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Human ficolin (\n                      <jats:styled-content style=\"fixed-case\">FCN<\/jats:styled-content>\n                      )\u20102 (L\u2010ficolin,\n                      <jats:styled-content style=\"fixed-case\">P35<\/jats:styled-content>\n                      ) and its mouse homolog\n                      <jats:styled-content style=\"fixed-case\">FCN<\/jats:styled-content>\n                      \u2010A are one of the major pattern recognition molecules of plasma\/serum, acting as important initiators of the lectin complement system and playing important roles in immunity, including respiratory immunity. However, little is known about the role of\n                      <jats:styled-content style=\"fixed-case\">FCN<\/jats:styled-content>\n                      \u20102\/A in allergic asthma.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Serum\n                      <jats:styled-content style=\"fixed-case\">FCN<\/jats:styled-content>\n                      \u20102 and\n                      <jats:styled-content style=\"fixed-case\">IgE<\/jats:styled-content>\n                      levels in 90 allergic asthmatic patients and 48 healthy controls were measured by\n                      <jats:styled-content style=\"fixed-case\">ELISA<\/jats:styled-content>\n                      . Aeroallergen house dust mite (\n                      <jats:styled-content style=\"fixed-case\">HDM<\/jats:styled-content>\n                      )\u2010induced mouse model of asthma was generated in both wild type (\n                      <jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content>\n                      ) and\n                      <jats:styled-content style=\"fixed-case\">FCN<\/jats:styled-content>\n                      \u2010A knockout (\n                      <jats:styled-content style=\"fixed-case\">KO<\/jats:styled-content>\n                      ) mice. Mouse serum and bronchoalveolar lavage fluid (\n                      <jats:styled-content style=\"fixed-case\">BALF<\/jats:styled-content>\n                      )\n                      <jats:styled-content style=\"fixed-case\">IgE<\/jats:styled-content>\n                      levels, lung innate lymphoid cells (\n                      <jats:styled-content style=\"fixed-case\">ILC<\/jats:styled-content>\n                      )1\/2\/3, the expression of transcription factors\n                      <jats:styled-content style=\"fixed-case\">GATA3<\/jats:styled-content>\n                      , T\u2010bet, and\n                      <jats:styled-content style=\"fixed-case\">ROR\u03b3t<\/jats:styled-content>\n                      , and the concentrations of type 2 cytokines in serum and\n                      <jats:styled-content style=\"fixed-case\">BALF<\/jats:styled-content>\n                      were measured by\n                      <jats:styled-content style=\"fixed-case\">FCM<\/jats:styled-content>\n                      ,\n                      <jats:styled-content style=\"fixed-case\">RT<\/jats:styled-content>\n                      \u2010\n                      <jats:styled-content style=\"fixed-case\">qPCR<\/jats:styled-content>\n                      , Western blot, and\n                      <jats:styled-content style=\"fixed-case\">ELISA<\/jats:styled-content>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Serum\n                      <jats:styled-content style=\"fixed-case\">FCN<\/jats:styled-content>\n                      \u20102 concentrations in patients with allergic asthma were significantly lower than those in healthy controls. Similarly, lower serum and\n                      <jats:styled-content style=\"fixed-case\">BALF FCN<\/jats:styled-content>\n                      \u2010A concentrations were observed in\n                      <jats:styled-content style=\"fixed-case\">HDM<\/jats:styled-content>\n                      \u2010induced asthma mouse models compared to those of uninduced mice. In the asthma mouse model,\n                      <jats:styled-content style=\"fixed-case\">FCN<\/jats:styled-content>\n                      \u2010A\n                      <jats:styled-content style=\"fixed-case\">KO<\/jats:styled-content>\n                      asthmatic mice had higher levels of total\n                      <jats:styled-content style=\"fixed-case\">IgE<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">HDM<\/jats:styled-content>\n                      \u2010specific\n                      <jats:styled-content style=\"fixed-case\">IgE<\/jats:styled-content>\n                      (\n                      <jats:styled-content style=\"fixed-case\">sIgE<\/jats:styled-content>\n                      ), \u03b2\u2010hexosaminidase (\u03b2\u2010\n                      <jats:styled-content style=\"fixed-case\">HEX<\/jats:styled-content>\n                      ) and histamine secretion, as well as increased airway epithelial permeability with the release of\n                      <jats:styled-content style=\"fixed-case\">FITC<\/jats:styled-content>\n                      \u2010dextran in sera, inflammatory cell infiltration and eosinophil counts, and displayed more severe disease symptoms with histological damage compared to\n                      <jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content>\n                      asthmatic mice.\n                      <jats:styled-content style=\"fixed-case\">FCN<\/jats:styled-content>\n                      \u2010A\n                      <jats:styled-content style=\"fixed-case\">KO<\/jats:styled-content>\n                      asthmatic mice showed decreased T\u2010bet\n                      <jats:sup>+<\/jats:sup>\n                      <jats:styled-content style=\"fixed-case\">ILC1<\/jats:styled-content>\n                      and increased\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u20105\n                      <jats:sup>+<\/jats:sup>\n                      \/\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u201013\n                      <jats:sup>+<\/jats:sup>\n                      <jats:styled-content style=\"fixed-case\">ILC2<\/jats:styled-content>\n                      \/\n                      <jats:styled-content style=\"fixed-case\">ILC2<\/jats:styled-content>\n                      proportions, p\u2010\n                      <jats:styled-content style=\"fixed-case\">GATA3<\/jats:styled-content>\n                      expression, serum and\n                      <jats:styled-content style=\"fixed-case\">BALF<\/jats:styled-content>\n                      type 2 cytokines\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u20104,\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u20105, and\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u201013, Th17 cytokine\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u201017, and chemokines\n                      <jats:styled-content style=\"fixed-case\">CCL2<\/jats:styled-content>\n                      \/4 production. Importantly, the administration of exogenous\n                      <jats:styled-content style=\"fixed-case\">FCN<\/jats:styled-content>\n                      \u2010A protected against mouse allergic airway inflammation with decreased\n                      <jats:styled-content style=\"fixed-case\">ILC2<\/jats:styled-content>\n                      proportions and type 2 cytokines expression, serum total and allergen\u2010specific\n                      <jats:styled-content style=\"fixed-case\">IgE<\/jats:styled-content>\n                      production. These results suggest that\n                      <jats:styled-content style=\"fixed-case\">FCN<\/jats:styled-content>\n                      \u2010A suppresses both\n                      <jats:styled-content style=\"fixed-case\">ILC2<\/jats:styled-content>\n                      innate immunity and\n                      <jats:styled-content style=\"fixed-case\">IgE<\/jats:styled-content>\n                      \u2010mediated adaptive immunity during asthma.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      Our findings provide previously unreported evidence that\n                      <jats:styled-content style=\"fixed-case\">FCN<\/jats:styled-content>\n                      \u2010A protects against allergic asthma by suppressing lung\n                      <jats:styled-content style=\"fixed-case\">ILC2<\/jats:styled-content>\n    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