首页> 外文期刊>Nucleic Acid Therapeutics >Absence of Unspecific Innate Immune Cell Activation by GATA-3-SpecificTI Absence of Unspecific Innate Immune Cell Activation by GATA-3-Specific DNAzymes
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Absence of Unspecific Innate Immune Cell Activation by GATA-3-SpecificTI Absence of Unspecific Innate Immune Cell Activation by GATA-3-Specific DNAzymes

机译:GATA-3-SpecificTI缺乏非特异性先天免疫细胞的激活GATA-3-SpecificTI缺乏非特异性先天免疫细胞的激活

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摘要

DNAzymes of the 10-23 family represent an important class of antisense molecules with implications for therapeutic treatment of diseases. These molecules are single-stranded oligodeoxynucleotides combining the high specificity of oligonucleotide base pairing with an inherent RNA-cleaving enzymatic activity. However, like other oligonucleotide-based molecules these substances might exert so-called off-target effects, which have not been investigated so far for this molecule class. Therefore, the present study investigates putative off-target effects of DNAzymes on innate immune mechanisms using GATA-3-specific DNAzymes that have recently been developed as novel therapeutic approach for the treatment of allergic diseases including allergic asthma. The conserved catalytic domain of 10-23 DNAzymes contains a CpG motif that may stimulate innate immune cells via Toll-like receptor 9 (TLR-9). Therefore, potential TLR-9-mediated as well as TLR-9 independent cell activation was investigated using TLR-9-transfected HEK293 cells, macrophage cell lines and primary innate immune cells. Furthermore, putative effects of GATA-3-specific DNAzymes on the activation of neutrophil granulocytes and degranulation of mast cells/basophils were analyzed. In summary, no innate immune cell-stimulating activities of the tested DNAzymes were observed in any of the systems. Consequently, use of GATA-3-specific DNAzymes may represent a novel and highly specific approach for the treatment of allergic diseases.
机译:10-23家族的DNA酶代表一类重要的反义分子,对疾病的治疗具有重要意义。这些分子是单链寡脱氧核苷酸,结合了寡核苷酸碱基配对的高特异性和固有的RNA裂解酶活性。但是,像其他基于寡核苷酸的分子一样,这些物质可能会产生所谓的脱靶效应,目前尚未对该分子类别进行研究。因此,本研究使用最近被开发为治疗包括过敏性哮喘在内的变应性疾病的新型治疗方法的GATA-3特异性DNA酶来研究DNA酶对先天免疫机制的假定脱靶作用。 10-23 DNA酶的保守催化结构域包含一个CpG基序,可以通过Toll样受体9(TLR-9)刺激先天免疫细胞。因此,使用TLR-9转染的HEK293细胞,巨噬细胞系和原发性先天免疫细胞研究了潜在的TLR-9介导的以及TLR-9独立的细胞活化。此外,分析了GATA-3特异性DNA酶对嗜中性粒细胞的活化和肥大细胞/嗜碱性粒细胞脱粒的推定作用。总之,在任何系统中都没有观察到被测DNA酶的先天免疫细胞刺激活性。因此,使用GATA-3特异性DNA酶可能代表了一种新颖且高度特异性的方法来治疗过敏性疾病。

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