<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>61(10)</volume><submitter>Winkler C</submitter><pubmed_abstract>Cytotoxic T lymphocytes (CTL) can kill Hodgkin's lymphoma (HL) cells, and CTL have been used for the treatment of Epstein-Barr virus (EBV)-positive HL. For patients with EBV-negative HL, this strategy cannot be employed and alternative target structures have to be defined. In order to establish a system for the stimulation of HL-reactive T cells, we used dendritic cells (DC) as antigen-presenting cells for autologous T cells and transfected these DC with RNA from established HL cell lines. After stimulation of peripheral blood mononuclear cells (PBMC) with RNA-transfected DC, we analyzed the reactivity of primed PBMC by interferon gamma enzyme-linked immunospot. Our results suggest the presence of antigens with expression in HL cell lines and recognition of these antigens in combination wi</pubmed_abstract><journal>Cancer immunology, immunotherapy : CII</journal><pagination>1769-79</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11029013</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Hodgkin's lymphoma RNA-transfected dendritic cells induce cancer/testis antigen-specific immune responses.</pubmed_title><pmcid>PMC11029013</pmcid><pubmed_authors>Schlaf G</pubmed_authors><pubmed_authors>Max D</pubmed_authors><pubmed_authors>Altermann W</pubmed_authors><pubmed_authors>Banning-Eichenseer U</pubmed_authors><pubmed_authors>Kewitz S</pubmed_authors><pubmed_authors>Kornhuber M</pubmed_authors><pubmed_authors>Staege MS</pubmed_authors><pubmed_authors>Steingrube DS</pubmed_authors><pubmed_authors>Emmer A</pubmed_authors><pubmed_authors>Winkler C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hodgkin's lymphoma RNA-transfected dendritic cells induce cancer/testis antigen-specific immune responses.</name><description>Cytotoxic T lymphocytes (CTL) can kill Hodgkin's lymphoma (HL) cells, and CTL have been used for the treatment of Epstein-Barr virus (EBV)-positive HL. For patients with EBV-negative HL, this strategy cannot be employed and alternative target structures have to be defined. In order to establish a system for the stimulation of HL-reactive T cells, we used dendritic cells (DC) as antigen-presenting cells for autologous T cells and transfected these DC with RNA from established HL cell lines. After stimulation of peripheral blood mononuclear cells (PBMC) with RNA-transfected DC, we analyzed the reactivity of primed PBMC by interferon gamma enzyme-linked immunospot. Our results suggest the presence of antigens with expression in HL cell lines and recognition of these antigens in combination wi</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Oct</publication><modification>2026-06-01T23:56:27.046Z</modification><creation>2026-05-24T03:07:36.012Z</creation></dates><accession>S-EPMC11029013</accession><cross_references><pubmed>22419371</pubmed><doi>10.1007/s00262-012-1239-z</doi></cross_references></HashMap>