<HashMap><database>GEO</database><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE291337</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Hijacking innate immunity to enhance mRNA therapeutics</name><description>The therapeutic success of in vitro-transcribed (IVT) mRNA depends on its stability and efficient translation. However, IVT mRNA is highly susceptible to immune-mediated degradation, limiting its efficacy. Here, we co-transfected IVT mCherry mRNA with immune suppressor M or SOCS1 mRNA in human umbilical vein endothelial cells (HUVECs) for 6h and 24h to explore whether hijacking innate immunity could enhance expression and half-life of IVT mRNA. Subsequently, RNA-seq was performed to investigate the transcriptomic changes in HUVECs after transfecting IVT mRNA. We sought to clarify the potential mechanism underlying degradation of IVT mRNA.</description><dates><publication>2026/03/25</publication></dates><accession>GSE291337</accession><cross_references><GSM>GSM8833649</GSM><GSM>GSM8833648</GSM><GSM>GSM8833647</GSM><GSM>GSM8833642</GSM><GSM>GSM8833663</GSM><GSM>GSM8833641</GSM><GSM>GSM8833640</GSM><GSM>GSM8833662</GSM><GSM>GSM8833661</GSM><GSM>GSM8833646</GSM><GSM>GSM8833645</GSM><GSM>GSM8833644</GSM><GSM>GSM8833643</GSM><GSM>GSM8833660</GSM><GSM>GSM8833639</GSM><GSM>GSM8833638</GSM><GSM>GSM8833637</GSM><GSM>GSM8833659</GSM><GSM>GSM8833658</GSM><GSM>GSM8833653</GSM><GSM>GSM8833652</GSM><GSM>GSM8833651</GSM><GSM>GSM8833650</GSM><GSM>GSM8833657</GSM><GSM>GSM8833656</GSM><GSM>GSM8833655</GSM><GSM>GSM8833654</GSM><GPL>24676</GPL><GSE>291337</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>