<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Manohar M</submitter><funding>Simons Foundation</funding><funding>NIAID NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>2809-2826</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8609920</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>76(9)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Multifood oral immunotherapy (mOIT) with adjunctive anti-IgE (omalizumab, XOLAIR&lt;sup>®&lt;/sup> ) treatment affords safe, effective, and rapid desensitization to multiple foods, although the specific immune mechanisms mediating this desensitization remain to be fully elucidated.&lt;h4>Methods&lt;/h4>Participants in our phase 2 mOIT trial (NCT02643862) received omalizumab from baseline to week 16 and mOIT from week 8 to week 36. We compared the immune profile of PBMCs and plasma taken at baseline, week 8, and week 36 using high-dimensional mass cytometry, component-resolved diagnostics, the indirect basophil activation test, and Luminex.&lt;h4>Results&lt;/h4>We found (i) decreased frequency of IL-4&lt;sup>+&lt;/sup> peanut-reactive CD4&lt;sup>+&lt;/sup> T cells and a marked downregulation of GPR15 </pubmed_abstract><journal>Allergy</journal><pubmed_title>Immune changes beyond Th2 pathways during rapid multifood immunotherapy enabled with omalizumab.</pubmed_title><pmcid>PMC8609920</pmcid><funding_grant_id>U19AI104209</funding_grant_id><funding_grant_id>5UM2AI130836‐04</funding_grant_id><funding_grant_id>U19 AI104209</funding_grant_id><funding_grant_id>U01 AI140498</funding_grant_id><funding_grant_id>R01AI140134-02</funding_grant_id><funding_grant_id>T32 AI007512</funding_grant_id><funding_grant_id>5T32AI007512</funding_grant_id><funding_grant_id>R01AI140134‐02</funding_grant_id><funding_grant_id>U01 AI140498-03</funding_grant_id><funding_grant_id>U01 AI147462</funding_grant_id><funding_grant_id>5UM2AI130836-04</funding_grant_id><funding_grant_id>R01 AI140134</funding_grant_id><funding_grant_id>U01 AI140498‐03</funding_grant_id><funding_grant_id>UM2 AI130836</funding_grant_id><funding_grant_id>R01AI119918</funding_grant_id><funding_grant_id>R01 AI119918</funding_grant_id><pubmed_authors>DeKruyff RH</pubmed_authors><pubmed_authors>Gupta S</pubmed_authors><pubmed_authors>Desai M</pubmed_authors><pubmed_authors>Boyd SD</pubmed_authors><pubmed_authors>Oettgen HC</pubmed_authors><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Andorf S</pubmed_authors><pubmed_authors>Nadeau KC</pubmed_authors><pubmed_authors>Roy Chowdhury R</pubmed_authors><pubmed_authors>Yan Z</pubmed_authors><pubmed_authors>Minnicozzi S</pubmed_authors><pubmed_authors>Kost LE</pubmed_authors><pubmed_authors>Galli SJ</pubmed_authors><pubmed_authors>Manohar M</pubmed_authors><pubmed_authors>Maecker HT</pubmed_authors><pubmed_authors>Yu W</pubmed_authors><pubmed_authors>Kirkey M</pubmed_authors><pubmed_authors>Bunning B</pubmed_authors><pubmed_authors>Chinthrajah RS</pubmed_authors><pubmed_authors>Dunham D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immune changes beyond Th2 pathways during rapid multifood immunotherapy enabled with omalizumab.</name><description>&lt;h4>Background&lt;/h4>Multifood oral immunotherapy (mOIT) with adjunctive anti-IgE (omalizumab, XOLAIR&lt;sup>®&lt;/sup> ) treatment affords safe, effective, and rapid desensitization to multiple foods, although the specific immune mechanisms mediating this desensitization remain to be fully elucidated.&lt;h4>Methods&lt;/h4>Participants in our phase 2 mOIT trial (NCT02643862) received omalizumab from baseline to week 16 and mOIT from week 8 to week 36. We compared the immune profile of PBMCs and plasma taken at baseline, week 8, and week 36 using high-dimensional mass cytometry, component-resolved diagnostics, the indirect basophil activation test, and Luminex.&lt;h4>Results&lt;/h4>We found (i) decreased frequency of IL-4&lt;sup>+&lt;/sup> peanut-reactive CD4&lt;sup>+&lt;/sup> T cells and a marked downregulation of GPR15 </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2026-05-08T01:54:29.503Z</modification><creation>2024-11-20T11:17:59.577Z</creation></dates><accession>S-EPMC8609920</accession><cross_references><pubmed>33782956</pubmed><doi>10.1111/all.14833</doi></cross_references></HashMap>