<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><omics_type>Multiomics</omics_type><center_name>UCLA</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA85029</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>Leprosy presents as a clinical and immunological spectrum of disease. With the use of gene expression profiling, we observed that a distinction in gene expression correlates with and accurately classifies the clinical form of the disease. Genes belonging to the leukocyte immunoglobulin-like receptor (LIR) family were significantly up-regulated in lesions of lepromatous patients suffering from the disseminated form of the infection. In functional studies, LIR-7 suppressed innate host defense mechanisms by shifting monocyte production from interleukin-12 toward interleukin-10 and by blocking antimicrobial activity triggered by Toll-like receptors. Gene expression profiles may be useful in defining clinical forms of disease and providing insights into the regulation of immune responses to pathogens. Keywords: other</long_description><tag>xref:PubMed:12970564</tag><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Homo sapiens</name><description>Leprosy lesion gene expression</description><dates><last_updated>2025-09-24</last_updated><first_public>2014-02-11</first_public></dates><accession>PRJNA85029</accession><cross_references><GEO>GSE443</GEO><taxon>9606</taxon><PubMed>12970564</PubMed></cross_references></HashMap>