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用H5N1疫苗加聚肌苷酸:聚胞苷酸12尿苷(一种Toll样受体激动剂)进行鼻内免疫,可保护小鼠免受同源和异源病毒攻击。

Intranasal immunization with H5N1 vaccine plus Poly I:Poly C12U, a Toll-like receptor agonist, protects mice against homologous and heterologous virus challenge.

作者信息

Ichinohe Takeshi, Kawaguchi Akira, Tamura Shin-ichi, Takahashi Hidehiro, Sawa Hirofumi, Ninomiya Ai, Imai Masaki, Itamura Shigeyuki, Odagiri Takato, Tashiro Masato, Chiba Joe, Sata Tetsutaro, Kurata Takeshi, Hasegawa Hideki

机构信息

Department of Pathology, National Institute of Infectious Diseases, 4-7-1 Gakuen, Musashimurayama-shi, Tokyo 208-0011, Japan.

出版信息

Microbes Infect. 2007 Sep;9(11):1333-40. doi: 10.1016/j.micinf.2007.06.007. Epub 2007 Jul 1.

Abstract

The avian H5N1 influenza virus has the potential to cause a new pandemic. Since it is difficult to predict which strain of influenza will cause a pandemic, it is advantageous to produce vaccines that confer cross-protective immunity. Mucosal vaccine administration was reported to induce cross-protective immunity by inducing secretion of IgA at the mucosal surface. Adjuvants can also enhance the development of fully protective mucosal immunity. Here we show that a new mucosal adjuvant, poly I:poly C12U (Ampligen), a Toll-like receptor 3 agonist proven to be safe in a Phase III human trial, is an effective adjuvant for H5N1 influenza vaccination. Intranasal administration of a candidate influenza vaccine with Ampligen resulted in secretion of IgA, and protected mice that were subsequently challenged with homologous A/Vietnam/1194/2004 and heterologous A/HK/483/97 and A/Indonesia/6/2005 virus.

摘要

禽H5N1流感病毒有可能引发一场新的大流行。由于很难预测哪种流感毒株会引发大流行,生产具有交叉保护免疫力的疫苗是有利的。据报道,黏膜疫苗接种可通过诱导黏膜表面IgA的分泌来诱导交叉保护免疫力。佐剂也可以增强完全保护性黏膜免疫的发展。在此我们表明,一种新的黏膜佐剂,聚肌苷酸:聚胞苷酸12U(Ampligen),一种在III期人体试验中已证明安全的Toll样受体3激动剂,是H5N1流感疫苗接种的有效佐剂。用Ampligen鼻内接种候选流感疫苗导致了IgA的分泌,并保护小鼠免受随后同源的A/越南/1194/2004以及异源的A/香港/483/97和A/印度尼西亚/6/2005病毒的攻击。

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