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

被引:8
作者
Xu, Jun [1 ,4 ,5 ]
Lee, Jin-Woo [1 ]
Park, Soo-Kyoung [1 ]
Lee, Sung-Bok [2 ]
Yoon, Young-Hoon [1 ]
Yeon, Sun-Hee [1 ]
Rha, Ki-Sang [1 ]
Choi, Ji-Ae [3 ]
Song, Chang-Hwa [3 ]
Kim, Yong Min [1 ]
机构
[1] Chungnam Natl Univ, Sch Med, Dept Otorhinolaryngol Head & Neck Surg, Res Inst Med Sci, Daejeon, South Korea
[2] Chungnam Natl Univ, Sch Med, Chungnam Natl Univ Hosp, Dept Ophthalmol, Daejeon, South Korea
[3] Chungnam Natl Univ, Coll Med, Dept Microbiol, Daejeon, South Korea
[4] Guangzhou Med Univ, Affiliated Hosp 1, Dept Otorhinolaryngol Head & Neck Surg, State Key Lab Resp Dis, Guangzhou, Guangdong, Peoples R China
[5] Yanbian Univ Hosp, Dept Otorhinolaryngol Head & Neck Surg, Yanji, Jilin, Peoples R China
基金
新加坡国家研究基金会;
关键词
B-cell activating factor; Sinusitis; Nasal polyp; Toll-like receptor; Type I interferon; PLASMACYTOID DENDRITIC CELLS; ALPHA-PRODUCING CELLS; IMMUNE-COMPLEXES; BACTERIAL-DNA; SELF-DNA; C-CLASS; CPG; AUTOIMMUNITY; INFECTION; RESPONSES;
D O I
10.1016/j.clim.2018.07.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:19 / 26
页数:8
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