<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9</volume><submitter>Chen PK</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>Neutralizing anti-interferon (IFN)-γ autoantibodies are linked to opportunistic infections (OIs). To explore the association between anti-IFN-γ autoantibodies and OIs in patients with adult-onset Still's disease (AOSD), we aimed to examine the ability of these autoantibodies to blockade signal transducer and activator of transcription (STAT1)-phosphorylation and chemokines production.&lt;h4>Methods&lt;/h4>Serum titers of anti-IFN-γ autoantibodies were quantified using ELISA in 29 AOSD and 22 healthy controls (HC). The detectable autoantibodies were verified with immunoblotting assay, and their neutralizing capacity against IFN-γ-signaling was evaluated with flow-cytometry analysis and immunoblotting. IFN-γ-mediated production of supernatant chemokines, including monocyte chemoa</pubmed_abstract><journal>Frontiers in medicine</journal><pagination>1097514</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9868624</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>High-titer anti-interferon-γ neutralizing autoantibodies linked to opportunistic infections in patients with adult-onset still's disease.</pubmed_title><pmcid>PMC9868624</pmcid><pubmed_authors>Chou CH</pubmed_authors><pubmed_authors>Chen PK</pubmed_authors><pubmed_authors>Chang SH</pubmed_authors><pubmed_authors>Chen DY</pubmed_authors><pubmed_authors>Liao TL</pubmed_authors><pubmed_authors>Yeo KJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>High-titer anti-interferon-γ neutralizing autoantibodies linked to opportunistic infections in patients with adult-onset still's disease.</name><description>&lt;h4>Objective&lt;/h4>Neutralizing anti-interferon (IFN)-γ autoantibodies are linked to opportunistic infections (OIs). To explore the association between anti-IFN-γ autoantibodies and OIs in patients with adult-onset Still's disease (AOSD), we aimed to examine the ability of these autoantibodies to blockade signal transducer and activator of transcription (STAT1)-phosphorylation and chemokines production.&lt;h4>Methods&lt;/h4>Serum titers of anti-IFN-γ autoantibodies were quantified using ELISA in 29 AOSD and 22 healthy controls (HC). The detectable autoantibodies were verified with immunoblotting assay, and their neutralizing capacity against IFN-γ-signaling was evaluated with flow-cytometry analysis and immunoblotting. IFN-γ-mediated production of supernatant chemokines, including monocyte chemoa</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T19:47:40.132Z</modification><creation>2025-04-04T19:47:40.132Z</creation></dates><accession>S-EPMC9868624</accession><cross_references><pubmed>36698819</pubmed><doi>10.3389/fmed.2022.1097514</doi></cross_references></HashMap>