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MS2 VLP-based delivery of microRNA-146a inhibits autoantibody production in lupus-prone mice

机译:基于MS2 VLP的microRNA-146a传递抑制易患狼疮的小鼠自身抗体的产生

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摘要

BackgroundSystemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by the presence of pathogenic autoantibodies. Recent studies suggest that microRNAs (miRNAs) play an essential role in immunoregulation and may be involved in the pathogenesis of SLE. Therefore, it was of interest to investigate the potential therapeutic application of miRNAs in SLE, a concept that has not been thoroughly investigated thus far. Virus-like particles (VLPs) are a type of recombinant nanoparticle enveloped by certain proteins derived from the outer coat of a virus. Herein, we describe a novel miRNA-delivery approach via bacteriophage MS2 VLPs and investigate the therapeutic effects of miR-146a, a well-studied and SLE-related miRNA, in BXSB lupus-prone mice.
机译:背景系统性红斑狼疮(SLE)是一种慢性自身免疫性疾病,其特征是存在致病性自身抗体。最近的研究表明,microRNA(miRNA)在免疫调节中起重要作用,并可能参与SLE的发病机理。因此,研究miRNA在SLE中的潜在治疗应用非常有趣,这一概念至今尚未得到彻底研究。病毒样颗粒(VLP)是一种重组纳米颗粒,被源自病毒外壳的某些蛋白质包裹。在这里,我们描述了一种通过噬菌体MS2 VLP传递miRNA的新方法,并研究了易患BXSB狼疮小鼠miR-146a(一种经过充分研究且与SLE相关的miRNA)的治疗作用。

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