<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(1)</volume><submitter>Choi H</submitter><pubmed_abstract>Adoptive transfer of γδ T cells is a novel immunotherapeutic approach to glioblastoma. Few recent studies have shown the efficacy of γδ T cells against glioblastoma, but no previous studies have identified the ligand-receptor interactions between γδ T cells and glioblastoma cells. Here, we identify those ligand-receptor interactions and provide a basis for using γδ T cells to treat glioblastoma. Vγ9Vδ2 T cells were generated from peripheral blood mononuclear cells of healthy donors using artificial antigen presenting cells. MICA, ULBP, PVR and Nectin-2 expression in 10 patient-derived glioblastoma (PDG) cells were analyzed. The in vitro cytokine secretion from the γδ T cells and their cytotoxicity toward the PDG cells were also analyzed. The in vivo anti-tumor effects were evaluated using </pubmed_abstract><journal>Oncoimmunology</journal><pagination>2138152</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9629076</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Human allogenic γδ T cells kill patient-derived glioblastoma cells expressing high levels of DNAM-1 ligands.</pubmed_title><pmcid>PMC9629076</pmcid><pubmed_authors>Kim TG</pubmed_authors><pubmed_authors>Park SA</pubmed_authors><pubmed_authors>Park J</pubmed_authors><pubmed_authors>Park JH</pubmed_authors><pubmed_authors>Choi H</pubmed_authors><pubmed_authors>Jeun SS</pubmed_authors><pubmed_authors>Lee HK</pubmed_authors><pubmed_authors>Lee Y</pubmed_authors><pubmed_authors>Ahn S</pubmed_authors><pubmed_authors>Lee JH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Human allogenic γδ T cells kill patient-derived glioblastoma cells expressing high levels of DNAM-1 ligands.</name><description>Adoptive transfer of γδ T cells is a novel immunotherapeutic approach to glioblastoma. Few recent studies have shown the efficacy of γδ T cells against glioblastoma, but no previous studies have identified the ligand-receptor interactions between γδ T cells and glioblastoma cells. Here, we identify those ligand-receptor interactions and provide a basis for using γδ T cells to treat glioblastoma. Vγ9Vδ2 T cells were generated from peripheral blood mononuclear cells of healthy donors using artificial antigen presenting cells. MICA, ULBP, PVR and Nectin-2 expression in 10 patient-derived glioblastoma (PDG) cells were analyzed. The in vitro cytokine secretion from the γδ T cells and their cytotoxicity toward the PDG cells were also analyzed. The in vivo anti-tumor effects were evaluated using </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-27T01:49:50.915Z</modification><creation>2025-04-06T18:20:50.527Z</creation></dates><accession>S-EPMC9629076</accession><cross_references><pubmed>36338147</pubmed><doi>10.1080/2162402X.2022.2138152</doi></cross_references></HashMap>