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Interleukin-36α axis is modulated in patients with primary Sjögren's syndrome.

Authors :
Ciccia, F.
Accardo‐Palumbo, A.
Alessandro, R.
Alessandri, C.
Priori, R.
Guggino, G.
Raimondo, S.
Carubbi, F.
Valesini, G.
Giacomelli, R.
Rizzo, A.
Triolo, G.
Source :
Clinical & Experimental Immunology. Aug2015, Vol. 181 Issue 2, p230-238. 9p. 1 Chart, 5 Graphs.
Publication Year :
2015

Abstract

The aim of this study was to investigate the expression of the interleukin (IL)-36 axis in patients with primary Sjögren's syndrome (pSS). Blood and minor labial salivary glands (MSG) biopsies were obtained from 35 pSS and 20 non-Sjögren's syndrome patients (nSS) patients. Serum IL-36α was assayed by enzyme-linked immunosorbent assay (ELISA). IL-36α, IL-36R, IL-36RA, IL-38, IL-22, IL-17, IL-23p19 and expression in MSGs was assessed by reverse transcription-polymerase chain reaction (RT-PCR), and tissue IL-36α and IL-38 expression was also investigated by immunohistochemistry (IHC). αβ and γδ T cells and CD68+ cells isolated from MSGs were also studied by flow cytometry and confocal microscopy analysis. IL-36α was over-expressed significantly in the serum and in the salivary glands of pSS. Salivary gland IL-36α expression was correlated with the expression levels of IL-17, IL-22 and IL-23p19. IL-38, that acts as inhibitor of IL-36α, was also up-regulated in pSS. αβ+ CD3+ T cells and CD68+ cells were the major source of IL-36α in minor salivary glands of pSS. γδ T cells were not significantly expanded in the salivary glands of pSS but produced more IL-17, as their percentage correlated with the focus score. Higher expression of IL-36α and IL-36R was also demonstrated in γδ T cells isolated from pSS compared to controls. In this study we demonstrate that a significant increase in circulating and tissue levels of IL-36α occurs in pSS patients. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00099104
Volume :
181
Issue :
2
Database :
Academic Search Index
Journal :
Clinical & Experimental Immunology
Publication Type :
Academic Journal
Accession number :
108353107
Full Text :
https://doi.org/10.1111/cei.12644