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Inhibitory/Suppressive Oligodeoxynucleotide Nanocapsules as Simple Oral Delivery Devices for Preventing Atopic Dermatitis in Mice

机译:抑制性/抑制性寡聚脱氧核苷酸纳米胶囊作为预防小鼠特应性皮炎的简单口服给药装置。

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摘要

Here, we report a simple and low-cost oral oligodeoxynucleotide (ODN) delivery system targeted to the gut Peyer's patches (PPs). This system requires only Dulbecco's modified eagle's medium, calcium chloride, ODNs, and basic laboratory equipment. ODN nanocapsules (ODNcaps) were directly delivered to the PPs through oral administration and were taken up by macrophages in the PPs, where they induced an immune response. Long-term continuous oral dosing with inhibitory/suppressive ODNcaps (iODNcaps, “iSG3caps” in this study) was evaluated using an atopic dermatitis mouse model to visually monitor disease course. Administration of iSG3caps improved skin lesions and decreased epidermal thickness. Underlying this effect is the ability of iSG3 to bind to and prevent phosphorylation of signal transducer and activator of transcription 6, thereby blocking the interleukin-4 signaling cascade mediated by binding of allergens to type 2 helper T cells. The results of our iSG3cap oral delivery experiments suggest that iSG3 may be useful for treating allergic diseases.
机译:在这里,我们报告针对肠道Peyer贴片(PPs)的简单且低成本的口服寡聚脱氧核苷酸(ODN)递送系统。该系统仅需要Dulbecco改良的Eagle培养基,氯化钙,ODN和基本的实验室设备。 ODN纳米胶囊(ODNcaps)通过口服直接递送至PPs,并被PPs中的巨噬细胞吸收,从而诱导免疫反应。使用特应性皮炎小鼠模型通过肉眼监测病程,评估了长期连续口服抑制/抑制性ODNcaps(本研究中为iODNcaps,“ iSG3caps”)的剂量。施用iSG3caps可改善皮肤损伤并降低表皮厚度。该作用的基础是iSG3结合并防止信号转导子和转录激活子6磷酸化的能力,从而阻止了变应原与2型辅助T细胞结合介导的白介素4信号级联反应。我们的iSG3cap口服递送实验的结果表明,iSG3可能对治疗过敏性疾病有用。

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