首页> 外文会议>Nanotechnology in medicine II: briding translational in vitro and in vivo interfaces >NANOMEDICINES FOR THE TREATMENT OF AUTOIMMUNE INFLAMMATION: ENGINEERING DESIGN, MECHANISMS AND DISEASES
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NANOMEDICINES FOR THE TREATMENT OF AUTOIMMUNE INFLAMMATION: ENGINEERING DESIGN, MECHANISMS AND DISEASES

机译:用于治疗自发炎症的纳米技术:工程设计,机理和疾病

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The complexity of autoimmune diseases is a barrier to the design of strategies that can blunt autoimmunity without impairing general immunity. We have shown that systemic delivery of nanoparticles (NPs) coated with autoimmune disease-relevant peptide-major-histocompatibility-complex (pMHC) molecules triggers the formation and profound expansion of antigen-specific T-regulatory T-cells in different mouse models, including mice humanized with lymphocytes from patients, leading to resolution of a broad range of established autoimmune phenomena. I will highlight the engineering principles impacting biological activity, will illustrate how these nanomedicines interact with cognate T-cells and will describe the pharmacokinetic behavior and toxicological profile of this novel class of drugs, potentially useful for treating a broad spectrum of autoimmune conditions in a disease-specific manner.
机译:自身免疫性疾病的复杂性是设计策略的障碍,该策略可以钝化自身免疫而不损害一般免疫。我们已经显示,全身递送的纳米颗粒(NPs)涂有自身免疫性疾病相关肽-主要组织相容性复合物(pMHC)分子会触发抗原特异性T调节性T细胞在不同小鼠模型中的形成和深度扩展,包括用来自患者的淋巴细胞进行人源化的小鼠,导致广泛的已建立的自身免疫现象得以解决。我将重点介绍影响生物活性的工程原理,阐述这些纳米药物如何与同源T细胞相互作用,并描述这种新型药物的药代动力学行为和毒理学特征,可能对治疗疾病中的多种自身免疫性疾病有用特定的方式。

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