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合成DNA疫苗:通过电穿孔和共递送基因佐剂提高疫苗效力。

Synthetic DNA vaccines: improved vaccine potency by electroporation and co-delivered genetic adjuvants.

作者信息

Flingai Seleeke, Czerwonko Matias, Goodman Jonathan, Kudchodkar Sagar B, Muthumani Kar, Weiner David B

机构信息

Department of Pathology and Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania , Philadelphia, PA , USA.

出版信息

Front Immunol. 2013 Nov 4;4:354. doi: 10.3389/fimmu.2013.00354.

Abstract

In recent years, DNA vaccines have undergone a number of technological advancements that have incited renewed interest and heightened promise in the field. Two such improvements are the use of genetically engineered cytokine adjuvants and plasmid delivery via in vivo electroporation (EP), the latter of which has been shown to increase antigen delivery by nearly 1000-fold compared to naked DNA plasmid delivery alone. Both strategies, either separately or in combination, have been shown to augment cellular and humoral immune responses in not only mice, but also in large animal models. These promising results, coupled with recent clinical trials that have shown enhanced immune responses in humans, highlight the bright prospects for DNA vaccines to address many human diseases.

摘要

近年来,DNA疫苗经历了多项技术进步,这激发了该领域新的兴趣并带来了更高的期望。其中两项改进是使用基因工程细胞因子佐剂和通过体内电穿孔(EP)进行质粒递送,与单独的裸DNA质粒递送相比,后者已被证明可将抗原递送增加近1000倍。这两种策略,单独或联合使用,已被证明不仅能增强小鼠,还能增强大型动物模型中的细胞免疫和体液免疫反应。这些令人鼓舞的结果,再加上最近在人类身上显示出增强免疫反应的临床试验,凸显了DNA疫苗应对许多人类疾病的光明前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b83e/3816528/89d3de283642/fimmu-04-00354-g001.jpg

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