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Efficacy of cationic lipid-DNA complexes (CLDC) on hepatitis B virus in transgenic mice.

机译:阳离子脂质-DNA复合物(CLDC)对转基因小鼠乙型肝炎病毒的功效。

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摘要

Cationic lipid-DNA (non-coding) complexes (CLDC) are activators of the innate immune response that increase survival of rodents with some acute viral infections and cancers. CLDC were evaluated for their ability to impact viral DNA levels in transgenic mice carrying an infectious clone of hepatitis B virus (HBV). Mice used in the studies were diet-restricted as nursing pups from solid food, because the expression of HBV DNA in the liver was increased above background levels in some mice with this restriction. Survival surgery was performed on these mice to obtain liver biopsies from which to select animals with suitable levels of liver HBV DNA for entry into the experimental protocols. Intravenous administration of 5mug/mouse of CLDC on days 1, 7 and 13 reduced liver HBV DNA to similar low levels achieved with the positive control, adefovir dipivoxil. In a subsequent experiment, the same treatment schedule was used to determine that the minimal effective CLDC dose was between 0.5 and 0.05mug/mouse. Selective cytokines were increased in the livers of CLDC-treated compared to placebo-treated mice in a dose-responsive manner. CLDC were effective in reducing liver HBV DNA and could be considered for further evaluation in other hepatitis models.
机译:阳离子脂质DNA(非编码)复合物(CLDC)是先天免疫应答的激活剂,可增加啮齿动物在某些急性病毒感染和癌症中的存活率。在携带乙型肝炎病毒(HBV)传染性克隆的转基因小鼠中,评估了CLDC对病毒DNA水平的影响能力。该研究中使用的小鼠在饮食上被限制为固体食物中的哺乳幼崽,因为在某些受到这种限制的小鼠中,肝脏中HBV DNA的表达增加到高于背景水平。对这些小鼠进行了生存手术,以获取肝脏活检样本,从中选择具有适当水平的肝HBV DNA的动物以进入实验方案。在第1、7和13天静脉给予5杯/小鼠CLDC,可将肝脏HBV DNA降低至与阳性对照阿德福韦酯(Devivoxil)相似的低水平。在随后的实验中,使用相同的治疗方案来确定最小有效CLDC剂量在0.5至0.05杯/小鼠之间。与安慰剂治疗的小鼠相比,CLDC治疗的肝脏中的选择性细胞因子以剂量反应方式增加。 CLDC可有效减少肝脏HBV DNA,并可以考虑在其他肝炎模型中进行进一步评估。

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