<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Schiller HB</submitter><funding>NHLBI NIH HHS</funding><pagination>1298-1310</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6913086</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>196(10)</volume><pubmed_abstract>&lt;h4>Rationale&lt;/h4>Analyzing the molecular heterogeneity of different forms of organ fibrosis may reveal common and specific factors and thus identify potential future therapeutic targets.&lt;h4>Objectives&lt;/h4>We sought to use proteome-wide profiling of human tissue fibrosis to (1) identify common and specific signatures across end-stage interstitial lung disease (ILD) cases, (2) characterize ILD subgroups in an unbiased fashion, and (3) identify common and specific features of lung and skin fibrosis.&lt;h4>Methods&lt;/h4>We collected samples of ILD tissue (n = 45) and healthy donor control samples (n = 10), as well as fibrotic skin lesions from localized scleroderma and uninvolved skin (n = 6). Samples were profiled by quantitative label-free mass spectrometry, Western blotting, or confocal imaging</pubmed_abstract><journal>American journal of respiratory and critical care medicine</journal><pubmed_title>Deep Proteome Profiling Reveals Common Prevalence of MZB1-Positive Plasma B Cells in Human Lung and Skin Fibrosis.</pubmed_title><pmcid>PMC6913086</pmcid><funding_grant_id>R01 HL097163</funding_grant_id><funding_grant_id>R33 HL120770</funding_grant_id><pubmed_authors>Schwartz DA</pubmed_authors><pubmed_authors>Preisendorfer S</pubmed_authors><pubmed_authors>Moinzadeh P</pubmed_authors><pubmed_authors>Krieg T</pubmed_authors><pubmed_authors>Staab-Weijnitz C</pubmed_authors><pubmed_authors>Eckes B</pubmed_authors><pubmed_authors>Leuschner G</pubmed_authors><pubmed_authors>Mann M</pubmed_authors><pubmed_authors>Hatz RA</pubmed_authors><pubmed_authors>Behr J</pubmed_authors><pubmed_authors>Schiller HB</pubmed_authors><pubmed_authors>Mayr CH</pubmed_authors><pubmed_authors>Strunz M</pubmed_authors><pubmed_authors>Eickelberg O</pubmed_authors></additional><is_claimable>false</is_claimable><name>Deep Proteome Profiling Reveals Common Prevalence of MZB1-Positive Plasma B Cells in Human Lung and Skin Fibrosis.</name><description>&lt;h4>Rationale&lt;/h4>Analyzing the molecular heterogeneity of different forms of organ fibrosis may reveal common and specific factors and thus identify potential future therapeutic targets.&lt;h4>Objectives&lt;/h4>We sought to use proteome-wide profiling of human tissue fibrosis to (1) identify common and specific signatures across end-stage interstitial lung disease (ILD) cases, (2) characterize ILD subgroups in an unbiased fashion, and (3) identify common and specific features of lung and skin fibrosis.&lt;h4>Methods&lt;/h4>We collected samples of ILD tissue (n = 45) and healthy donor control samples (n = 10), as well as fibrotic skin lesions from localized scleroderma and uninvolved skin (n = 6). Samples were profiled by quantitative label-free mass spectrometry, Western blotting, or confocal imaging</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Nov</publication><modification>2025-05-29T22:03:33.617Z</modification><creation>2025-05-29T22:03:33.617Z</creation></dates><accession>S-EPMC6913086</accession><cross_references><pubmed>28654764</pubmed><doi>10.1164/rccm.201611-2263OC</doi><doi>10.1164/rccm.201611-2263oc</doi></cross_references></HashMap>