Hemagglutinin-based polyanhydride nanovaccines against H5NI influenza elicit protective virus neutralizing titers and cell-mediated immunity

被引:40
|
作者
Ross, Kathleen A. [1 ]
Loyd, Hyelee [1 ]
Wu, Wuwei [1 ]
Huntimer, Lucas [1 ]
Ahmed, Shaheen [2 ]
Sambol, Anthony [2 ]
Broderick, Scott [1 ]
Flickinger, Zachary [1 ]
Rajan, Krishna [1 ]
Bronich, Tatiana [2 ]
Mallapragada, Surya [1 ]
Wannemuehler, Michael J. [1 ]
Carpenter, Susan [1 ]
Narasimhan, Balaji [1 ]
机构
[1] Iowa State Univ, Ames, IA 50011 USA
[2] Univ Nebraska Med Ctr, Omaha, NE USA
来源
INTERNATIONAL JOURNAL OF NANOMEDICINE | 2015年 / 10卷
关键词
polymer; nanoparticle; vaccine; subunit; neutralizing antibody; MICROSPHERES; IMMUNIZATION; DESIGN; MICE;
D O I
10.2147/IJN.S72264
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
H5N1 avian influenza is a significant global concern with the potential to become the next pandemic threat. Recombinant subunit vaccines are an attractive alternative for pandemic vaccines compared to traditional vaccine technologies. In particular, polyanhydride nanoparticles encapsulating subunit proteins have been shown to enhance humoral and cell-mediated immunity and provide protection upon lethal challenge. In this work, a recombinant H5 hemagglutinin trimer (H5(3)) was produced and encapsulated into polyanhydride nanoparticles. The studies performed indicated that the recombinant H5(3) antigen was a robust immunogen. Immunizing mice with H5(3) encapsulated into polyanhydride nanoparticles induced high neutralizing antibody titers and enhanced CD4(+) T cell recall responses in mice. Finally, the H5(3)-based polyanhydride nanovaccine induced protective immunity against a low-pathogenic H5N1 viral challenge. Informatics analyses indicated that mice receiving the nanovaccine formulations and subsequently challenged with virus were similar to naive mice that were not challenged. The current studies provide a basis to further exploit the advantages of polyanhydride nanovaccines in pandemic scenarios.
引用
收藏
页码:229 / 243
页数:15
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