<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Appierdo R</submitter><funding>NIAMS NIH HHS</funding><pubmed_abstract>We performed a large-scale immunogenomic analysis of ~13,000 transcriptomic profiles from 10 autoimmune diseases, integrating publicly available datasets from both blood and tissue. Using meta-analysis, we identified core immune mechanisms underlying autoimmunity, including strong interferon responses, inflammation, and adaptive immune suppression, alongside disease-specific signatures. To enhance biological interpretability, we derived higher-order immune features - such as cell type proportions, cytokine levels, pathway activity, transcription factor regulation, and miRNA activity - and organized them into 15 coherent immune modules. These modules enabled systematic cross-disease comparisons, revealing shared and distinct immunopathological patterns. The inflammation module, in particula</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2025.09.12.675833</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12458282</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The Integrated Cellular and Molecular Landscape of Autoimmunity.</pubmed_title><pmcid>PMC12458282</pmcid><funding_grant_id>P30 AR070155</funding_grant_id><pubmed_authors>Appierdo R</pubmed_authors><pubmed_authors>Pepe G</pubmed_authors><pubmed_authors>Sirota M</pubmed_authors><pubmed_authors>Helmer-Citterich M</pubmed_authors><pubmed_authors>Gherardini PF</pubmed_authors><pubmed_authors>Vallania F</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Integrated Cellular and Molecular Landscape of Autoimmunity.</name><description>We performed a large-scale immunogenomic analysis of ~13,000 transcriptomic profiles from 10 autoimmune diseases, integrating publicly available datasets from both blood and tissue. Using meta-analysis, we identified core immune mechanisms underlying autoimmunity, including strong interferon responses, inflammation, and adaptive immune suppression, alongside disease-specific signatures. To enhance biological interpretability, we derived higher-order immune features - such as cell type proportions, cytokine levels, pathway activity, transcription factor regulation, and miRNA activity - and organized them into 15 coherent immune modules. These modules enabled systematic cross-disease comparisons, revealing shared and distinct immunopathological patterns. The inflammation module, in particula</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-05T03:13:22.045Z</modification><creation>2026-05-05T03:12:18.008Z</creation></dates><accession>S-EPMC12458282</accession><cross_references><pubmed>41000680</pubmed><doi>10.1101/2025.09.12.675833</doi></cross_references></HashMap>