<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kadirkamanathan R</submitter><funding>RCUK | MRC | Medical Research Foundation</funding><funding>Medical Research Council</funding><funding>National Institute for Health Research (NIHR)</funding><funding>Wellcome Trust</funding><funding>Deutsche Krebshilfe (German Cancer Aid)</funding><pagination>2978-2987</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12634419</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>39(12)</volume><pubmed_abstract>Acute myeloid leukaemia (AML) is often aggressive and life-threatening with limited curative options. Immunotherapies including chimeric antigen receptor (CAR) T-cell approaches are under investigation, but high levels of disease heterogeneity remain a major hurdle to achieving durable responses. Targeting of multiple antigens may ensure complete immunological coverage of leukaemic blast populations, but such antigens are often also present on healthy haematopoietic populations. To address likely aplasia, strategies can be designed to bridge CAR T-cell therapies to allogeneic stem-cell transplantation (allo-SCT), as demonstrated in recent anti-CD7 CAR T-cell studies. Here we report that monotherapy using base edited "universal" donor CAR T cells against CD33, CLL-1, or CD7 delivered inhibi</pubmed_abstract><journal>Leukemia</journal><pubmed_title>Base edited "universal" donor CAR T-cell strategies for acute myeloid leukaemia.</pubmed_title><pmcid>PMC12634419</pmcid><funding_grant_id>MR/V03961X/1</funding_grant_id><funding_grant_id>RP-2014-05-007</funding_grant_id><funding_grant_id>70114706</funding_grant_id><funding_grant_id>MR/X004619/1</funding_grant_id><funding_grant_id>215619/Z/19/Z</funding_grant_id><funding_grant_id>MRF-045-0003-RG-GEOR-C0907</funding_grant_id><pubmed_authors>Heuser M</pubmed_authors><pubmed_authors>Etuk A</pubmed_authors><pubmed_authors>Georgiadis C</pubmed_authors><pubmed_authors>Kadirkamanathan R</pubmed_authors><pubmed_authors>Gough O</pubmed_authors><pubmed_authors>Schambach A</pubmed_authors><pubmed_authors>Sauer M</pubmed_authors><pubmed_authors>Qasim W</pubmed_authors><pubmed_authors>Kloos A</pubmed_authors><pubmed_authors>Joshi A</pubmed_authors><pubmed_authors>Preece R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Base edited "universal" donor CAR T-cell strategies for acute myeloid leukaemia.</name><description>Acute myeloid leukaemia (AML) is often aggressive and life-threatening with limited curative options. Immunotherapies including chimeric antigen receptor (CAR) T-cell approaches are under investigation, but high levels of disease heterogeneity remain a major hurdle to achieving durable responses. Targeting of multiple antigens may ensure complete immunological coverage of leukaemic blast populations, but such antigens are often also present on healthy haematopoietic populations. To address likely aplasia, strategies can be designed to bridge CAR T-cell therapies to allogeneic stem-cell transplantation (allo-SCT), as demonstrated in recent anti-CD7 CAR T-cell studies. Here we report that monotherapy using base edited "universal" donor CAR T cells against CD33, CLL-1, or CD7 delivered inhibi</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-06T06:39:26.517Z</modification><creation>2026-06-06T03:06:44.846Z</creation></dates><accession>S-EPMC12634419</accession><cross_references><pubmed>41034424</pubmed><doi>10.1038/s41375-025-02720-5</doi></cross_references></HashMap>