Toll-like receptors pathway in common variable immune deficiency (CVID) and X-linked agammaglobulinemia (XLA).

IF 2.2 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Parsova Tavasolian, Laleh Sharifi, Asghar Aghamohammadi, Farshid Noorbakhsh, Rouzbeh Sanaei, Mahsima Shabani, Nima Rezaei
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引用次数: 2

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.

共同可变免疫缺陷(CVID)和x连锁无球蛋白血症(XLA)中的toll样受体途径。
常见可变免疫缺陷(CVID)和x连锁无球蛋白血症(XLA)是两种主要的体液免疫缺陷,导致儿童早期死亡率很高。为了确定CVID和XLA的发病机制可能涉及的因素,近年来的研究主要集中在toll样受体(Toll-like receptor, TLRs)上,并揭示了CVID和XLA患者免疫细胞中不同TLR通路的缺陷。本研究中,我们测量了CVID和XLA患者外周血单个核细胞(PBMCs)中TLR-4和TLR-9 RNA水平,从而测量了TNF-α和IFN-α的产生。与健康个体相反,配体刺激后,TLR-9的表达没有显著增加,而配体诱导的TLR-4的表达与健康对照无显著差异。与对照组相比,脂多糖(LPS)刺激的TNF-α产生在患者中显著减少,而在CpG刺激后,所有组的IFN-α产生均增加,组间无显著差异。我们的数据表明,TLR-9激活通路的缺陷可能是TLR-9表达减少的结果,尽管TLR-9不是这些患者中IFN-α产生的唯一调节剂。另一方面,TLR-4激活通路中的信号通路受损导致TNF-α产生显著减少,这与TLR-4表达缺陷无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European cytokine network
European cytokine network 生物-免疫学
CiteScore
5.70
自引率
0.00%
发文量
5
审稿时长
6 months
期刊介绍: The journal that brings together all areas of work involving cytokines. European Cytokine Network is an electronic journal that publishes original articles and abstracts every quarter to provide an essential bridge between researchers and clinicians with an interest in this cutting-edge field. The journal has become a must-read for specialists in the field thanks to its swift publication and international circulation. The journal is referenced in several databases, including Medline, which is testament to its scientific quality.
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