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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,长的非编码RNA Neat1和Rig-I表达与活跃相中的HBeAg阳性慢性乙型肝炎患者有关

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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-naive 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:背景技术先天免疫在宿主病毒相互作用中起着至关重要的作用,并且大大影响了包括HBV感染的病毒复制。然而,很少有研究研究了TLRS,RIG-I和长编码RNA Neat1在临床样本中慢性HBV感染(CHB)患者的可能抗病毒免疫角色及其在免疫反应中的关系中。在这项研究中,我们试图研究HBEAG阳性CHB治疗 - 天真患者的TLR1-10,RIG-I和Neat1表达的mRNA表达水平。方法通过QPCR测量CHB患者CHB患者的TLR1-10,RIG-I和NEAT1的表达水平。还测量了包括ALT等在内的血清HBV DNA和常规肝脏生物化学,以评估受CHB影响的肝脏的生理功能受损。结果CHB中的TLR1和TLR6的表达水平显着低于健康对照的显着低。活性相的CHB患者的TLR3水平显着高于健康对照的患者。与健康对照相比,CHB患者的整个Neat1表达异常降低。与健康对照相比,CHB患者在CHB患者中,钻井平台的水平显着降低。 TLR6和Rig-i的表达与Neat1表达密切相关。 TLR6级别与钻机I级正相关。结论慢性HBV感染通过下调TLR1,TLR6,Neat1的功能表达可以改变先天免疫应答。

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