A possible interaction between periostin and CD163+ skin‐resident macrophages in pemphigus vulgaris and bullous pemphigoid. Issue 12 (9th January 2017)

• Record Type: Journal Article
• Authors: Fujimura, Taku; Kakizaki, Aya; Furudate, Sadanori; Aiba, Setsuya
• Other Names: Antonicelli Frank guestEditor.; Ludwig Ralf J. guestEditor.
• Is Part Of: Experimental dermatology. Volume 26:Issue 12(2017)
• Page Start: 1193
• Page End: 1198
• Publication Date: 2017-01-09
• Subjects: CXCL5 -- IL‐36 -- pemphigus -- periostin -- tissue‐associated macrophages; Dermatology -- Periodicals; 616.5
• DOI: 10.1111/exd.13157
• Languages: English
• ISSNs: 0906-6705

Abstract

Abstract: Pemphigus vulgaris (PV) and bullous pemphigoid (BP) are autoimmune blistering diseases, and substantial numbers of CD163 + tissue‐associated macrophages (TAMs) are detected in both diseases. PV and BP possess different subsets of helper T cells, suggesting that the cytokine profiles of PV and BP might be different. The purpose of this study was to investigate the microenvironment of lesional skin and serum of PV and BP patients, focusing on the immunomodulatory factors related to TAMs, such as periostin (POSTN), chemokines, cytokines and matrix metalloproteinases (MMPs). We first performed immunohistological staining of POSTN in PV and BP lesions. POSTN was prominent in the superficial dermis in both PV and BP lesions. Next, to validate the activation of CD163 + TAMs in PV and BP patients, we examined the serum levels of soluble (s)CD163. The serum sCD163 levels in PV and BP patients are significantly higher than in healthy controls. To further elucidate the molecular mechanisms of the effects of POSTN on CD163 + TAMs in PV and BP, we examined chemokines, MMPs and cytokines selected by DNA microarray database. The serum CXCL5 levels from PV patients are significantly higher than those in BP patients and healthy controls. The IL‐36γ expression on infiltrating macrophages was prominent only in the lesional skin of PV, while the MMP12 deposition was detected in both PV and BP lesions. Our results shed light on the novel pathogenesis of PV through CD163 + TAMs.