<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jontvedt Jorgensen M</submitter><funding>Norges Forskningsråd</funding><funding>Helse Sør-Øst RHF</funding><pagination>669623</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8299478</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Eicosanoids and intracellular signaling pathways are potential targets for host-directed therapy (HDT) in tuberculosis (TB). We have explored the effect of cyclooxygenase 2 inhibitor (COX-2i) treatment on eicosanoid levels and signaling pathways in monocytes.&lt;h4>Methods&lt;/h4>Peripheral blood mononuclear cells isolated from TB patients included in a randomized phase I clinical trial of standard TB treatment with (n=21) or without (n=18) adjunctive COX-2i (etoricoxib) were analyzed at baseline, day 14 and day 56. Plasma eicosanoids were analyzed by ELISA and liquid chromatography-mass spectrometry (LC-MS), plasma cytokines by multiplex, and monocyte signaling by phospho-flow with a defined set of phospho-specific antibodies.&lt;h4>Results&lt;/h4>Lipoxygenase (LOX)-derived produ</pubmed_abstract><journal>Frontiers in cellular and infection microbiology</journal><pubmed_title>Plasma LOX-Products and Monocyte Signaling Is Reduced by Adjunctive Cyclooxygenase-2 Inhibitor in a Phase I Clinical Trial of Tuberculosis Patients.</pubmed_title><pmcid>PMC8299478</pmcid><funding_grant_id>GlobVac no 234493</funding_grant_id><pubmed_authors>Layre E</pubmed_authors><pubmed_authors>Aass HCD</pubmed_authors><pubmed_authors>Mortensen R</pubmed_authors><pubmed_authors>Tonby K</pubmed_authors><pubmed_authors>Jenum S</pubmed_authors><pubmed_authors>Tasken K</pubmed_authors><pubmed_authors>Dyrhol-Riise AM</pubmed_authors><pubmed_authors>Jontvedt Jorgensen M</pubmed_authors><pubmed_authors>Kvale D</pubmed_authors><pubmed_authors>Nore KG</pubmed_authors><pubmed_authors>Nigou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Plasma LOX-Products and Monocyte Signaling Is Reduced by Adjunctive Cyclooxygenase-2 Inhibitor in a Phase I Clinical Trial of Tuberculosis Patients.</name><description>&lt;h4>Introduction&lt;/h4>Eicosanoids and intracellular signaling pathways are potential targets for host-directed therapy (HDT) in tuberculosis (TB). We have explored the effect of cyclooxygenase 2 inhibitor (COX-2i) treatment on eicosanoid levels and signaling pathways in monocytes.&lt;h4>Methods&lt;/h4>Peripheral blood mononuclear cells isolated from TB patients included in a randomized phase I clinical trial of standard TB treatment with (n=21) or without (n=18) adjunctive COX-2i (etoricoxib) were analyzed at baseline, day 14 and day 56. Plasma eicosanoids were analyzed by ELISA and liquid chromatography-mass spectrometry (LC-MS), plasma cytokines by multiplex, and monocyte signaling by phospho-flow with a defined set of phospho-specific antibodies.&lt;h4>Results&lt;/h4>Lipoxygenase (LOX)-derived produ</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2026-05-08T18:49:37.048Z</modification><creation>2022-02-10T23:41:51.099Z</creation></dates><accession>S-EPMC8299478</accession><cross_references><pubmed>34307194</pubmed><doi>10.3389/fcimb.2021.669623</doi></cross_references></HashMap>