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基于CpG寡脱氧核苷酸的疫苗佐剂配方的研发。

Development of CpG ODN Based Vaccine Adjuvant Formulations.

作者信息

Gursel Mayda, Gursel Ihsan

机构信息

Department of Biological Sciences, Middle East Technical University, 06800, Ankara, Turkey.

THORLAB-Therapeutic Oligonucleotide Research Laboratory, Department of Molecular Biology and Genetics, Bilkent University, Bilkent, 06800, Ankara, Turkey.

出版信息

Methods Mol Biol. 2016;1404:289-298. doi: 10.1007/978-1-4939-3389-1_20.

Abstract

Development of effective vaccine mediated immune responses relies on the use of vaccine adjuvants capable of enhancing and directing the adaptive immune response to the antigen. When used as vaccine adjuvants, type I interferon inducing agents can elicit potent effector/memory T cell responses and humoral immunity. Distinct sequences of single stranded synthetic oligodeoxynucleotides containing unmethylated cytosine-phosphate-guanine oligodeoxynucleotide motifs (CpG ODN) can generate type I interferon production via a TLR9-MyD88-IRF7-mediated signaling pathway. Here, we describe two different methods of preparing CpG ODN-based vaccine adjuvant formulations that can induce a robust IFNα response from human peripheral blood mononuclear cells.

摘要

有效的疫苗介导免疫反应的发展依赖于使用能够增强和引导对抗原的适应性免疫反应的疫苗佐剂。当用作疫苗佐剂时,I型干扰素诱导剂可引发有效的效应/记忆T细胞反应和体液免疫。含有未甲基化胞嘧啶-磷酸-鸟嘌呤寡脱氧核苷酸基序(CpG ODN)的单链合成寡脱氧核苷酸的不同序列可通过TLR9-MyD88-IRF7介导的信号通路产生I型干扰素。在此,我们描述了两种不同的制备基于CpG ODN的疫苗佐剂制剂的方法,这些制剂可诱导人外周血单个核细胞产生强烈的IFNα反应。

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