<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>21(11)</volume><submitter>Ritchie DS</submitter><pubmed_abstract>In a phase I study of autologous chimeric antigen receptor (CAR) anti-LeY T-cell therapy of acute myeloid leukemia (AML), we examined the safety and postinfusion persistence of adoptively transferred T cells. Following fludarabine-containing preconditioning, four patients received up to 1.3 × 109 total T cells, of which 14-38% expressed the CAR. Grade 3 or 4 toxicity was not observed. One patient achieved a cytogenetic remission whereas another with active leukemia had a reduction in peripheral blood (PB) blasts and a third showed a protracted remission. Using an aliquot of In111-labeled CAR T cells, we demonstrated trafficking to the bone marrow (BM) in those patients with the greatest clinical benefit. Furthermore, in a patient with leukemia cutis, CAR T cells infiltrated proven sites of</pubmed_abstract><journal>Molecular therapy : the journal of the American Society of Gene Therapy</journal><pagination>2122-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3831035</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Persistence and efficacy of second generation CAR T cell against the LeY antigen in acute myeloid leukemia.</pubmed_title><pmcid>PMC3831035</pmcid><pubmed_authors>Peinert S</pubmed_authors><pubmed_authors>Scott AM</pubmed_authors><pubmed_authors>Honemann D</pubmed_authors><pubmed_authors>Chen K</pubmed_authors><pubmed_authors>Kravets L</pubmed_authors><pubmed_authors>Kershaw MH</pubmed_authors><pubmed_authors>Ritchie DS</pubmed_authors><pubmed_authors>Neeson PJ</pubmed_authors><pubmed_authors>Westwood JA</pubmed_authors><pubmed_authors>Khot A</pubmed_authors><pubmed_authors>Shin M</pubmed_authors><pubmed_authors>Trapani JA</pubmed_authors><pubmed_authors>Tainton K</pubmed_authors><pubmed_authors>Darcy PK</pubmed_authors><pubmed_authors>Prince HM</pubmed_authors><pubmed_authors>Dickinson M</pubmed_authors><pubmed_authors>Gambell P</pubmed_authors><pubmed_authors>Wall DM</pubmed_authors><pubmed_authors>Tai T</pubmed_authors><pubmed_authors>Westerman DA</pubmed_authors><pubmed_authors>Haurat J</pubmed_authors><pubmed_authors>Smyth MJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Persistence and efficacy of second generation CAR T cell against the LeY antigen in acute myeloid leukemia.</name><description>In a phase I study of autologous chimeric antigen receptor (CAR) anti-LeY T-cell therapy of acute myeloid leukemia (AML), we examined the safety and postinfusion persistence of adoptively transferred T cells. Following fludarabine-containing preconditioning, four patients received up to 1.3 × 109 total T cells, of which 14-38% expressed the CAR. Grade 3 or 4 toxicity was not observed. One patient achieved a cytogenetic remission whereas another with active leukemia had a reduction in peripheral blood (PB) blasts and a third showed a protracted remission. Using an aliquot of In111-labeled CAR T cells, we demonstrated trafficking to the bone marrow (BM) in those patients with the greatest clinical benefit. Furthermore, in a patient with leukemia cutis, CAR T cells infiltrated proven sites of</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Nov</publication><modification>2026-05-07T01:34:03.793Z</modification><creation>2026-04-07T22:27:53.393Z</creation></dates><accession>S-EPMC3831035</accession><cross_references><pubmed>23831595</pubmed><doi>10.1038/mt.2013.154</doi></cross_references></HashMap>