Tavasolian Parsova, Sharifi Laleh, Aghamohammadi Asghar, Noorbakhsh Farshid, Sanaei Rouzbeh, Shabani Mahsima, Rezaei Nima
Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Eur Cytokine Netw. 2018 Nov 1;29(4):153-158. doi: 10.1684/ecn.2018.0420.
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.
常见变异型免疫缺陷(CVID)和X连锁无丙种球蛋白血症(XLA)是两种主要的体液免疫缺陷疾病,可导致儿童早期死亡率很高。为了确定可能参与CVID和XLA发病机制的因素,最近的研究集中在Toll样受体(TLR)上,并证明了CVID和XLA患者免疫细胞中不同TLR途径存在缺陷。在此,我们检测了CVID和XLA患者外周血单个核细胞(PBMC)中TLR-4和TLR-9的RNA水平,以及随后肿瘤坏死因子-α(TNF-α)和干扰素-α(IFN-α)的产生情况。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表达与健康对照PBMC中的表达没有显著差异。与对照组相比,患者中脂多糖(LPS)刺激的TNF-α产生显著减少,而在所有组中,经CpG刺激后IFN-α的产生均增加,组间无显著差异。我们的数据表明,TLR-9激活途径的缺陷可能是TLR-9表达降低的结果,尽管TLR-9不是这些患者中IFN-α产生的唯一调节因子。另一方面,TLR-4激活途径中信号传导受损导致TNF-α产生显著减少,这与TLR-4表达缺陷无关。