{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,29]],"date-time":"2026-04-29T01:38:59Z","timestamp":1777426739961,"version":"3.51.4"},"reference-count":37,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2007,10,5]],"date-time":"2007-10-05T00:00:00Z","timestamp":1191542400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Experimental Dermatology"],"published-print":{"date-parts":[[2008,1]]},"abstract":"<jats:p><jats:bold>Abstract:\u2002<\/jats:bold> Pemphigus vulgaris (PV) is associated with autoantibodies against desmoglein (Dsg) 3 inducing epidermal loss of adhesion. The major pathogenic epitopes of Dsg3 are presumably dependent of their conformation. The aim of this study was to characterize the IgG reactivity of sera from a cohort of clinically well\u2010characterized PV patients against presumably non\u2010conformational subdomains of the Dsg3 ectodomain including recently described NH<jats:sub>2<\/jats:sub>\u2010terminal immunodominant epitopes. By ELISA, IgG reactivity against distinct subdomains of Dsg3 was related to disease activity and the clinical phenotype of PV patients. Our findings suggest that (i) autoantibody from PV sera react with non\u2010conformational epitopes of Dsg3; (ii) IgG reactivity against the NH<jats:sub>2<\/jats:sub>\u2010terminus and the extracellular domains (EC) 2\u20104 of Dsg3 was associated with active PV, while IgG titres were not strictly correlated with disease activity and (iii) IgG reactivity against the EC1\u20104 was associated with mucosal dominant PV and was decreased in cutaneous dominant PV. The findings may help to define more refined serological disease markers of PV.<\/jats:p>","DOI":"10.1111\/j.1600-0625.2007.00615.x","type":"journal-article","created":{"date-parts":[[2007,10,5]],"date-time":"2007-10-05T09:16:21Z","timestamp":1191575781000},"page":"35-43","source":"Crossref","is-referenced-by-count":41,"title":["IgG against extracellular subdomains of desmoglein 3 relates to clinical phenotype of pemphigus 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