<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/GSE330nnn/GSE330958/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE330958</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Leveraging TNFR2 for antitumour immunity: Treg depletion and myeloid reprogramming versus T cell costimulation</name><description>We conducted single-cell RNA sequencing using the 10x Genomics Chromium Next-GEM Flex protocol to investigate the mechanism of action of two TNFR2-targeting antibodies—one ligand-blocking and the other agonistic. Our goal was to assess their anti-cancer potential in comparison to established immune checkpoint inhibitors, anti-PD1 and anti-CTLA4. These studies provide new insights and role of TNFR2 as a therapeutic target in cancer.</description><dates><publication>2026/07/09</publication></dates><accession>GSE330958</accession><cross_references><GSM>GSM9736509</GSM><GSM>GSM9736507</GSM><GSM>GSM9736508</GSM><GSM>GSM9736516</GSM><GSM>GSM9736517</GSM><GSM>GSM9736514</GSM><GSM>GSM9736515</GSM><GSM>GSM9736512</GSM><GSM>GSM9736513</GSM><GSM>GSM9736510</GSM><GSM>GSM9736511</GSM><GPL>24247</GPL><GSE>330958</GSE><taxon>Mus musculus</taxon><PMID>[42466984]</PMID></cross_references></HashMap>