首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Toll-like receptors pathway in common variable immune deficiency (CVID) and X-linked agammaglobulinemia (XLA)
Authors:Parsova?Tavasolian  Laleh?Sharifi  Asghar?Aghamohammadi  Farshid?Noorbakhsh  Rouzbeh?Sanaei  Mahsima?Shabani  Email author" target="_blank">Nima?Rezaei
Institution:1.Department of Immunology, School of Medicine,Tehran University of Medical Sciences,Tehran,Iran;2.Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children’s Medical Center,Tehran University of Medical Sciences,Tehran,Iran;3.Primary Immunodeficiency Diseases Network (PIDNet),Universal Scientific Education and Research Network (USERN),Tehran,Iran;4.Department of Immunology, School of Medicine,Iran University of Medical Sciences,Tehran,Iran;5.International Hematology/Oncology of Pediatrics Experts (IHOPE),Universal Scientific Education and Research Network (USERN),Tehran,Iran;6.Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA),Universal Scientific Education and Research Network (USERN),Tehran,Iran;7.Children’s Medical Center Hospital,Tehran,Iran
Abstract:Common variable immunodeficiency (CVID) and X-linked agammaglobulinemia (XLA) are two major humoral immunodeficiencies, causing a high rate of early age mortality in children. In order to identifiy the possible factors involved in the pathogenesis of CVID and XLA, recent studies have focused on Toll-like receptors (TLRs) and demonstrate the defects in different TLR pathways in immune cells of CVID and XLA patients. Herein, we measured TLR-4 and TLR-9 RNA levels and consequently TNF-α and IFN-α production in peripheral blood mononuclear cells (PBMCs) of patients with CVID and XLA. Contrary to healthy individuals, TLR-9 expression was not significantly increased after ligand stimulation, whereas ligand-induced TLR-4 expression was not significantly different from that in healthy control PBMCs. Lipopolysaccharide (LPS)-stimulated TNF-α production was significantly reduced in patients compared to controls, whereas IFN-α production was increased in all groups after CpG stimulation without any significant inter-group difference. Our data suggest that defects in TLR-9 activated pathways may be a result of the decreased TLR-9 expression, although TLR-9 is not the only modulator of IFN-α production in these patients. On the other hand, impaired signaling in TLR-4 activated pathways which results in significant reduction in TNF-α production are not related to a defect in TLR-4 expression.
Keywords:
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号