{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,27]],"date-time":"2026-09-27T23:51:33Z","timestamp":1790553093083,"version":"4.1.0"},"reference-count":52,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2016,10,21]],"date-time":"2016-10-21T00:00:00Z","timestamp":1477008000000},"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":[[2017,5]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      Cutaneous (\n                      <jats:styled-content style=\"fixed-case\">CLP<\/jats:styled-content>\n                      ) and oral lichen planus (\n                      <jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>\n                      ) as the main subtypes of lichen planus (\n                      <jats:styled-content style=\"fixed-case\">LP<\/jats:styled-content>\n                      ) present with different clinical manifestation and disease course, although their histopathologic features such as the band\u2010like lymphocyte infiltrate and keratinocyte apoptosis are similar. So far, the underlying cellular and molecular mechanisms remain poorly understood.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>\n                      The aim of this study was to characterize and compare the\n                      <jats:italic>in situ<\/jats:italic>\n                      cellular infiltrates, cytokine expression profiles and apoptosis markers in\n                      <jats:styled-content style=\"fixed-case\">CLP<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Using immunofluorescence staining and laser scanning microscopy, we evaluated the cellular infiltrate (\n                      <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                      1a,\n                      <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                      3,\n                      <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                      4,\n                      <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                      8,\n                      <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                      21,\n                      <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                      57,\n                      <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                      123), cytokine expression (interleukin (\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      )\u20101,\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u20106,\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u20109,\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u201010,\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u201017,\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u201022,\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u201023, tumour necrosis factor\u2010\u03b1, transforming growth factor\u2010\u03b2, interferon (\n                      <jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\n                      )\u2010\u03b3), and apoptosis markers (Fas, Fas ligand, cleaved caspase\u20103,\n                      <jats:styled-content style=\"fixed-case\">TUNEL<\/jats:styled-content>\n                      ) of 21 anonymized biopsy specimens of\n                      <jats:styled-content style=\"fixed-case\">LP<\/jats:styled-content>\n                      (11\n                      <jats:styled-content style=\"fixed-case\">CLP<\/jats:styled-content>\n                      , 10\n                      <jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>\n                      ).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Among infiltrating cells mainly T cells and natural killer (\n                      <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content>\n                      ) cells as well as plasmacytoid dendritic cells (\n                      <jats:styled-content style=\"fixed-case\">DC<\/jats:styled-content>\n                      ) were observed. A predominance of\n                      <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                      8+ T cells was noted in\n                      <jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>\n                      . In both\n                      <jats:styled-content style=\"fixed-case\">CLP<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>\n                      , T helper (Th)1, Th9, Th17, and Th22\u2010type cytokines were expressed. The expression of\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u20109,\n                      <jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\n                      \u2010\u03b3 and\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u201022 was higher in\n                      <jats:styled-content style=\"fixed-case\">CLP<\/jats:styled-content>\n                      compared to that of\n                      <jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>\n                      (\n                      <jats:italic>P<\/jats:italic>\n                      = 0.0165;\n                      <jats:italic>P<\/jats:italic>\n                      = 0.0016;\n                      <jats:italic>P<\/jats:italic>\n                      = 0.052 respectively). Expression of Fas and Fas ligand as well as cleaved caspase\u20103\u2010positive cells was observed in the epithelium of all\n                      <jats:styled-content style=\"fixed-case\">LP<\/jats:styled-content>\n                      samples.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      The cell and cytokine patterns of\n                      <jats:styled-content style=\"fixed-case\">CLP<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>\n                      were partially distinct and generally resembled those reported for autoimmune diseases. The presence of\n                      <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                      8+ and\n                      <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content>\n                      cells as well as Fas\/Fas ligand expression suggested that various pathways involved in keratinocyte apoptosis are relevant for\n                      <jats:styled-content style=\"fixed-case\">LP<\/jats:styled-content>\n                      . These results might help to establish targeted therapies for\n                      <jats:styled-content style=\"fixed-case\">LP<\/jats:styled-content>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/jdv.13989","type":"journal-article","created":{"date-parts":[[2016,10,7]],"date-time":"2016-10-07T08:36:39Z","timestamp":1475829399000},"page":"880-886","source":"Crossref","is-referenced-by-count":32,"title":["Distinct interferon\u2010gamma and interleukin\u20109 expression in cutaneous and oral lichen planus"],"prefix":"10.1111","volume":"31","author":[{"given":"B.","family":"Weber","sequence":"first","affiliation":[{"name":"Department of Dermatology Inselspital, Bern University Hospital University of Bern Bern Switzerland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C.","family":"Schlapbach","sequence":"additional","affiliation":[{"name":"Department of Dermatology Inselspital, Bern University Hospital 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