<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/GSE328nnn/GSE328705/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</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=GSE328705</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Divergent Cytotoxic and Inflammatory Functions of Intratumoral Vd2+ gdT Cells in Renal Cell Carcinoma</name><description>We characterized Vd2+ gdT cell subsets in paired peripheral blood and tumor samples from three treatment-naive clear cell renal cell carcinoma (ccRCC) patients using flow cytometry and single-cell RNA sequencing. Two major subsets distinguished by CD16 expression exhibited divergent cytotoxic and inflammatory effector programs within the tumor microenvironment. Single-cell RNA sequencing identified four transcriptional clusters with a TOX+ progenitor-like cluster giving rise to divergent effector states.</description><dates><publication>2026/08/06</publication></dates><accession>GSE328705</accession><cross_references><GSM>GSM9687954</GSM><GSM>GSM9687955</GSM><GSM>GSM9687956</GSM><GPL>24676</GPL><GSE>328705</GSE><taxon>Homo sapiens</taxon><PMID>[42539629]</PMID></cross_references></HashMap>