<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/GSE299nnn/GSE299287/</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> Other</gds_type><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE299287</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>The effects of mIL-2/CD25 and anti-PD-1 mono- and combination therapies on the immune composition of the CT26 tumor microenvironment</name><description>Targeting IL-2 to CD8+ T cells expressing CD25 or PD-1 elicits optimal antitumor and antiviral CD8+ T cell responses. These effects are augmented when co-administered with PD-1/PD-L1 blockade. Here, we show that a mouse IL-2/CD25 fusion protein (mIL-2/CD25), which selectively targets CD25+ cells, promotes expansion of CD8+ T cells locally within CT26 tumors when administered at high doses (HD). However, tumor-associated CD25hi Tregs fail to expand and become unstable. Furthermore, in combination with PD-1 blockade, mIL-2/CD25 fusion protein-driven antitumor responses are enhanced and Treg migration is restricted to the tumor periphery. Single cell RNA sequencing (scRNA-seq) and TCR repertoire analysis show that hyperexpanded CD8+ T cells from mIL-2/CD25 fusion protein-treated mice exhibit high effector programming in a tumor antigen-specific manner. Expression of effector molecules was highest in CD8+ T cells generated by the combination of HD mIL-2/CD25 and anti-PD-1. Direct comparison of our scRNA-seq findings with that from an alternative approach, where IL-2 activity was targeted to PD-1+ CD8+ T cells using the PD1-IL2v fusion protein, reveals many similarities, but crucially, the combination of HD mIL-2/CD25 and anti-PD-1 is most effective at promoting effector function and “stem-like” CD8+ T cell subsets, suggesting this approach is superior. The differentiation of exhausted CD8+ T cells into highly functional cells and the potent antitumor responses by HD mIL-2/CD25 and anti-PD-1 raises the possibility that this combination approach may lead to greater response rates in patients than is achieved with either agent alone or with alternative IL-2 strategies.</description><dates><publication>2026/09/30</publication></dates><accession>GSE299287</accession><cross_references><GSM>GSM9036700</GSM><GSM>GSM9036701</GSM><GSM>GSM9036702</GSM><GSM>GSM9036703</GSM><GSM>GSM9036704</GSM><GSM>GSM9036705</GSM><GSM>GSM9036706</GSM><GSM>GSM9036707</GSM><GPL>24247</GPL><GSE>299287</GSE><taxon>Mus musculus</taxon><PMID>[42810810]</PMID></cross_references></HashMap>