<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Webb ER</submitter><funding>Cancer Research UK</funding><pagination>104995</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9463572</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>25(9)</volume><pubmed_abstract>The outcome for children with high-risk neuroblastoma is poor despite intensive multi-modal treatment protocols. Toxicity from current treatments is significant, and novel approaches are needed to improve outcome. Cyclophosphamide (CPM) is a key component of current chemotherapy regimens and is known to have immunomodulatory effects. However, this has not been investigated in the context of tumor infiltrating lymphocytes in neuroblastoma. Using murine models of neuroblastoma, the immunomodulatory effects of low-dose CPM were investigated using detailed immunophenotyping. We demonstrated that CPM resulted in a specific depletion of intratumoral T regulatory cells by apoptosis, and when combined with anti-PD-1 antibody therapy, this resulted in improved therapeutic efficacy. CPM combined wit</pubmed_abstract><journal>iScience</journal><pubmed_title>Cyclophosphamide depletes tumor infiltrating T regulatory cells and combined with anti-PD-1 therapy improves survival in murine neuroblastoma.</pubmed_title><pmcid>PMC9463572</pmcid><funding_grant_id>20537</funding_grant_id><pubmed_authors>James S</pubmed_authors><pubmed_authors>Webb ER</pubmed_authors><pubmed_authors>Gray JC</pubmed_authors><pubmed_authors>Lanati S</pubmed_authors><pubmed_authors>Williams EL</pubmed_authors><pubmed_authors>Moreno-Vincente J</pubmed_authors><pubmed_authors>English V</pubmed_authors><pubmed_authors>Easton A</pubmed_authors><pubmed_authors>Beers SA</pubmed_authors><pubmed_authors>Penfold C</pubmed_authors><pubmed_authors>Taylor M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cyclophosphamide depletes tumor infiltrating T regulatory cells and combined with anti-PD-1 therapy improves survival in murine neuroblastoma.</name><description>The outcome for children with high-risk neuroblastoma is poor despite intensive multi-modal treatment protocols. Toxicity from current treatments is significant, and novel approaches are needed to improve outcome. Cyclophosphamide (CPM) is a key component of current chemotherapy regimens and is known to have immunomodulatory effects. However, this has not been investigated in the context of tumor infiltrating lymphocytes in neuroblastoma. Using murine models of neuroblastoma, the immunomodulatory effects of low-dose CPM were investigated using detailed immunophenotyping. We demonstrated that CPM resulted in a specific depletion of intratumoral T regulatory cells by apoptosis, and when combined with anti-PD-1 antibody therapy, this resulted in improved therapeutic efficacy. CPM combined wit</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2026-05-28T03:18:24.279Z</modification><creation>2025-04-07T08:29:22.91Z</creation></dates><accession>S-EPMC9463572</accession><cross_references><pubmed>36097618</pubmed><doi>10.1016/j.isci.2022.104995</doi></cross_references></HashMap>