{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T20:26:15Z","timestamp":1782937575543,"version":"3.54.5"},"reference-count":37,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2018,2,27]],"date-time":"2018-02-27T00:00:00Z","timestamp":1519689600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Acad Dermatol Venereol"],"published-print":{"date-parts":[[2018,6]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Polymorphic light eruption (<jats:styled-content style=\"fixed-case\">PLE<\/jats:styled-content>) is the most common autoimmune photodermatosis. Plasmacytoid dendritic cells (<jats:styled-content style=\"fixed-case\">PDC<\/jats:styled-content>s) are important mediators of innate antimicrobial immunity involved in the pathogenesis of many inflammatory skin diseases. In addition to <jats:styled-content style=\"fixed-case\">PDC<\/jats:styled-content>s, regulatory T cells (Tregs) are involved in controlling inflammation and adaptive immunity in skin by their immunosuppressive capacity.<\/jats:p><\/jats:sec><jats:sec><jats:title>Objective<\/jats:title><jats:p>The aim of this study was to investigate the presence of <jats:styled-content style=\"fixed-case\">PDC<\/jats:styled-content>s and Tregs in photoexposed skin from <jats:styled-content style=\"fixed-case\">PLE<\/jats:styled-content> compared to healthy skin.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Patients with <jats:styled-content style=\"fixed-case\">PLE<\/jats:styled-content> diagnosis and healthy controls were recruited and underwent a photoprovocative test. A 4\u2010mm punch biopsy was taken from the site of positive photoprovocation test reaction, and immunohistochemistry for <jats:styled-content style=\"fixed-case\">BDCA<\/jats:styled-content>2 as marker for <jats:styled-content style=\"fixed-case\">PDC<\/jats:styled-content>s, <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4 and <jats:styled-content style=\"fixed-case\">FOXP<\/jats:styled-content>3 as markers for Tregs was performed. Double immunostain for <jats:styled-content style=\"fixed-case\">FOXP<\/jats:styled-content>3 and <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4 was performed as well. Absolute counts for <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4, <jats:styled-content style=\"fixed-case\">BDCA<\/jats:styled-content>2 and <jats:styled-content style=\"fixed-case\">FOXP<\/jats:styled-content>3 were performed in at least 5 High Power Fields (<jats:styled-content style=\"fixed-case\">HPF<\/jats:styled-content>). Percentage of <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4\u2010, <jats:styled-content style=\"fixed-case\">BDCA<\/jats:styled-content>2\u2010 and <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:styled-content style=\"fixed-case\">FOXP<\/jats:styled-content>3\u2010positive cells over the total inflammatory infiltrate was assessed for each case.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>We enrolled 23 patients and controls. <jats:styled-content style=\"fixed-case\">BDCA<\/jats:styled-content>2+ cells were present in 91.3% of <jats:styled-content style=\"fixed-case\">PLE<\/jats:styled-content> skin samples and 100% of healthy volunteer. Both in <jats:styled-content style=\"fixed-case\">PLE<\/jats:styled-content> patients and healthy controls, <jats:styled-content style=\"fixed-case\">PDC<\/jats:styled-content>s distribution was mainly dermic (<jats:italic>P<\/jats:italic> &lt; 0.05). Compared to healthy controls, both epidermic and dermic <jats:styled-content style=\"fixed-case\">BDCA<\/jats:styled-content>2+ cells count were significantly higher in <jats:styled-content style=\"fixed-case\">PLE<\/jats:styled-content> patients (<jats:italic>P<\/jats:italic> &lt; 0.05). Both in <jats:styled-content style=\"fixed-case\">PLE<\/jats:styled-content> patients and healthy controls, Tregs distribution was mainly dermic (<jats:italic>P<\/jats:italic> &lt; 0.05). The presence of both <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4+ cells and <jats:styled-content style=\"fixed-case\">FOXP<\/jats:styled-content>3+ cells was significantly higher in the dermis of <jats:styled-content style=\"fixed-case\">PLE<\/jats:styled-content> patients compared to controls (<jats:italic>P<\/jats:italic> &lt; 0.05). Relative percentages of cellular infiltrations confirmed these results.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>D\u2010<jats:styled-content style=\"fixed-case\">PDCS<\/jats:styled-content> and Tregs may play a significant role in the development of <jats:styled-content style=\"fixed-case\">PLE<\/jats:styled-content>, and dermal distribution of <jats:styled-content style=\"fixed-case\">PDC<\/jats:styled-content>s in <jats:styled-content style=\"fixed-case\">PLE<\/jats:styled-content> skin biopsies seems to confirm a possible overlap with cutaneous lupus erythematosus (<jats:styled-content style=\"fixed-case\">CLE<\/jats:styled-content>).<\/jats:p><\/jats:sec>","DOI":"10.1111\/jdv.14866","type":"journal-article","created":{"date-parts":[[2018,2,11]],"date-time":"2018-02-11T14:32:34Z","timestamp":1518359554000},"page":"985-991","source":"Crossref","is-referenced-by-count":14,"title":["Cutaneous infiltration of plasmacytoid dendritic cells and T 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