<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Saper VE</submitter><funding>Arthritis Foundation</funding><funding>Intramural NIH HHS</funding><funding>NIAMS</funding><funding>Eunice Kennedy Shriver National Institute of Child Health and Human Development</funding><funding>NICHD NIH HHS</funding><funding>Rheumatology Research Foundation</funding><funding>Childhood Arthritis and Rheumatology Research Alliance</funding><funding>National Institutes of Health</funding><funding>National Institute of General Medical Sciences</funding><funding>Fonds Wetenschappelijk Onderzoek</funding><funding>NIAMS NIH HHS</funding><funding>David and Lucile Packard Foundation</funding><funding>NIGMS NIH HHS</funding><funding>Lucile Packard Foundation for Children&amp;apos;s Health</funding><pagination>2996-3013.e7</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11560592</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(11)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>After introducing IL-1/IL-6 inhibitors, some patients with Still and Still-like disease developed unusual, often fatal, pulmonary disease. This complication was associated with scoring as DReSS (drug reaction with eosinophilia and systemic symptoms) implicating these inhibitors, although DReSS can be difficult to recognize in the setting of systemic inflammatory disease.&lt;h4>Objective&lt;/h4>To facilitate recognition of IL-1/IL-6 inhibitor-DReSS in systemic inflammatory illnesses (Still/Still-like) by looking at timing and reaction-associated features. We evaluated outcomes of stopping or not stopping IL-1/IL-6 inhibitors after DReSS reaction began.&lt;h4>Methods&lt;/h4>In an international study collaborating primarily with pediatric specialists, we characterized features of 89 dr</pubmed_abstract><journal>The journal of allergy and clinical immunology. In practice</journal><pubmed_title>Interleukin (IL)-1/IL-6-Inhibitor-Associated Drug Reaction With Eosinophilia and Systemic Symptoms (DReSS) in Systemic Inflammatory Illnesses.</pubmed_title><pmcid>PMC11560592</pmcid><funding_grant_id>Z01AR041198</funding_grant_id><funding_grant_id>ZIA AR041198</funding_grant_id><funding_grant_id>T32HD104576</funding_grant_id><funding_grant_id>T32 HD104576</funding_grant_id><funding_grant_id>T32 AR050942</funding_grant_id><funding_grant_id>T32GM086330</funding_grant_id><funding_grant_id>T32 GM086330</funding_grant_id><pubmed_authors>Aviran Dagan N</pubmed_authors><pubmed_authors>Taneja A</pubmed_authors><pubmed_authors>Orandi A</pubmed_authors><pubmed_authors>Shehab A</pubmed_authors><pubmed_authors>Rafko J</pubmed_authors><pubmed_authors>Ruth N</pubmed_authors><pubmed_authors>Edelheit BS</pubmed_authors><pubmed_authors>Dalrymple A</pubmed_authors><pubmed_authors>Riordan M</pubmed_authors><pubmed_authors>Woolnough 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CK</pubmed_authors><pubmed_authors>Baluta S</pubmed_authors><pubmed_authors>Graham T</pubmed_authors><pubmed_authors>Berard RA</pubmed_authors><pubmed_authors>Wagner-Weiner L</pubmed_authors><pubmed_authors>Perfetto J</pubmed_authors><pubmed_authors>Balboni I</pubmed_authors><pubmed_authors>Sarkissian A</pubmed_authors><pubmed_authors>Yalcindag A</pubmed_authors><pubmed_authors>Kaidar K</pubmed_authors><pubmed_authors>Long A</pubmed_authors><pubmed_authors>Alvarez MB</pubmed_authors><pubmed_authors>Tsin CM</pubmed_authors><pubmed_authors>Lawson EF</pubmed_authors><pubmed_authors>Imlay A</pubmed_authors><pubmed_authors>Durkee D</pubmed_authors><pubmed_authors>Elzaki Y</pubmed_authors><pubmed_authors>Dhanrajani A</pubmed_authors><pubmed_authors>Torok K</pubmed_authors><pubmed_authors>Datyner E</pubmed_authors><pubmed_authors>Gironella A</pubmed_authors><pubmed_authors>Schultz K</pubmed_authors><pubmed_authors>Rogers D</pubmed_authors><pubmed_authors>Alperin R</pubmed_authors><pubmed_authors>Randell R</pubmed_authors><pubmed_authors>Sterba Rakovchik Y</pubmed_authors><pubmed_authors>Gorry S</pubmed_authors><pubmed_authors>Delnay N</pubmed_authors><pubmed_authors>Robinson L</pubmed_authors><pubmed_authors>Morgan E</pubmed_authors><pubmed_authors>Sheets R</pubmed_authors><pubmed_authors>Mellins ED</pubmed_authors><pubmed_authors>Ramanan AV</pubmed_authors><pubmed_authors>Schmitt E</pubmed_authors><pubmed_authors>Robinson A</pubmed_authors><pubmed_authors>Kovalick L</pubmed_authors><pubmed_authors>Nguyen A</pubmed_authors><pubmed_authors>Fuller J</pubmed_authors><pubmed_authors>Shishov M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Interleukin (IL)-1/IL-6-Inhibitor-Associated Drug Reaction With Eosinophilia and Systemic Symptoms (DReSS) in Systemic Inflammatory Illnesses.</name><description>&lt;h4>Background&lt;/h4>After introducing IL-1/IL-6 inhibitors, some patients with Still and Still-like disease developed unusual, often fatal, pulmonary disease. This complication was associated with scoring as DReSS (drug reaction with eosinophilia and systemic symptoms) implicating these inhibitors, although DReSS can be difficult to recognize in the setting of systemic inflammatory disease.&lt;h4>Objective&lt;/h4>To facilitate recognition of IL-1/IL-6 inhibitor-DReSS in systemic inflammatory illnesses (Still/Still-like) by looking at timing and reaction-associated features. We evaluated outcomes of stopping or not stopping IL-1/IL-6 inhibitors after DReSS reaction began.&lt;h4>Methods&lt;/h4>In an international study collaborating primarily with pediatric specialists, we characterized features of 89 dr</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-06-05T07:28:03.174Z</modification><creation>2026-05-14T03:12:44.125Z</creation></dates><accession>S-EPMC11560592</accession><cross_references><pubmed>39002722</pubmed><doi>10.1016/j.jaip.2024.07.002</doi></cross_references></HashMap>