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Liver fibrosis is associated with cutaneous inflammation in the imiquimod‐induced murine model of psoriasiform dermatitis
Author(s) -
Vasseur P.,
Pohin M.,
Jégou J.F.,
Favot L.,
Venisse N.,
Mcheik J.,
Morel F.,
Lecron J.C.,
Silvain C.
Publication year - 2018
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/bjd.16137
Subject(s) - psoriasis , medicine , inflammation , fibrosis , hepatitis , pathology , dermatology , immunology
Summary Background Psoriasis exhibits several extracutaneous manifestations. Little is known about hepatic parameters specifically associated with psoriasis. Objectives To study whether psoriasiform dermatitis is associated with liver injury. Methods We studied liver parameters of inflammation and fibrosis in a murine model of psoriasiform dermatitis induced by topical application of imiquimod for 9 weeks. Results Topical treatment with imiquimod induced a form of psoriasiform dermatitis reminiscent of the human disorder, characterized by thickened and scaly skin, psoriasiform epidermal hyperplasia, altered keratinocyte differentiation and cutaneous overexpression of interleukin‐17A. Mice with dermatitis displayed hepatitis, as shown by elevation of plasma transaminase levels, as well as portal and periportal hepatitis, characterized by T‐lymphocyte ( CD 3ε + ) and polymorphonuclear cell (Gr1 + ) infiltrates. The hepatitis progressed towards liver fibrogenesis, as shown by excessive Sirius red staining, which is consistent with the expression of α‐smooth muscle actin by hepatic stellate cells. Conclusions These results indicate that liver inflammation and fibrosis are associated with experimental psoriasiform dermatitis. Our results suggest that psoriatic inflammation may be associated with specific liver injury.