{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,20]],"date-time":"2026-10-20T18:45:36Z","timestamp":1792521936506,"version":"4.5.0"},"reference-count":58,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2026,6,12]],"date-time":"2026-06-12T00:00:00Z","timestamp":1781222400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Immunol."],"abstract":"<jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Rheumatoid arthritis-associated interstitial lung disease (RA-ILD) is a severe extra-articular manifestation with limited diagnostic biomarkers. While gut microbiota dysbiosis contributes to rheumatoid arthritis (RA) pathogenesis, its specific role in RA-ILD remains poorly characterized.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>We performed shotgun metagenomic sequencing on fecal samples from 41 participants: 10 RA-ILD patients, 20 RA patients without ILD (RA-non-ILD), and 11 healthy controls (HCs). We assessed alpha and beta diversity, differential abundance (Wilcoxon rank-sum tests with FDR correction), Spearman correlations with clinical parameters, microbial co-occurrence networks, and random forest classification.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Alpha and beta diversity did not differ significantly among groups. After FDR correction, no genus differed significantly between RA-ILD and RA-non-ILD. Exploratory analysis (uncorrected\n                      <jats:italic>P<\/jats:italic>\n                      \u00a0&amp;lt;\u00a00.05) revealed enrichment of\n                      <jats:italic>Escherichia\/Shigella<\/jats:italic>\n                      in RA-ILD (11.72% vs. 2.66%,\n                      <jats:italic>P<\/jats:italic>\n                      \u00a0=\u00a00.003) and depletion of\n                      <jats:italic>Roseburia<\/jats:italic>\n                      (1.05% vs. 3.77%,\n                      <jats:italic>P<\/jats:italic>\n                      \u00a0=\u00a00.005) and\n                      <jats:italic>Ruminococcus<\/jats:italic>\n                      (5.98% vs. 7.85%,\n                      <jats:italic>P<\/jats:italic>\n                      \u00a0=\u00a00.032), while\n                      <jats:italic>Faecalibacterium<\/jats:italic>\n                      showed a trend toward depletion without reaching nominal significance (4.45% vs. 4.66%,\n                      <jats:italic>P<\/jats:italic>\n                      \u00a0=\u00a00.409). Correlation analysis revealed a dichotomous pattern: pro-inflammatory genera correlated positively with disease activity, while butyrate-producing genera correlated negatively. Co-occurrence network analysis showed RA patients had a more complex network than HC and RA-ILD. Random forest classification identified\n                      <jats:italic>Bifidobacterium<\/jats:italic>\n                      , unclassified_ Oscillospiraceae, and unclassified_Lachnospiraceae as top discriminators between HC and RA, and unclassified_ Bacteroidaceae,\n                      <jats:italic>Parabacteroides<\/jats:italic>\n                      , and\n                      <jats:italic>Blautia<\/jats:italic>\n                      for RA-ILD vs RA.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      RA-ILD is associated with specific gut microbial alterations\u2014notably\u00a0\n                      <jats:italic>Escherichia\/Shigella<\/jats:italic>\n                      enrichment and depletion of\n                      <jats:italic>Roseburia<\/jats:italic>\n                      and\n                      <jats:italic>Ruminococcus<\/jats:italic>\n                      \u2014despite preserved overall diversity. These changes correlate with systemic inflammation and suggest a role for the gut microbiota in RA-ILD pathogenesis via the gut-lung axis. The identified taxa warrant validation as candidate biomarkers in larger cohorts.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.3389\/fimmu.2026.1868704","type":"journal-article","created":{"date-parts":[[2026,6,12]],"date-time":"2026-06-12T04:43:58Z","timestamp":1781239438000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":1,"title":["Metagenomic characterization of gut microbiota in rheumatoid arthritis-associated interstitial lung disease: taxonomic shifts and clinical correlations"],"prefix":"10.3389","volume":"17","author":[{"given":"Ran","family":"Fan","sequence":"first","affiliation":[{"name":"Department of Rheumatology and Immunology, Jiangsu Province (Suqian) Hospital","place":["Suqian, Jiangsu, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Qifeng","family":"Zang","sequence":"additional","affiliation":[{"name":"School of Life Sciences, Bengbu Medical 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