<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(1)</volume><submitter>Campo I</submitter><funding>Boehringer Ingelheim</funding><pubmed_abstract>Autoimmune pulmonary alveolar proteinosis (aPAP) is a rare lung disorder involving production of autoantibodies against endogenous granulocyte-macrophage colony-stimulating factor (GM-CSF). This study aimed to identify biomarkers that could be used to monitor for aPAP, particularly in patients treated with anti-GM-CSF antibodies. This was an exploratory, prospective, observational, single-center study. Pre-specified biomarkers were evaluated between baseline and Day 120 in serum/plasma, whole blood, sputum and exhaled breath condensate from patients with aPAP, healthy volunteers, and patients with chronic obstructive pulmonary disease (COPD) and asthma (not treated with anti-GM-CSF and with no evidence of aPAP). Pulmonary function tests were also performed. Overall, 144 individuals were en</pubmed_abstract><journal>Scientific reports</journal><pagination>8708</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9130212</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>An exploratory study investigating biomarkers associated with autoimmune pulmonary alveolar proteinosis (aPAP).</pubmed_title><pmcid>PMC9130212</pmcid><pubmed_authors>Gupta A</pubmed_authors><pubmed_authors>Gahlemann M</pubmed_authors><pubmed_authors>Ittrich C</pubmed_authors><pubmed_authors>Sauter W</pubmed_authors><pubmed_authors>Trapnell BC</pubmed_authors><pubmed_authors>Meloni F</pubmed_authors><pubmed_authors>Schoelch C</pubmed_authors><pubmed_authors>Campo I</pubmed_authors></additional><is_claimable>false</is_claimable><name>An exploratory study investigating biomarkers associated with autoimmune pulmonary alveolar proteinosis (aPAP).</name><description>Autoimmune pulmonary alveolar proteinosis (aPAP) is a rare lung disorder involving production of autoantibodies against endogenous granulocyte-macrophage colony-stimulating factor (GM-CSF). This study aimed to identify biomarkers that could be used to monitor for aPAP, particularly in patients treated with anti-GM-CSF antibodies. This was an exploratory, prospective, observational, single-center study. Pre-specified biomarkers were evaluated between baseline and Day 120 in serum/plasma, whole blood, sputum and exhaled breath condensate from patients with aPAP, healthy volunteers, and patients with chronic obstructive pulmonary disease (COPD) and asthma (not treated with anti-GM-CSF and with no evidence of aPAP). Pulmonary function tests were also performed. Overall, 144 individuals were en</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2026-05-09T18:56:20.475Z</modification><creation>2025-04-05T20:39:51.993Z</creation></dates><accession>S-EPMC9130212</accession><cross_references><pubmed>35610268</pubmed><doi>10.1038/s41598-022-11446-8</doi></cross_references></HashMap>