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
Department of Pathology, National Institute of Infectious Diseases, 4-7-1 Gakuen, Musashimurayama-shi, Tokyo 208-0011, Japan.
Microbes Infect. 2007 Sep;9(11):1333-40. doi: 10.1016/j.micinf.2007.06.007. Epub 2007 Jul 1.
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.
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。