<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/GSE307nnn/GSE307999/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>Mus musculus</species><gds_type> Expression profiling by high throughput sequencing</gds_type><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE307999</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Single-cell RNA and TCR sequencing of tumor-infiltrating lymphocytes and draining lymph node immune cells following AMP-410 treatment</name><description>We employed single-cell RNA sequencing (scRNA-seq) and single-cell TCR sequencing (scTCR-seq) using the 10X Genomics platform to investigate immune cell dynamics during AMP-410 treatment in MC38 tumor-bearing b-h4-1BB transgenic mice. AMP-410 is a bifunctional VEGF-4-1BB biologic designed to simultaneously target VEGF and 4-1BB pathways, delivering a localized and synergistic approach to cancer immunotherapy. This study demonstrates that dual targeting of VEGF and 4-1BB signaling normalizes the tumor microenvironment, prevents T cell exhaustion in the TME in the later stage and also reduce the T cell conal exchange between tumor microenvironment and draining lymph nodes (dLNs), suggesting a local activity.</description><dates><publication>2026/09/10</publication></dates><accession>GSE307999</accession><cross_references><GSM>GSM9235386</GSM><GSM>GSM9235396</GSM><GSM>GSM9235385</GSM><GSM>GSM9235388</GSM><GSM>GSM9235387</GSM><GSM>GSM9235393</GSM><GSM>GSM9235392</GSM><GSM>GSM9235395</GSM><GSM>GSM9235394</GSM><GSM>GSM9235391</GSM><GSM>GSM9235390</GSM><GSM>GSM9235389</GSM><GPL>24247</GPL><GSE>307999</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>