCR)-T cell therapy combining mRNA electroporation and lentiviral transduction in patients with recurrent HBV-hepatocellular carcinoma after liver transplantation.&lt;h4>Patients and methods&lt;/h4>In this pilot study (NCT04677088), two types of autologous HBV-specific TCR-redirected T cells were assessed without prior lymphodepletion: (i) multiple infusions of mRNA-electroporated HBV-TCR-T cells (mRNA-HBV-TCR-T cells) and (ii) one to three infusions of lentiviral-transduced HBV-TCR-T cells (lenti-HBV-TCR-T cells). Treatment-related adverse events were assessed using the Common Terminology Criteria for Adverse Events, and antitumor effic</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-02T05:27:32.858Z</modification><creation>2026-04-14T03:14:17.377Z</creation></dates><accession>S-EPMC12434392</accession><cross_references><pubmed>40705079</pubmed><doi>10.1158/1078-0432.CCR-25-1245</doi></cross_references></HashMap>