<HashMap><database>biostudies-literature</database><scores/><additional><submitter>De Maria R</submitter><funding>FPRC 5 per mille 2020 MUR</funding><funding>IRCC</funding><pagination>306</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12433426</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>74(10)</volume><pubmed_abstract>Advanced-stage sarcomas pose a major challenge in oncology, as they are often resistant to conventional therapies and associated with poor prognosis. CAR-based cellular immunotherapy is emerging as a very promising therapeutic option; however, clinically relevant animal models are urgently needed to accelerate the clinical development of these approaches. B7-H3 molecule, due to its low expression in normal tissue, high prevalence in multiple human cancers, and association with cancer stemness and aggressiveness, represents one of the most attractive targets for CAR-immunotherapy. In this study, we established a preclinical cellular immunotherapy platform based on canine cytokine-induced killer cells (CIK) redirected by an antihuman B7-H3 CAR against canine sarcoma cells and 3D sarcoma sphe</pubmed_abstract><journal>Cancer immunology, immunotherapy : CII</journal><pubmed_title>Development and activity of canine B7-H3-CAR.CIK lymphocytes against sarcomas: preclinical evidence and perspectives for human clinical translation.</pubmed_title><pmcid>PMC12433426</pmcid><funding_grant_id>Ricerca Corrente 2024</funding_grant_id><funding_grant_id>K9 HUMAN PROGRAM.</funding_grant_id><pubmed_authors>Landoni E</pubmed_authors><pubmed_authors>Aresu L</pubmed_authors><pubmed_authors>Capellero S</pubmed_authors><pubmed_authors>Vitali L</pubmed_authors><pubmed_authors>Sangiolo D</pubmed_authors><pubmed_authors>Berrino E</pubmed_authors><pubmed_authors>Leuci V</pubmed_authors><pubmed_authors>Grignani G</pubmed_authors><pubmed_authors>De Maria R</pubmed_authors><pubmed_authors>Vigna E</pubmed_authors><pubmed_authors>Dotti G</pubmed_authors><pubmed_authors>Sapino A</pubmed_authors><pubmed_authors>Olimpo M</pubmed_authors><pubmed_authors>Proment A</pubmed_authors><pubmed_authors>Donini C</pubmed_authors><pubmed_authors>Accornero P</pubmed_authors><pubmed_authors>Cesar Conti L</pubmed_authors><pubmed_authors>Massa A</pubmed_authors><pubmed_authors>Galvagno F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development and activity of canine B7-H3-CAR.CIK lymphocytes against sarcomas: preclinical evidence and perspectives for human clinical translation.</name><description>Advanced-stage sarcomas pose a major challenge in oncology, as they are often resistant to conventional therapies and associated with poor prognosis. CAR-based cellular immunotherapy is emerging as a very promising therapeutic option; however, clinically relevant animal models are urgently needed to accelerate the clinical development of these approaches. B7-H3 molecule, due to its low expression in normal tissue, high prevalence in multiple human cancers, and association with cancer stemness and aggressiveness, represents one of the most attractive targets for CAR-immunotherapy. In this study, we established a preclinical cellular immunotherapy platform based on canine cytokine-induced killer cells (CIK) redirected by an antihuman B7-H3 CAR against canine sarcoma cells and 3D sarcoma sphe</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-01T14:02:02.707Z</modification><creation>2026-04-08T13:19:03.718Z</creation></dates><accession>S-EPMC12433426</accession><cross_references><pubmed>40944715</pubmed><doi>10.1007/s00262-025-04163-4</doi></cross_references></HashMap>