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Sequence-dependent Stimulation of the Mammalian Innate Immune Response by Synthetic Sirna

Nature Biotechnology(2005)

Protiva Biotherapeutics

Cited 1161|Views27
Abstract
Short interfering RNAs (siRNAs) that mediate specific gene silencing through RNA interference (RNAi) are widely used to study gene function and are also being developed for therapeutic applications 1 . Many nucleic acids, including double- (dsRNA) 2 and single-stranded RNA (ssRNA) 3 , 4 , 5 , can stimulate innate cytokine responses in mammals. Despite this, few studies have questioned whether siRNA may have a similar effect on the immune system 6 , 7 . This could significantly influence the in vivo application of siRNA owing to off-target effects and toxicities associated with immune stimulation. Here we report that synthetic siRNAs formulated in nonviral delivery vehicles can be potent inducers of interferons and inflammatory cytokines both in vivo in mice and in vitro in human blood. The immunostimulatory activity of formulated siRNAs and the associated toxicities are dependent on the nucleotide sequence. We have identified putative immunostimulatory motifs that have allowed the design of siRNAs that can mediate RNAi but induce minimal immune activation.
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Life Sciences,general,Biotechnology,Biomedicine,Agriculture,Biomedical Engineering/Biotechnology,Bioinformatics
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要点】:该论文发现合成小干扰RNA(siRNA)在非病毒载体中可以强烈刺激哺乳动物的固有免疫反应,其免疫刺激活性及相关的毒性取决于核苷酸序列,研究确定了可能的免疫刺激性基序,从而设计了既能实现RNA干扰又能最小化免疫激活的siRNA。

方法】:研究者使用了非病毒载体来传递合成siRNA,并在小鼠体内及人类血液中体外评估了这些siRNA对干扰素和炎症细胞因子的诱导作用。

实验】:实验结果显示, formulated siRNAs具有免疫刺激活性,相关的毒性也受到核苷酸序列的影响。通过识别免疫刺激性基序,研究者能够设计出既能够执行RNA干扰功能,又能最小化免疫激活的siRNA。具体数据集中文名称未提供,但实验结果表明这些设计 siRNA在体内外均表现出较低的免疫原性。