Toll-like receptor 9 ligands increase type I interferon induced B-cell activating factor expression in chronic rhinosinusitis with nasal polyposis

Copyright © 2018 Elsevier Inc. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 197(2018) vom: 01. Dez., Seite 19-26
1. Verfasser: Xu, Jun (VerfasserIn)
Weitere Verfasser: Lee, Jin-Woo, Park, Soo-Kyoung, Lee, Sung-Bok, Yoon, Young-Hoon, Yeon, Sun-Hee, Rha, Ki-Sang, Choi, Ji-Ae, Song, Chang-Hwa, Kim, Yong Min
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2018
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Research Support, Non-U.S. Gov't B-cell activating factor Nasal polyp Sinusitis Toll-like receptor Type I interferon B-Cell Activating Factor HMGB1 Protein HMGB1 protein, human mehr... Interferon-alpha RNA, Messenger TLR9 protein, human TNFSF13B protein, human Toll-Like Receptor 9 Interferon-beta 77238-31-4
Beschreibung
Zusammenfassung:Copyright © 2018 Elsevier Inc. All rights reserved.
B-cell activating factor (BAFF) has been proposed to play a crucial role in the pathogenesis of chronic rhinosinusitis with nasal polyp (CRSwNP). The aim of this study was to evaluate the role of toll-like receptor (TLR) 9-mediated BAFF activation on the pathogenesis of CRSwNP. NP and uncinate tissue (UT) were obtained from patients with CRSwNP or CRS without NP, and control subjects. The expression of TLR9, high mobility group box-1 protein (HMGB1), type I interferon (IFN), BAFF, and anti-double stranded DNA (dsDNA) antibody were examined in the tissues and the cultured dispersed NP cells (DNPCs). The expression of TLR9, HMGB1, type I IFN, BAFF, and anti-dsDNA antibody were elevated in NP tissue compared to the UTs. Exposure to TLR9 agonist increased the type I IFN expression in vitro, which further increased BAFF production. In conclusion, we provided a novel therapeutic potential of TLR9 agonist in CRSwNP
Beschreibung:Date Completed 07.10.2019
Date Revised 07.10.2019
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2018.07.014