Decreased IL-10 production mediated by Toll-like receptor 9 in B cells in multiple sclerosis

被引:59
作者
Hirotani, Makoto
Niino, Masaaki [1 ]
Fukazawa, Toshiyuki [2 ]
Kikuchi, Seiji [3 ]
Yabe, Ichiro
Hamada, Shinsuke [4 ]
Tajima, Yasutaka [5 ]
Sasaki, Hidenao
机构
[1] Hokkaido Univ, Grad Sch Med, Dept Neurol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
[2] Sapporo Neurol Clin, Sapporo, Hokkaido, Japan
[3] Sapporo Minami Natl Hosp, Dept Neurol, Sapporo, Hokkaido, Japan
[4] Hokuyukai Neurol Hosp, Sapporo, Hokkaido, Japan
[5] Sapporo City Gen Hosp, Dept Neurol, Sapporo, Hokkaido, Japan
关键词
MS; TLR9; CpG DNA; Immunoregulation; DENDRITIC CELLS; T-CELLS; AUTOIMMUNE; MEMORY; TLR9;
D O I
10.1016/j.jneuroim.2010.02.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The complexity of the roles of Toll-like receptors (TLRs) is attributable to their ability to promote or suppress autoimmune diseases. Recent studies have demonstrated that B cells regulate autoimmune diseases, including multiple sclerosis (MS), by producing interleukin (IL)-10. By using CpG DNA as a TLR9 agonist, we investigated the immunoregulatory functions of B cell via TLR9 in MS. Our results indicate that TLR9-mediated IL-10 production by B cells was significantly decreased in MS, and this decrease is likely due to decreased TLR9 expression in memory B cells, suggesting a role of TLR9 in immunoregulation in MS. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:95 / 100
页数:6
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