<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Guo H</submitter><funding>National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>1172-1185</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8093297</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(5)</volume><pubmed_abstract>Haploidentical stem cell transplantation (haplo-SCT) achieves superior or at least comparable clinical outcomes to HLA-matched sibling donor transplantation (MSDT) in treating hematological malignancies. To define the underlying regulatory dynamics, we analyzed time courses of leukemia burden and immune abundance of haplo-SCT or MSDT from multiple dimension. First, we employed two nonirradiated leukemia mouse models which carried human AML-ETO or MLL-AF9 fusion gene to establish haplo-identical and major histocompatibility (MHC)-matched transplantation models and investigated the immune cell dynamic response during leukemia development in vivo. We found that haplo-matching the MHCs of leukemia cells with recipient mouse T cells prolonged leukemic mice survival and reduced leukemia burden. </pubmed_abstract><journal>Cellular &amp; molecular immunology</journal><pubmed_title>Dynamic immune profiling identifies the stronger graft-versus-leukemia (GVL) effects with haploidentical allografts compared to HLA-matched stem cell transplantation.</pubmed_title><pmcid>PMC8093297</pmcid><funding_grant_id>81621001</funding_grant_id><pubmed_authors>Chang YJ</pubmed_authors><pubmed_authors>Wang FR</pubmed_authors><pubmed_authors>Sun YQ</pubmed_authors><pubmed_authors>Xu LP</pubmed_authors><pubmed_authors>Chen H</pubmed_authors><pubmed_authors>Wang M</pubmed_authors><pubmed_authors>Zhang XH</pubmed_authors><pubmed_authors>Tang FF</pubmed_authors><pubmed_authors>Huang XJ</pubmed_authors><pubmed_authors>Hong Y</pubmed_authors><pubmed_authors>Guo H</pubmed_authors><pubmed_authors>Wei-Han</pubmed_authors><pubmed_authors>Yan CH</pubmed_authors><pubmed_authors>Chen YH</pubmed_authors><pubmed_authors>Mo XD</pubmed_authors><pubmed_authors>Liu KY</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dynamic immune profiling identifies the stronger graft-versus-leukemia (GVL) effects with haploidentical allografts compared to HLA-matched stem cell transplantation.</name><description>Haploidentical stem cell transplantation (haplo-SCT) achieves superior or at least comparable clinical outcomes to HLA-matched sibling donor transplantation (MSDT) in treating hematological malignancies. To define the underlying regulatory dynamics, we analyzed time courses of leukemia burden and immune abundance of haplo-SCT or MSDT from multiple dimension. First, we employed two nonirradiated leukemia mouse models which carried human AML-ETO or MLL-AF9 fusion gene to establish haplo-identical and major histocompatibility (MHC)-matched transplantation models and investigated the immune cell dynamic response during leukemia development in vivo. We found that haplo-matching the MHCs of leukemia cells with recipient mouse T cells prolonged leukemic mice survival and reduced leukemia burden. </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 May</publication><modification>2025-04-04T10:15:49.855Z</modification><creation>2025-04-04T10:15:49.855Z</creation></dates><accession>S-EPMC8093297</accession><cross_references><pubmed>33408344</pubmed><doi>10.1038/s41423-020-00597-1</doi></cross_references></HashMap>