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Elevated levels of the antimicrobial peptide LL ‐37 in hidradenitis suppurativa are associated with a Th1/Th17 immune response
Author(s) -
Thomi Rahel,
Schlapbach Christoph,
Yawalkar Nikhil,
Simon Dagmar,
Yerly Daniel,
Hunger Robert E.
Publication year - 2018
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/exd.13482
Subject(s) - cathelicidin , hidradenitis suppurativa , antimicrobial peptides , psoriasis , immune system , antimicrobial , peptide , downregulation and upregulation , immunology , medicine , chemokine , microbiology and biotechnology , biology , disease , gene , biochemistry
Hidradenitis suppurativa ( HS ) is an inflammatory skin disease with poorly understood immunopathogenic mechanisms. LL ‐37 is an antimicrobial peptide, which is transcribed from the CAMP (cathelicidin antimicrobial peptide) gene. Previous reports showed upregulated levels of CAMP and LL ‐37 in HS lesions, and therefore, the aim of this study was to compare levels of LL ‐37 in HS to other inflammatory skin diseases and to establish immunomodulatory functions of LL ‐37 in HS . We confirm an upregulation of the LL ‐37 peptide in lesional HS skin with comparable levels as in psoriasis patients and are able to positively correlate the presence of LL ‐37 in HS with the presence of T cells, macrophages, neutrophils, IFN ‐γ, IL ‐17, IL ‐23, TNF ‐α, IL ‐32 and IL ‐1β. Mechanistically, LL ‐37 boosts the proliferation of unspecifically activated CD 4 + T cells via an increased calcium signalling independent of antigen‐presenting cells. Targeting LL ‐37 may therefore represent a new therapeutic option for the treatment of this recalcitrant disease, but it has to be kept in mind that LL ‐37 also has an antimicrobial function.