| Title | PolyI:polyC(12)U adjuvant-combined intranasal vaccine protects mice against highly pathogenic H5N1 influenza virus variants. | | Author(s) | Ichinohe T, Ainai A, Tashiro M, Sata T, Hasegawa H | | Institution | Department of Pathology, National Institute of Infectious Diseases, 4-7-1 Gakuen, Musashimurayama-shi, Tokyo, Japan; Department of Immunobiology, Yale University School of Medicine, 300 Cedar Street, TAC S640, New Haven, CT, USA. | | Source | Vaccine 2009 Oct 23; 27(45):6276-9. | | Abstract | The highly pathogenic avian H5N1 influenza virus has the potential to incite a global pandemic. Therefore, there is an urgent need to develop effective vaccines against these viruses. Because it is difficult to predict which strain of influenza will cause a pandemic, it is advantageous to develop vaccines that will confer cross-protective immunity against variants of the influenza virus. Recently, we reported that the Toll-like receptor 3 agonist, polyI:polyC(12)U (Ampligen((R))), has been proven to be safe in a Phase III human trial, and is an effective mucosal adjuvant for intranasal H5N1 influenza vaccination. Intranasal administration of an Ampligen((R)) adjuvanted pre-pandemic H5N1 vaccine (NIBRG14), which was derived from the A/Vietnam/1194/2004 strain, resulted in the secretion of vaccine-specific IgA and IgG in nasal mucosa and serum, respectively, and protected mice against homologous A/Vietnam/1194/2004 and heterologous A/Hong Kong/483/97 and A/Indonesia/6/2005 viral challenge. | | Language | eng | | Pub Type(s) | Journal Article
| | PubMed ID | 19840660 |
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