{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,17]],"date-time":"2026-09-17T00:09:31Z","timestamp":1789603771904,"version":"build-2803163510"},"reference-count":13,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2026,7,22]],"date-time":"2026-07-22T00:00:00Z","timestamp":1784678400000},"content-version":"vor","delay-in-days":21,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T00:00:00Z","timestamp":1782864000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Pediatric Allergy Immunology"],"published-print":{"date-parts":[[2026,7]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      The nasal microbiome's role in predicting sublingual immunotherapy (SLIT) efficacy in children with allergic rhinitis (AR) remains unclear.\n                      <jats:italic>Haemophilus<\/jats:italic>\n                      , a\n                      <jats:italic>Proteobacteria<\/jats:italic>\n                      genus linked to respiratory inflammation, is a promising candidate biomarker.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>\n                      To evaluate\n                      <jats:italic>Haemophilus<\/jats:italic>\n                      dynamics as a potential predictor of SLIT response in children with moderate\u2013severe AR.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      In this prospective cohort, 63 children with AR and 40 healthy controls (CG) were enrolled. AR patients were stratified by disease severity (mild [MAR] vs. moderate\u2013severe [MSAR]), with MSAR patients receiving 1\u2010year standardized house dust mite SLIT. Based on &gt;20% reduction in Total Nasal Symptom Score (TNSS), patients were classified as responders (RG,\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u200925) or non\u2010responders (NRG,\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u200915). Nasal microbiome was profiled via 16S rDNA sequencing.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Compared to CG, AR children showed increased alpha diversity (Chao1,\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u2009.05; Shannon,\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u2009.01) and enrichment of\n                      <jats:italic>Staphylococcus<\/jats:italic>\n                      . MSAR patients had significantly higher\n                      <jats:italic>Proteobacteria<\/jats:italic>\n                      abundance, particularly\n                      <jats:italic>Haemophilus<\/jats:italic>\n                      , compared to MAR (LDA score &gt;4,\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u2009.001). After SLIT, RG patients showed normalized microbial evenness (Pielou E index) to CG levels, driven by marked\n                      <jats:italic>Haemophilus<\/jats:italic>\n                      depletion (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u2009.001). In contrast, NRG patients maintained high\n                      <jats:italic>Haemophilus<\/jats:italic>\n                      abundance.\n                      <jats:italic>Haemophilus<\/jats:italic>\n                      and\n                      <jats:italic>Moraxella<\/jats:italic>\n                      showed strong positive correlation (\n                      <jats:italic>r<\/jats:italic>\n                      \u2009=\u2009.68,\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u2009.001), with both decreasing in RG post\u2010SLIT.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      Elevated nasal\n                      <jats:italic>Haemophilus<\/jats:italic>\n                      is associated with AR severity, and its depletion correlates with SLIT efficacy.\n                      <jats:italic>Haemophilus<\/jats:italic>\n                      may serve as a clinically actionable microbial biomarker for monitoring SLIT response in pediatric AR, offering a novel precision medicine approach to allergen immunotherapy.\n                    <\/jats:p>\n                    <jats:p>\n                      <jats:boxed-text content-type=\"graphic\" position=\"anchor\">\n                        <jats:graphic xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" mimetype=\"image\/png\" position=\"anchor\" specific-use=\"enlarged-web-image\" xlink:href=\"graphic\/pai70437-gra-0001-m.png\">\n                          <jats:alt-text>image<\/jats:alt-text>\n                        <\/jats:graphic>\n                      <\/jats:boxed-text>\n                    <\/jats:p>\n                  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