病毒学
佐剂
鼻腔给药
免疫
H5N1亚型流感病毒
病毒
抗体
异源的
接种疫苗
生物
甲型流感病毒
流感疫苗
流感减毒活疫苗
医学
免疫学
生物化学
基因
作者
Takeshi Ichinohe,Akira Ainai,Yasushi Ami,Noriyo Nagata,Naoko Iwata,Akira Kawaguchi,Yuriko Suzaki,Takato Odagiri,Masato Tashiro,Hitomi Takahashi,David R. Strayer,William A. Carter,Joe Chiba,Shinichi Tamura,Tetsutaro Sata,Takeshi Kurata,Hideki Hasegawa
摘要
Abstract The effectiveness in cynomolgus macaques of intranasal administration of an influenza A H5N1 pre‐pandemic vaccine combined with synthetic double‐stranded RNA (polyI/polyC12U) as an adjuvant was examined. The monkeys were immunized with the adjuvant‐combined vaccine on weeks 0, 3, and 5, and challenged with the homologous virus 2 weeks after the third immunization. After the second immunization, the immunization induced vaccine‐specific salivary IgA and serum IgG antibodies, as detected by ELISA. The serum IgG antibodies present 2 weeks after the third immunization not only had high neutralizing activity against the homologous virus, they also neutralized significantly heterologous influenza A H5N1 viruses. The vaccinated animals were protected completely from the challenge infection with the homologous virus. These results suggest that intranasal immunization with the Double stranded RNA‐combined influenza A H5N1 vaccine induce mucosal IgA and serum IgG antibodies which could protect humans from homologous influenza A H5N1 viruses which have a pandemic potential. J. Med. Virol. 82:1754–1761, 2010. © 2010 Wiley‐Liss, Inc.
科研通智能强力驱动
Strongly Powered by AbleSci AI