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大流行前用AS03佐剂的H5N1流感疫苗:临床前和临床数据综述

Prepandemic H5N1 influenza vaccine adjuvanted with AS03: a review of the pre-clinical and clinical data.

作者信息

Leroux-Roels Geert

机构信息

Ghent University and Hospital, Center for Vaccinology, Ghent, Belgium.

出版信息

Expert Opin Biol Ther. 2009 Aug;9(8):1057-71. doi: 10.1517/14712590903066695.

Abstract

BACKGROUND

Universal and timely administration of a prepandemic vaccine is considered to be one of the most effective measures to reduce the incidence of pandemic influenza infection and consequently its morbidity and mortality.

OBJECTIVES

To provide the reader with basic insights into influenza virus infections, the threat of a pandemic and the challenges it poses for vaccine development.

METHODS

This review summarizes the reported preclinical and clinical data obtained with the prepandemic H5N1 vaccine adjuvanted with AS03.

RESULTS

The AS03-adjuvanted prepandemic H5N1 influenza vaccine allows for antigen sparing, has a good safety and acceptable reactogenicity profile, induces an immune response that not only meets all European Committee for Medicinal Products (CHMP) and FDA requirements for the vaccine strain but also generates neutralizing antibodies that broadly cross-react against H5N1 drift strains, and finally conveys protection in a ferret model against lethal challenges with homologous and heterologous H5N1 viruses.

摘要

背景

普遍且及时接种大流行前疫苗被认为是降低大流行性流感感染发病率以及由此导致的发病率和死亡率的最有效措施之一。

目的

为读者提供有关流感病毒感染、大流行威胁及其对疫苗研发构成的挑战的基本见解。

方法

本综述总结了使用AS03佐剂的大流行前H5N1疫苗获得的已报道的临床前和临床数据。

结果

AS03佐剂的大流行前H5N1流感疫苗可节省抗原,具有良好的安全性和可接受的反应原性,诱导的免疫反应不仅符合欧洲药品管理局(CHMP)和美国食品药品监督管理局(FDA)对疫苗株的要求,还能产生对H5N1漂移株具有广泛交叉反应的中和抗体,最终在雪貂模型中对同源和异源H5N1病毒的致死性攻击提供保护。

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