<HashMap><database>GEO</database><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE331111</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Expression data from OT-I CD8 T cells that are either naïve or isolated on day 5 following immunization with DC-OVA or with DC-OVA + LCMV</name><description>Inflamatory cytokines have a number of effects on the differentiation and function of CD8 T cells. To separate the effects of TCR/co-stimulation from the effects of inflammatory cytokines, we took an immunization approach. We transferred 1 x 10^4 OT-I CD8 T cells to naive C57BL/6 mice on day -1. On day 0 mice were immunized with either 5 x 10^5 OVA peptide loaded, LPS-matured dendritic cells (DC-OVA) injected ip or 5 x 10^5 DC-OVA and 2 x 10^5 pfu of LCMV injected ip. On day 5 following the indicated treatment, OT-I CD8 T cells were enriched via AutoMACS and sorted via flow cytometry prior to RNA extraction from 1 x 10^6 cells using an RNeasy kit (Qiagen). Naive OT-I CD8 T cells were enriched and sorted for RNA extraction to serve as a control. Each group had 3 biological replicates.</description><dates><publication>2026/06/01</publication></dates><accession>GSE331111</accession><cross_references><GSM>GSM9739179</GSM><GSM>GSM9739178</GSM><GSM>GSM9739177</GSM><GSM>GSM9739176</GSM><GSM>GSM9739184</GSM><GSM>GSM9739183</GSM><GSM>GSM9739182</GSM><GSM>GSM9739181</GSM><GSM>GSM9739180</GSM><GPL>6096</GPL><GSE>331111</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>