Suppr超能文献

一种新型基于肽的疫苗候选物,在小鼠模型中具有针对流感 A 的保护效力。

A novel peptide-based vaccine candidate with protective efficacy against influenza A in a mouse model.

机构信息

Department of Medical Microbiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Bionor Pharma AS, P.O. Box 1477 Vika, NO-0116 Oslo, Norway.

出版信息

Virology. 2018 Feb;515:21-28. doi: 10.1016/j.virol.2017.11.018. Epub 2017 Dec 7.

Abstract

Current influenza vaccines mainly induce antibody responses to the variable hemagglutinin proteins of the virus strains included in the vaccine. Instead, a broadly protective influenza vaccine should aim at inducing antibody- and/or cell-mediated immunity against conserved viral proteins. Vacc-FLU is a peptide based vaccine combining conserved B and T cell epitopes. Peptide selection was done using a proprietary peptide design platform technology focusing on responses to human leukocyte antigen (HLA)-restricted epitopes. Immunization of wild-type mice and mice transgenic for HLA-A2.1 with the peptide mix successfully induced both humoral and cell mediated immune responses. Partial protection from severe weight loss upon challenge was observed in both mouse strains but was stronger and observed at lower vaccine doses in transgenic mice. Our results show that the Vacc-FLU peptide mix is capable of inducing IFNγ-producing T cells and antibody-producing B cells which can protect from severe disease symptoms upon infection.

摘要

目前的流感疫苗主要诱导针对疫苗中包含的病毒株的可变血凝素蛋白的抗体反应。相反,广泛保护性的流感疫苗应该旨在诱导针对保守病毒蛋白的抗体和/或细胞介导免疫。Vacc-FLU 是一种基于肽的疫苗,结合了保守的 B 细胞和 T 细胞表位。肽的选择是使用专有的肽设计平台技术完成的,该技术专注于对人类白细胞抗原 (HLA)-受限表位的反应。用肽混合物对野生型小鼠和 HLA-A2.1 转基因小鼠进行免疫接种,成功地诱导了体液和细胞介导的免疫反应。在两种小鼠品系中都观察到对严重体重减轻的部分保护,但在转基因小鼠中,保护作用更强,并且在较低的疫苗剂量下即可观察到。我们的结果表明,Vacc-FLU 肽混合物能够诱导产生 IFNγ的 T 细胞和产生抗体的 B 细胞,从而在感染时防止严重的疾病症状。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验