| Literature DB >> 29222824 |
Rahel Thomi1, Christoph Schlapbach1, Nikhil Yawalkar1, Dagmar Simon1, Daniel Yerly2, Robert E Hunger1.
Abstract
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 CD4+ 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.Entities:
Keywords: T-cell proliferation; antimicrobial peptide; cytokine correlations; inflammatory skin disease; suggested pro-inflammatory loop
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Year: 2018 PMID: 29222824 DOI: 10.1111/exd.13482
Source DB: PubMed Journal: Exp Dermatol ISSN: 0906-6705 Impact factor: 3.960