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用热不稳定毒素突变体进行全身免疫或黏膜与全身免疫联合后,对流感病毒鼻内攻击具有长期保护作用。

Prolonged protection against Intranasal challenge with influenza virus following systemic immunization or combinations of mucosal and systemic immunizations with a heat-labile toxin mutant.

作者信息

Zhou Fengmin, Goodsell Amanda, Uematsu Yasushi, Vajdy Michael

机构信息

Novartis Vaccines and Diagnostics, Inc., Emeryville, California, USA.

出版信息

Clin Vaccine Immunol. 2009 Apr;16(4):471-8. doi: 10.1128/CVI.00311-08. Epub 2009 Feb 4.

Abstract

Seasonal influenza virus infections cause considerable morbidity and mortality in the world, and there is a serious threat of a pandemic influenza with the potential to cause millions of deaths. Therefore, practical influenza vaccines and vaccination strategies that can confer protection against intranasal infection with influenza viruses are needed. In this study, we demonstrate that using LTK63, a nontoxic mutant of the heat-labile toxin from Escherichia coli, as an adjuvant for both mucosal and systemic immunizations, systemic (intramuscular) immunization or combinations of mucosal (intranasal) and intramuscular immunizations protected mice against intranasal challenge with a lethal dose of live influenza virus at 3.5 months after the second immunization.

摘要

季节性流感病毒感染在全球造成了相当高的发病率和死亡率,并且存在大流行性流感的严重威胁,有可能导致数百万人死亡。因此,需要实用的流感疫苗和接种策略,以提供针对流感病毒鼻内感染的保护。在本研究中,我们证明,使用大肠杆菌不耐热毒素的无毒突变体LTK63作为粘膜和全身免疫的佐剂,全身(肌肉内)免疫或粘膜(鼻内)和肌肉内免疫的组合,在第二次免疫后3.5个月可保护小鼠免受致死剂量的活流感病毒鼻内攻击。

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