<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/GSE307388/</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=GSE307388</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Immune checkpoint blockade augments lymphodepleting chemotherapy-induced antitumor immunity by expanding effector CD8+ T cell clones in preclinical models of cancer</name><description>Cancer treatment using immune checkpoint blockade (ICB) with anti-programmed cell death protein (PD)-1 and anti-cytotoxic T lymphocyte associated protein (CTLA)-4 has been successful. However, primary and acquired resistance limits clinical benefit. To improve the effectiveness of ICB therapies, strategies that reorchestrate anti-tumor immunity through mechanism-based drug combinations are being actively explored. The alkylating chemotherapeutic agent, cyclophosphamide (CTX), has direct tumoricidal and immunomodulatory properties, including the induction of homeostatic proliferation of T cells. Since ICB suppresses inhibitory signals in T cells, we hypothesized that ICB could augment CTX-induced homeostatic proliferation of antigen-specific T cells, thereby resetting the T cell receptor (TCR) repertoire in favor of tumor-specific T cells. Here, we show that a single dose of CTX one day prior to starting aPD-1+aCTLA-4 is sufficient to delay tumor progression in established melanoma and prolong survival in tumor-bearing mice in preclinical models. These effects extended to other lymphodepleting treatments, such as Gemcitabine and radiation therapy. The anti-tumor immune response was mainly driven by the clonal expansion of activated/effector CD8+ tumor infiltrating lymphocytes. Furthermore, combined CTX and aPD-1+aCTLA-4 treatment demonstrated efficacy across additional preclinical tumor models, including colorectal cancer and triple negative breast cancer. Overall, our findings highlight that the combination of CTX and aPD-1+aCTLA-4 represents a clinically relevant approach in the treatment of ICB-refractory tumors.</description><dates><publication>2026/06/10</publication></dates><accession>GSE307388</accession><cross_references><GSM>GSM9223199</GSM><GSM>GSM9223200</GSM><GSM>GSM9223198</GSM><GSM>GSM9223209</GSM><GSM>GSM9223207</GSM><GSM>GSM9223208</GSM><GSM>GSM9223205</GSM><GSM>GSM9223206</GSM><GSM>GSM9223203</GSM><GSM>GSM9223204</GSM><GSM>GSM9223201</GSM><GSM>GSM9223202</GSM><GPL>24247</GPL><GSE>307388</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>