<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/GSE334nnn/GSE334769/</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>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE334769</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Immunogen-Sponge Hydrogel Reverses TIM-3–Mediated Dendritic-Cell Exhaustion in Alveolar Echinococcosis</name><description>Alveolar echinococcosis (AE) induces profound dendritic-cell dysfunction characterized by elevated TIM-3 expression and impaired antigen presentation. To overcome parasite-induced immunosuppression, we developed a SHIFT-engineered Immunogen-Sponge hydrogel vaccine incorporating protoscolex-derived antigens (PSAs). Bone marrow-derived dendritic cells (BMDCs) were treated with saline, PSA, F127@PSA, or SHIFT-F127@PSA and subjected to transcriptome sequencing. Comparative transcriptomic analyses were performed to investigate dendritic-cell activation, antigen presentation, immune signaling pathways, and TIM-3-associated regulatory mechanisms.</description><dates><publication>2026/08/08</publication></dates><accession>GSE334769</accession><cross_references><GSM>GSM9796849</GSM><GSM>GSM9796848</GSM><GSM>GSM9796850</GSM><GSM>GSM9796843</GSM><GSM>GSM9796854</GSM><GSM>GSM9796853</GSM><GSM>GSM9796852</GSM><GSM>GSM9796851</GSM><GSM>GSM9796847</GSM><GSM>GSM9796846</GSM><GSM>GSM9796845</GSM><GSM>GSM9796844</GSM><GPL>28330</GPL><GSE>334769</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>