<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE312nnn/GSE312099/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE312099</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Immune cell sequencing after allogeneic hematopoietic cell transplantation [snATAC-seq]</name><description>Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a curative therapy for hematologic malignancies. The primary non-relapse complication after allo-HSCT is graft-versus-host disease (GVHD). The use of T regulatory (Treg) cells to prevent GVHD has emerged as a promising allogeneic T cell immunotherapy in the form of Orca-T. However, the precise differences in immune states which may influence clinical outcomes after Orca-T compared with unmanipulated peripheral blood stem cell (PBSC) grafts remain unexplored. Using peripheral blood specimens longitudinally collected between 3 weeks and one year after leukemia treatment, we examined single-nucleus ATAC-seq and whole transcriptome sequencing (scRNA-seq) analysis of PBMC from 4 patients receiving either Orca-T or unmanipulated PBSC grafts and 2 mobilized donors.</description><dates><publication>2026/05/27</publication></dates><accession>GSE312099</accession><cross_references><GSM>GSM9337724</GSM><GSM>GSM9337723</GSM><GPL>24676</GPL><GSE>312099</GSE><taxon>Homo sapiens</taxon><PMID>[41758930]</PMID></cross_references></HashMap>