<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Huang Y</submitter><pubmed_abstract>&lt;h4>Objectives&lt;/h4>To compare the proteomics of synovial fluid (SF)-derived exosomes in rheumatoid arthritis (RA), axial spondyloarthritis (axSpA), gout, and osteoarthritis (OA) patients.&lt;h4>Methods&lt;/h4>Exosomes were separated from SF by the Exoquick kit combined ultracentrifugation method. Tandem mass tags (TMT)-labeled liquid chromatography mass spectrometry (LC-MS/MS) technology was used to analyze the proteomics of SF-derived exosomes. Volcano plot, hierarchical cluster, gene ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were conducted.&lt;h4>Results&lt;/h4>A total of 1,678 credible proteins were detected. Sixty-nine differentially expressed proteins were found in gout, compared with OA, axSpA, and RA simultaneously. Twenty-five proteins were found highly</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>800902</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8961740</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>TMT-Based Quantitative Proteomics Analysis of Synovial Fluid-Derived Exosomes in Inflammatory Arthritis.</pubmed_title><pmcid>PMC8961740</pmcid><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Li T</pubmed_authors><pubmed_authors>Sun S</pubmed_authors><pubmed_authors>Huang X</pubmed_authors><pubmed_authors>Ji Z</pubmed_authors><pubmed_authors>Huang L</pubmed_authors><pubmed_authors>Huang Q</pubmed_authors><pubmed_authors>Deng W</pubmed_authors></additional><is_claimable>false</is_claimable><name>TMT-Based Quantitative Proteomics Analysis of Synovial Fluid-Derived Exosomes in Inflammatory Arthritis.</name><description>&lt;h4>Objectives&lt;/h4>To compare the proteomics of synovial fluid (SF)-derived exosomes in rheumatoid arthritis (RA), axial spondyloarthritis (axSpA), gout, and osteoarthritis (OA) patients.&lt;h4>Methods&lt;/h4>Exosomes were separated from SF by the Exoquick kit combined ultracentrifugation method. Tandem mass tags (TMT)-labeled liquid chromatography mass spectrometry (LC-MS/MS) technology was used to analyze the proteomics of SF-derived exosomes. Volcano plot, hierarchical cluster, gene ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were conducted.&lt;h4>Results&lt;/h4>A total of 1,678 credible proteins were detected. Sixty-nine differentially expressed proteins were found in gout, compared with OA, axSpA, and RA simultaneously. Twenty-five proteins were found highly</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-05T15:59:47.396Z</modification><creation>2025-04-05T15:59:47.396Z</creation></dates><accession>S-EPMC8961740</accession><cross_references><pubmed>35359923</pubmed><doi>10.3389/fimmu.2022.800902</doi></cross_references></HashMap>