<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Krakow EF</submitter><funding>NCI NIH HHS</funding><pagination>1069-1082</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11406181</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>144(10)</volume><pubmed_abstract>&lt;h4>Abstract&lt;/h4>Relapse is the leading cause of death after allogeneic hematopoietic stem cell transplantation (HCT) for leukemia. T cells engineered by gene transfer to express T cell receptors (TCR; TCR-T) specific for hematopoietic-restricted minor histocompatibility (H) antigens may provide a potent selective antileukemic effect post-HCT. We conducted a phase 1 clinical trial using a novel TCR-T product targeting the minor H antigen, HA-1, to treat or consolidate treatment of persistent or recurrent leukemia and myeloid neoplasms. The primary objective was to evaluate the feasibility and safety of administration of HA-1 TCR-T after HCT. CD8+ and CD4+ T cells expressing the HA-1 TCR and a CD8 coreceptor were successfully manufactured from HA-1-disparate HCT donors. One or more infusion</pubmed_abstract><journal>Blood</journal><pubmed_title>HA-1-targeted T-cell receptor T-cell therapy for recurrent leukemia after hematopoietic stem cell transplantation.</pubmed_title><pmcid>PMC11406181</pmcid><funding_grant_id>P30 CA015704</funding_grant_id><funding_grant_id>K23 CA154532</funding_grant_id><pubmed_authors>Summers C</pubmed_authors><pubmed_authors>Kanaan SB</pubmed_authors><pubmed_authors>Black RG</pubmed_authors><pubmed_authors>Chapuis AG</pubmed_authors><pubmed_authors>Greenberg PD</pubmed_authors><pubmed_authors>Cunningham TM</pubmed_authors><pubmed_authors>Bleakley M</pubmed_authors><pubmed_authors>Denker AE</pubmed_authors><pubmed_authors>Biernacki MA</pubmed_authors><pubmed_authors>Gooley TA</pubmed_authors><pubmed_authors>Yeh AC</pubmed_authors><pubmed_authors>Vartanian N</pubmed_authors><pubmed_authors>Furlan SN</pubmed_authors><pubmed_authors>Yeung CCS</pubmed_authors><pubmed_authors>Brault M</pubmed_authors><pubmed_authors>Riddell SR</pubmed_authors><pubmed_authors>Till BG</pubmed_authors><pubmed_authors>Maloney DG</pubmed_authors><pubmed_authors>Bar M</pubmed_authors><pubmed_authors>Krakow EF</pubmed_authors><pubmed_authors>Dahlberg A</pubmed_authors><pubmed_authors>Cassaday RD</pubmed_authors><pubmed_authors>Woodward KB</pubmed_authors><pubmed_authors>Dossa RG</pubmed_authors><pubmed_authors>Newell EW</pubmed_authors></additional><is_claimable>false</is_claimable><name>HA-1-targeted T-cell receptor T-cell therapy for recurrent leukemia after hematopoietic stem cell transplantation.</name><description>&lt;h4>Abstract&lt;/h4>Relapse is the leading cause of death after allogeneic hematopoietic stem cell transplantation (HCT) for leukemia. T cells engineered by gene transfer to express T cell receptors (TCR; TCR-T) specific for hematopoietic-restricted minor histocompatibility (H) antigens may provide a potent selective antileukemic effect post-HCT. We conducted a phase 1 clinical trial using a novel TCR-T product targeting the minor H antigen, HA-1, to treat or consolidate treatment of persistent or recurrent leukemia and myeloid neoplasms. The primary objective was to evaluate the feasibility and safety of administration of HA-1 TCR-T after HCT. CD8+ and CD4+ T cells expressing the HA-1 TCR and a CD8 coreceptor were successfully manufactured from HA-1-disparate HCT donors. One or more infusion</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Sep</publication><modification>2026-05-29T19:46:38.973Z</modification><creation>2026-04-08T05:51:04.252Z</creation></dates><accession>S-EPMC11406181</accession><cross_references><pubmed>38683966</pubmed><doi>10.1182/blood.2024024105</doi></cross_references></HashMap>