<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Alexandre M</submitter><pubmed_abstract>The role of IgE autoantibodies has been demonstrated in the pathogenesis of bullous pemphigoid for many years. Recently, omalizumab (OMZ), a humanized monoclonal anti-IgE antibody that depletes total serum IgE, has been used off-label in a few case series of bullous pemphigoids demonstrating a rapid efficacy and allowing significant improvements or complete remission as add-on therapy in first-line treatment-resistant patients. Herein, we report the largest retrospective study to evaluate OMZ effectiveness in patients with subepidermal autoimmune blistering diseases. Our series included 13 patients from a single center with bullous pemphigoid or mucous membrane pemphigoid, of whom 7 had mucous membrane involvement. OMZ was added to the unchanged immunosuppressive therapies. Detailed clinic</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>874108</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9065717</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Rapid Disease Control in First-Line Therapy-Resistant Mucous Membrane Pemphigoid and Bullous Pemphigoid with Omalizumab as Add-On Therapy: A Case Series Of 13 Patients.</pubmed_title><pmcid>PMC9065717</pmcid><pubmed_authors>Caux F</pubmed_authors><pubmed_authors>Prost-Squarcioni C</pubmed_authors><pubmed_authors>Alexandre M</pubmed_authors><pubmed_authors>Grootenboer-Mignot S</pubmed_authors><pubmed_authors>Bohelay G</pubmed_authors><pubmed_authors>Le Roux-Villet C</pubmed_authors><pubmed_authors>Morin F</pubmed_authors><pubmed_authors>Gille T</pubmed_authors><pubmed_authors>Soued I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rapid Disease Control in First-Line Therapy-Resistant Mucous Membrane Pemphigoid and Bullous Pemphigoid with Omalizumab as Add-On Therapy: A Case Series Of 13 Patients.</name><description>The role of IgE autoantibodies has been demonstrated in the pathogenesis of bullous pemphigoid for many years. Recently, omalizumab (OMZ), a humanized monoclonal anti-IgE antibody that depletes total serum IgE, has been used off-label in a few case series of bullous pemphigoids demonstrating a rapid efficacy and allowing significant improvements or complete remission as add-on therapy in first-line treatment-resistant patients. Herein, we report the largest retrospective study to evaluate OMZ effectiveness in patients with subepidermal autoimmune blistering diseases. Our series included 13 patients from a single center with bullous pemphigoid or mucous membrane pemphigoid, of whom 7 had mucous membrane involvement. OMZ was added to the unchanged immunosuppressive therapies. Detailed clinic</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T09:10:17.649Z</modification><creation>2025-04-04T09:10:17.649Z</creation></dates><accession>S-EPMC9065717</accession><cross_references><pubmed>35514989</pubmed><doi>10.3389/fimmu.2022.874108</doi></cross_references></HashMap>