首页> 外文期刊>Journal of clinical laboratory analysis. >Toll‐like receptors, long non‐coding RNA NEAT1, and RIG‐I expression are associated with HBeAg‐positive chronic hepatitis B patients in the active phase
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Toll‐like receptors, long non‐coding RNA NEAT1, and RIG‐I expression are associated with HBeAg‐positive chronic hepatitis B patients in the active phase

机译:Toll样受体,长非编码RNA NEAT1和RIG-I表达与HBeAg阳性慢性乙型肝炎患者处于活动期有关

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Background Innate immunity plays a crucial role in host‐virus interactions and greatly influences viral replication including HBV infection. However, few studies have investigated the possible antiviral immune roles played by TLRs, RIG‐I, and long no‐coding RNA NEAT1 in chronic HBV infection (CHB) patients in clinical samples and their relationships among immune responses. In this study, we sought to investigate the mRNA expression levels of TLR1‐10, RIG‐I, and NEAT1 expression in HBeAg‐positive CHB treatment‐na?ve patients with the active phase. Methods The expression levels of TLR1‐10, RIG‐I, and NEAT1 of CHB patients with the active phase and healthy controls were measured by qPCR. Serum HBV DNA and routine liver biochemistry including ALT, etc were also measured to evaluate the impaired physiological function of the liver affected by CHB. Results The expression levels of TLR1 and TLR6 in CHB with active phase were remarkably lower than that in healthy controls. The levels of TLR3 in CHB patients with active phase were remarkably higher than that in healthy controls. The total NEAT1 expression was abnormally decreased in CHB patients as compared with healthy controls. The levels of RIG‐I were significantly decreased in CHB patients in the active phase when compared to healthy controls. The expression of TLR6 and RIG‐I was closely correlated with NEAT1 expression. TLR6 level was positively correlated with RIG‐I level. Conclusion Chronic HBV infection can alter the innate immune response by downregulating functional expression of TLR1, TLR6, NEAT1.
机译:背景先天免疫在宿主病毒相互作用中起着至关重要的作用,并极大地影响包括HBV感染在内的病毒复制。但是,很少有研究调查在临床样本的慢性HBV感染(CHB)患者中TLR,RIG-I和长无编码RNA NEAT1可能发挥的抗病毒免疫作用及其在免疫应答之间的关系。在这项研究中,我们试图调查HBeAg阳性CHB治疗初治活动期患者中TLR1-10,RIG-1和NEAT1 mRNA的表达水平。方法采用qPCR检测活跃期CHB患者和健康对照者TLR1-10,RIG-1和NEAT1的表达水平。还测量了血清HBV DNA和常规的肝脏生物化学(包括ALT等),以评估受CHB影响的肝脏的生理功能受损。结果活动期CHB中TLR1和TLR6的表达水平明显低于健康对照组。活动期CHB患者的TLR3水平明显高于健康对照组。与健康对照组相比,CHB患者的总NEAT1表达异常降低。与健康对照组相比,活跃期CHB患者的RIG-I水平显着降低。 TLR6和RIG-I的表达与NEAT1的表达密切相关。 TLR6水平与RIG-I水平呈正相关。结论慢性HBV感染可通过下调TLR1,TLR6,NEAT1的功能性表达来改变先天免疫应答。

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