{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,6]],"date-time":"2026-11-06T00:41:25Z","timestamp":1793925685700,"version":"4.8.0"},"reference-count":35,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2012,6,8]],"date-time":"2012-06-08T00:00:00Z","timestamp":1339113600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Allergy"],"published-print":{"date-parts":[[2012,7]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Chronic rhinosinusitis (<jats:styled-content style=\"fixed-case\">CRS<\/jats:styled-content>) is a disease characterized by inflammation of the nasal mucosa and paranasal sinuses. This inflammation may result in part from decreased epithelial barrier and innate immune responses, leading to frequent bacterial and fungal colonization. The objectives of this study were to investigate the expression of innate immune proteins of the palate lung and nasal epithelium clone (<jats:styled-content style=\"fixed-case\">PLUNC<\/jats:styled-content>) family in patients with <jats:styled-content style=\"fixed-case\">CRS<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Nasal tissue samples were collected from control subjects and <jats:styled-content style=\"fixed-case\">CRS<\/jats:styled-content> patients with and without nasal polyps. Expression of the members of the <jats:styled-content style=\"fixed-case\">PLUNC<\/jats:styled-content> family was analyzed by real\u2010time <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content>. Expression of <jats:styled-content style=\"fixed-case\">SPLUNC<\/jats:styled-content>1 and <jats:styled-content style=\"fixed-case\">LPLUNC<\/jats:styled-content>2 proteins was analyzed by <jats:styled-content style=\"fixed-case\">ELISA<\/jats:styled-content>, immunoblot, and immunohistochemical analysis.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Levels of <jats:styled-content style=\"fixed-case\">mRNA<\/jats:styled-content> for most of the members of the <jats:styled-content style=\"fixed-case\">PLUNC<\/jats:styled-content> family were profoundly reduced in nasal polyps (<jats:styled-content style=\"fixed-case\">NP<\/jats:styled-content>s) compared to uncinate tissue from control subjects or patients with <jats:styled-content style=\"fixed-case\">CRS<\/jats:styled-content>. <jats:styled-content style=\"fixed-case\">LPLUNC<\/jats:styled-content>2 and <jats:styled-content style=\"fixed-case\">SPLUNC<\/jats:styled-content>1 proteins were decreased in <jats:styled-content style=\"fixed-case\">NP<\/jats:styled-content>s of patients with <jats:styled-content style=\"fixed-case\">CRS<\/jats:styled-content> compared to uncinate tissue from control subjects. Immunohistochemical data revealed that within submucosal glands of sinonasal tissues, <jats:styled-content style=\"fixed-case\">SPLUNC<\/jats:styled-content>1 and <jats:styled-content style=\"fixed-case\">LPLUNC<\/jats:styled-content>2 were differentially expressed, in serous and mucous cells, respectively. The decrease in the expression of these molecules is probably explained by a decrease in the number of glands in <jats:styled-content style=\"fixed-case\">NP<\/jats:styled-content>s as revealed by correlations with levels of the glandular marker lactoferrin.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Decreased <jats:styled-content style=\"fixed-case\">SPLUNC<\/jats:styled-content>1 and <jats:styled-content style=\"fixed-case\">LPLUNC<\/jats:styled-content>2 in <jats:styled-content style=\"fixed-case\">NP<\/jats:styled-content>s reflect a profound decrease in the number of submucosal glands. Decreased glands may lead to a localized defect in the production and release of glandular innate defense molecules.<\/jats:p><\/jats:sec>","DOI":"10.1111\/j.1398-9995.2012.02848.x","type":"journal-article","created":{"date-parts":[[2012,6,8]],"date-time":"2012-06-08T10:54:31Z","timestamp":1339152871000},"page":"920-928","source":"Crossref","is-referenced-by-count":98,"title":["Reduced expression of antimicrobial <scp>PLUNC<\/scp> proteins in nasal polyp tissues of patients with chronic rhinosinusitis"],"prefix":"10.1111","volume":"67","author":[{"given":"S.","family":"Seshadri","sequence":"first","affiliation":[{"name":"Division of Allergy\u2010Immunology Department of Medicine Northwestern University Feinberg School of Medicine Chicago IL USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D. 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E.","family":"Norton","sequence":"additional","affiliation":[{"name":"Division of Allergy\u2010Immunology Department of Medicine Northwestern University Feinberg School of Medicine Chicago IL USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L.","family":"Suh","sequence":"additional","affiliation":[{"name":"Division of Allergy\u2010Immunology Department of Medicine Northwestern University Feinberg School of Medicine Chicago IL USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A.","family":"Kato","sequence":"additional","affiliation":[{"name":"Division of Allergy\u2010Immunology Department of Medicine Northwestern University Feinberg School of Medicine Chicago IL USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R. 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