<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Strohmeier V</submitter><funding>Bundesministerium für Bildung und Forschung</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>Universitätsklinikum Freiburg</funding><funding>Agentura Pro Zdravotnický Výzkum České Republiky</funding><funding>Fundação de Amparo à Pesquisa do Estado de São Paulo</funding><pagination>371-390</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9892141</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>43(2)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>About 15% of patients with common variable immunodeficiency (CVID) develop a small intestinal enteropathy, which resembles celiac disease with regard to histopathology but evolves from a distinct, poorly defined pathogenesis that has been linked in some cases to chronic norovirus (NV) infection. Interferon-driven inflammation is a prominent feature of CVID enteropathy, but it remains unknown how NV infection may contribute.&lt;h4>Methods&lt;/h4>Duodenal biopsies of CVID patients, stratified according to the presence of villous atrophy (VA), IgA plasma cells (PCs), and chronic NV infection, were investigated by flow cytometry, multi-epitope-ligand cartography, bulk RNA-sequencing, and RT-qPCR of genes of interest.&lt;h4>Results&lt;/h4>VA development was connected to the lack of intestin</pubmed_abstract><journal>Journal of clinical immunology</journal><pubmed_title>Interferon-Driven Immune Dysregulation in Common Variable Immunodeficiency-Associated Villous Atrophy and Norovirus Infection.</pubmed_title><pmcid>PMC9892141</pmcid><funding_grant_id>CIBSS–EXC-2189–Project ID 390939984</funding_grant_id><funding_grant_id>GAIN 748 01GM1910A</funding_grant_id><funding_grant_id>RESIST–EXC 2155–Project ID 517 390874280</funding_grant_id><funding_grant_id>SFB 1160 IMPATH project Z02N</funding_grant_id><funding_grant_id>NV18-05–00162</funding_grant_id><funding_grant_id>FAPESP grant 2020/01688-0</funding_grant_id><funding_grant_id>CRC1453 (Project ID 431984000 - S1)</funding_grant_id><funding_grant_id>SFB 1160 IMPATH project A04</funding_grant_id><funding_grant_id>SFB 1160 IMPATH project B05</funding_grant_id><funding_grant_id>CRC1479 (Project ID: 441891347- S1)</funding_grant_id><funding_grant_id>project Z01</funding_grant_id><funding_grant_id>Z1</funding_grant_id><funding_grant_id>CRC 850 subprojects C9</funding_grant_id><funding_grant_id>FKZ 01ZZ1801B</funding_grant_id><funding_grant_id>NU20-05–00282</funding_grant_id><funding_grant_id>GR1617/14-1/iPAD</funding_grant_id><funding_grant_id>SFB 1160 IMPATH project Z01</funding_grant_id><funding_grant_id>TRR167</funding_grant_id><pubmed_authors>Grimbacher B</pubmed_authors><pubmed_authors>Friedmann D</pubmed_authors><pubmed_authors>Bulashevska A</pubmed_authors><pubmed_authors>Eckert M</pubmed_authors><pubmed_authors>Gutenberger S</pubmed_authors><pubmed_authors>Schell C</pubmed_authors><pubmed_authors>Boerries M</pubmed_authors><pubmed_authors>Klocperk A</pubmed_authors><pubmed_authors>Seidl M</pubmed_authors><pubmed_authors>Grawe K</pubmed_authors><pubmed_authors>Shabani M</pubmed_authors><pubmed_authors>Pascual-Reguant A</pubmed_authors><pubmed_authors>Proietti M</pubmed_authors><pubmed_authors>Strohmeier V</pubmed_authors><pubmed_authors>Harder I</pubmed_authors><pubmed_authors>Hauser AE</pubmed_authors><pubmed_authors>Unger S</pubmed_authors><pubmed_authors>von Spee-Mayer C</pubmed_authors><pubmed_authors>Goldacker S</pubmed_authors><pubmed_authors>Warnatz K</pubmed_authors><pubmed_authors>Marques OC</pubmed_authors><pubmed_authors>Keller B</pubmed_authors><pubmed_authors>Provaznik J</pubmed_authors><pubmed_authors>Hasselblatt P</pubmed_authors><pubmed_authors>Andrieux G</pubmed_authors><pubmed_authors>Benes V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Interferon-Driven Immune Dysregulation in Common Variable Immunodeficiency-Associated Villous Atrophy and Norovirus Infection.</name><description>&lt;h4>Purpose&lt;/h4>About 15% of patients with common variable immunodeficiency (CVID) develop a small intestinal enteropathy, which resembles celiac disease with regard to histopathology but evolves from a distinct, poorly defined pathogenesis that has been linked in some cases to chronic norovirus (NV) infection. Interferon-driven inflammation is a prominent feature of CVID enteropathy, but it remains unknown how NV infection may contribute.&lt;h4>Methods&lt;/h4>Duodenal biopsies of CVID patients, stratified according to the presence of villous atrophy (VA), IgA plasma cells (PCs), and chronic NV infection, were investigated by flow cytometry, multi-epitope-ligand cartography, bulk RNA-sequencing, and RT-qPCR of genes of interest.&lt;h4>Results&lt;/h4>VA development was connected to the lack of intestin</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-07-16T20:12:18.623Z</modification><creation>2025-04-05T23:23:18.959Z</creation></dates><accession>S-EPMC9892141</accession><cross_references><pubmed>36282455</pubmed><doi>10.1007/s10875-022-01379-2</doi></cross_references></HashMap>