<HashMap><database>bioimages</database><scores/><additional><omics_type>Unknown</omics_type><submitter>David Constant</submitter><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-BIAD3732</full_dataset_link><repository>bioimages</repository><figure_sub>Specimen</figure_sub><figure_sub>Image analysis</figure_sub><figure_sub>Funding</figure_sub><figure_sub>Study Component</figure_sub><figure_sub>Biosample</figure_sub><figure_sub>organisation</figure_sub><figure_sub>Associations</figure_sub><figure_sub>Image acquisition</figure_sub><pubmed_authors>Timothy Nice</pubmed_authors><pubmed_authors>David Constant</pubmed_authors></additional><is_claimable>false</is_claimable><name>Intestinal plasmacytoid dendritic cells preferentially produce interferon lambda contributing to localized innate immune responses</name><description>The healthy intestine maintains homeostasis in part via immune responses to microbiota, which includes basal production of interferon cytokines. Previous work showed that Type III Interferon (IFN-λ) stimulates localized pockets of interferon-stimulated genes (ISGs) in the adult mouse intestinal epithelium at homeostasis that provide preemptive protection from viral pathogens. Here, we demonstrate that a major source of homeostatic IFN-λ production in the intestine is a population of epithelium-associated plasmacytoid dendritic cells (pDC). Expansion of the pDC population increases epithelial ISG expression at homeostasis, suggesting the abundance of these cells is a limiting factor in IFN-λ responses. On the other hand, depletion of pDC or bone marrow reconstitution with IFN-λ-deficient pD</description><dates><release>2026-08-14T00:00:00Z</release><modification>2026-08-14T01:00:49.321Z</modification><creation>2026-08-03T17:26:25.328Z</creation></dates><accession>S-BIAD3732</accession><cross_references/></HashMap>