Toll-like receptor 2 is highly expressed in lesions of acne inversa and colocalizes with C-type lectin receptor

Hunger, R E; Surovy, A M; Hassan, A S; Braathen, L R; Yawalkar, N (2008). Toll-like receptor 2 is highly expressed in lesions of acne inversa and colocalizes with C-type lectin receptor. British journal of dermatology, 158(4), pp. 691-7. Oxford: Wiley-Blackwell 10.1111/j.1365-2133.2007.08425.x

Full text not available from this repository. (Request a copy)

BACKGROUND: Acne inversa (hidradenitis suppurativa) is a chronic inflammatory and cicatricial disorder that affects skin areas rich in apocrine glands and terminal hairs, such as perineum and axillae. The exact pathogenesis of the disease is not well understood and the mechanisms by which bacterial superinfection contributes to the disease progression are not clear. Toll-like receptors (TLRs) expressed by inflammatory cells play a crucial role in the innate immune response to bacteria. OBJECTIVES: We sought to investigate the role of TLR2 in the pathogenesis of acne inversa. METHODS: We investigated the expression of TLR2 using real-time polymerase chain reaction analysis and immunohistochemical stainings of tissue samples from patients with acne inversa. Furthermore, we phenotypically characterized the infiltrating cells and their expression of TLR2. RESULTS: Compared with normal skin, a highly increased in situ expression of TLR2 in acne inversa skin lesions was found at both the mRNA and the protein level. The most abundant cells in the dermal infiltrate of acne inversa were CD68+ macrophages, CD209+ dendritic cells (DCs) and CD3+ T cells. CD19+ B cells and CD56+ natural killer cells were found only in small numbers. Double staining with fluorescence-labelled antibodies showed that TLR2 was expressed by infiltrating macrophages (CD68+) and DCs (CD209+). Flow cytometric analysis of isolated infiltrating cells further confirmed surface expression of TLR2 by macrophages and DCs. CONCLUSIONS: These data indicate that the enhanced expression of TLR2 by infiltrating macrophages and DCs may contribute to the pathogenesis of inflammatory lesions of acne inversa.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Department of Dermatology, Urology, Rheumatology, Nephrology, Osteoporosis (DURN) > Clinic of Dermatology

UniBE Contributor:

Hunger, Robert; Surovy, André Martin and Yawalkar, Nikhil

ISSN:

0007-0963

ISBN:

18241264

Publisher:

Wiley-Blackwell

Language:

English

Submitter:

Factscience Import

Date Deposited:

04 Oct 2013 15:04

Last Modified:

04 May 2014 23:19

Publisher DOI:

10.1111/j.1365-2133.2007.08425.x

PubMed ID:

18241264

Web of Science ID:

000254122100004

URI:

https://boris.unibe.ch/id/eprint/27676 (FactScience: 109906)

Actions (login required)

Edit item Edit item
Provide Feedback