<HashMap><database>biostudies-other</database><scores/><additional><submitter>Le Floc'h A</submitter><pagination>559-570</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-ECPF-TABM-208</full_dataset_link><project>EurocanPlatform</project><project>EurocanPlatform core</project><abstract>The IGR-Heu tumor cell line was established from patient Heu suffering from large cell carcinoma of the lung. Heu171, Heu127 and Heu161 T cell clones were isolated from autologous tumor infiltrating lymphocytes. H32 T cell line and H32-22 clone were isolated from autologous PBL after stimulation with IGR-Heu and sorting with peptide-MHC tetramers. T cells were grown in the presence of irradiated autologous tumor and lymphoblastoid cell lines in complete media supplemented with rIL-2 and conditioned medium from phytohemagglutinin-activated lymphocytes for 3 weeks. Then, for microarray assays, RNA was extracted from the different cells.</abstract><repository>biostudies-other</repository><experiment_type>transcription profiling by array</experiment_type><data_source>EurocanPlatform</data_source><omics_type>Unknown</omics_type><volume>204</volume><journal>The Journal of experimental medicine</journal><species>Homo sapiens</species><pubmed_authors>Mami-Chouaib F</pubmed_authors><pubmed_authors>Le Floc'h A</pubmed_authors><pubmed_authors>Chouaib S</pubmed_authors><pubmed_authors>Lazar V</pubmed_authors><pubmed_authors>Bismuth G</pubmed_authors><pubmed_authors>Vergnon I</pubmed_authors><pubmed_authors>Jalil A</pubmed_authors><pubmed_authors>Le Maux Chansac B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcription profiling of human T cell lines isolated from tumor infiltrating lymphocytes or peripheral blood lymphocytes of a patient with large cell carcinoma of the lung</name><description>The IGR-Heu tumor cell line was established from patient Heu suffering from large cell carcinoma of the lung. Heu171, Heu127 and Heu161 T cell clones were isolated from autologous tumor infiltrating lymphocytes. H32 T cell line and H32-22 clone were isolated from autologous PBL after stimulation with IGR-Heu and sorting with peptide-MHC tetramers. T cells were grown in the presence of irradiated autologous tumor and lymphoblastoid cell lines in complete media supplemented with rIL-2 and conditioned medium from phytohemagglutinin-activated lymphocytes for 3 weeks. Then, for microarray assays, RNA was extracted from the different cells.</description><dates><release>2016-04-14T14:53:48Z</release><publication>2007 Mar</publication><modification>2016-04-14T14:53:48Z</modification><creation>2016-04-14T14:53:48Z</creation></dates><accession>S-ECPF-TABM-208</accession><cross_references><ArrayExpress>E-TABM-208</ArrayExpress><EFO>EFO_0003050</EFO><EFO>EFO_0000322</EFO><ArrayExpress files>E-TABM-208</ArrayExpress files></cross_references></HashMap>