<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE309nnn/GSE309936/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type> Other</gds_type><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE309936</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>mRNA expression profile of OVA-specific Th2 cells from cLNs of mice injected with or without OVA-specific IgE after nasal OVA challenge</name><description>To elucidate the role of systemic antigen-specific IgE in the local activation of Th2 cells during allergic rhinitis (AR), we employed an adoptive transfer-based AR mouse model. Mice were adoptively sensitized with OVA-specific IgE (OVA-IgE) and/or in vitro-differentiated OVA-specific Th2 (OVA-Th2) cells, followed by intranasal OVA challenge. Single-cell RNA sequencing was performed to analyze the mRNA expression profiles of Th2 cells isolated from cervical lymph nodes of mice injected with or without OVA-specific IgE. Freshly cultured OVA-Th2 cells were included as controls.</description><dates><publication>2026/05/24</publication></dates><accession>GSE309936</accession><cross_references><GSM>GSM9284994</GSM><GSM>GSM9284995</GSM><GPL>28457</GPL><GSE>309936</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>