<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/GSE347nnn/GSE347031/</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=GSE347031</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Therapeutic HPV16 E7 Vaccination with CD137 Agonism Induces Tumour Regression and Durable Immunity in Mice</name><description>Therapeutic HPV16 E7 vaccination was evaluated in the syngeneic TC-1 tumour model in female C57BL/6 mice. Bulk RNA sequencing was performed on pooled, non-adherent mononuclear cell-enriched fractions prepared from subcutaneous tumour samples. The dataset compares PBS or vehicle controls, MPLA-adjuvanted wild-type E7 vaccination, MPLA-adjuvanted recombinant overlapping peptide E7 (ROP-E7) vaccination, anti-CD137 (4-1BB) agonism, and ROP-E7 plus anti-CD137 combination therapy. The study was designed to characterise treatment-associated changes in tumour immune and stromal transcriptional signatures.</description><dates><publication>2026/09/25</publication></dates><accession>GSE347031</accession><cross_references><GSM>GSM10044577</GSM><GSM>GSM10044576</GSM><GSM>GSM10044578</GSM><GSM>GSM10044573</GSM><GSM>GSM10044572</GSM><GSM>GSM10044575</GSM><GSM>GSM10044574</GSM><GSM>GSM10044571</GSM><GSM>GSM10044570</GSM><GSM>GSM10044569</GSM><GPL>24247</GPL><GSE>347031</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>