Adjuvants and Immunization Strategies to Induce Influenza Virus Hemagglutinin Stalk Antibodies

被引:54
作者
Goff, Peter H. [1 ,2 ]
Eggink, Dirk [1 ]
Seibert, Christopher W. [1 ,2 ]
Hai, Rong [1 ]
Martinez-Gil, Luis [1 ]
Krammer, Florian [1 ]
Palese, Peter [1 ,3 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Microbiol, New York, NY USA
[2] Icahn Sch Med Mt Sinai, Grad Sch Biomed Sci, New York, NY USA
[3] Icahn Sch Med Mt Sinai, Dept Med, New York, NY USA
来源
PLOS ONE | 2013年 / 8卷 / 11期
基金
奥地利科学基金会; 美国国家卫生研究院;
关键词
VIRAL-INFECTION; VACCINE; IGA; MECHANISM; RESPONSES; IMMUNITY;
D O I
10.1371/journal.pone.0079194
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The global population remains vulnerable in the face of the next pandemic influenza virus outbreak, and reformulated vaccinations are administered annually to manage seasonal epidemics. Therefore, development of a new generation of vaccines is needed to generate broad and persistent immunity to influenza viruses. Here, we describe three adjuvants that enhance the induction of stalk-directed antibodies against heterologous and heterosubtypic influenza viruses when administered with chimeric HA proteins. Addavax, an MF59-like nanoemulsion, poly(I: C), and an RNA hairpin derived from Sendai virus (SeV) Cantell were efficacious intramuscularly. The SeV RNA and poly(I: C) also proved to be effective respiratory mucosal adjuvants. Although the quantity and quality of antibodies induced by the adjuvants varied, immunized mice demonstrated comparable levels of protection against challenge with influenza A viruses on the basis of HA stalk reactivity. Finally, we present that intranasally, but not intramuscularly, administered chimeric HA proteins induce mucosal IgA antibodies directed at the HA stalk.
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页数:11
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