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Detection of perforin and granzyme B mRNA expressing cells in lichen sclerosus
Author(s) -
Hunger Robert E.,
Brönnimann Marcel,
Kappeler Andreas,
Mueller Christoph,
Braathen Lasse R.,
Yawalkar Nikhil
Publication year - 2007
Publication title -
experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.108
H-Index - 96
eISSN - 1600-0625
pISSN - 0906-6705
DOI - 10.1111/j.1600-0625.2007.00543.x
Subject(s) - granzyme b , perforin , granzyme , granzyme a , cytotoxic t cell , biology , cd8 , in situ hybridization , immunohistochemistry , pathology , immunology , microbiology and biotechnology , messenger rna , immune system , medicine , in vitro , gene , biochemistry
Granzyme B and perforin messenger RNA (mRNA) expression has been shown to be a specific in vivo activation marker for cytotoxic cells. The aim of this study was to assess the contribution of cell‐mediated cytotoxicity in the pathogenesis of lichen sclerosus. In situ hybridization and immunohistochemistry were performed on serial tissue sections of lesional skin biopsies and normal skin as control. Immunohistochemical staining showed that the cellular infiltrate of diseased skin consisted predominantly of T cells (CD3+) and some B cells (CD20+). Among T cells CD4+ and CD8+ cells were found in about equal numbers. In normal skin samples perforin and granzyme B mRNA expressing cells were only rarely found. In contrast, in biopsies from diseased skin a high percentage of infiltrating cells expressed mRNA for perforin and granzyme B. The perforin and granzyme B expressing cells were found in the dermal infiltrate and intraepidermally in close proximity to keratinocytes suggesting in situ activation of these cells. These findings provide evidence that cell‐mediated cytotoxicity plays a significant role in tissue destruction in lichen sclerosus.