<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Immormino RM</submitter><funding>The Arthur and Kayla Spector Charitable Fund</funding><funding>Thurston Arthritis Research Center</funding><funding>2020 American Association of Allergy, Asthma, and Immunology Foundation</funding><funding>NIH HHS</funding><pagination>vlaf008</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11893976</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(4)</volume><pubmed_abstract>Whether epigenetic factor UTX, a histone H3 lysine 27 (H3K27) demethylase, is critical for type 2 immunity, including allergic sensitization and antigen-driven anaphylaxis, is unclear. We used UTXfl/fl x Lck-Cre mice with UTX-deficient T cells (UTX-TCD) to determine whether T cell-specific UTX expression regulates antigen-specific IgE production after airway sensitization to peanut and anaphylaxis following intraperitoneal (i.p.) peanut challenge. UTX-TCD mice sensitized via the airway with peanut and lipopolysaccharide (LPS), a bacterial component and environmental adjuvant found in house dust, made 2-fold less peanut-IgE and 3.5-fold less peanut-IgG1 than comparably sensitized UTXfl/fl mice, despite higher total IgE and total IgG1 serum antibody levels pre-sensitization. Peanut-induced a</pubmed_abstract><journal>ImmunoHorizons</journal><pubmed_title>Deficiency of H3K27 histone demethylase UTX in T cells blunts allergic sensitization and anaphylaxis to peanut.</pubmed_title><pmcid>PMC11893976</pmcid><funding_grant_id>K08AI141691</funding_grant_id><funding_grant_id>R01 ES032544</funding_grant_id><pubmed_authors>Kulis MD</pubmed_authors><pubmed_authors>Iweala OI</pubmed_authors><pubmed_authors>Immormino RM</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Kesselring J</pubmed_authors><pubmed_authors>Carson AS</pubmed_authors><pubmed_authors>Kapita CM</pubmed_authors><pubmed_authors>Smeekens J</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Thomas KO</pubmed_authors><pubmed_authors>Moran TP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Deficiency of H3K27 histone demethylase UTX in T cells blunts allergic sensitization and anaphylaxis to peanut.</name><description>Whether epigenetic factor UTX, a histone H3 lysine 27 (H3K27) demethylase, is critical for type 2 immunity, including allergic sensitization and antigen-driven anaphylaxis, is unclear. We used UTXfl/fl x Lck-Cre mice with UTX-deficient T cells (UTX-TCD) to determine whether T cell-specific UTX expression regulates antigen-specific IgE production after airway sensitization to peanut and anaphylaxis following intraperitoneal (i.p.) peanut challenge. UTX-TCD mice sensitized via the airway with peanut and lipopolysaccharide (LPS), a bacterial component and environmental adjuvant found in house dust, made 2-fold less peanut-IgE and 3.5-fold less peanut-IgG1 than comparably sensitized UTXfl/fl mice, despite higher total IgE and total IgG1 serum antibody levels pre-sensitization. Peanut-induced a</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2025-04-06T22:38:10.514Z</modification><creation>2025-04-04T02:54:10.111Z</creation></dates><accession>S-EPMC11893976</accession><cross_references><pubmed>40065718</pubmed><doi>10.1093/immhor/vlaf008</doi></cross_references></HashMap>