Double-layered protein nanoparticles induce broad protection against divergent influenza A viruses

被引:158
作者
Deng, Lei [1 ]
Mohan, Teena [1 ]
Chang, Timothy Z. [2 ]
Gonzalez, Gilbert X. [1 ]
Wang, Ye [1 ]
Kwon, Young-Man [1 ]
Kang, Sang-Moo [1 ]
Compans, Richard W. [3 ,4 ]
Champion, Julie A. [2 ]
Wang, Bao-Zhong [1 ]
机构
[1] Georgia State Univ, Ctr Inflammat Immun & Infect, Atlanta, GA 30303 USA
[2] Georgia State Univ, Sch Chem & Biomol Engn, Atlanta, GA 30332 USA
[3] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[4] Emory Univ, Sch Med, Emory Vaccine Ctr, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
HEMAGGLUTININ-STEM; MONOCLONAL-ANTIBODY; ESCHERICHIA-COLI; MATRIX PROTEIN-2; HUMAN INFECTION; DOMAIN; VACCINATION; ACTIVATION; IMMUNOGEN; VACCINES;
D O I
10.1038/s41467-017-02725-4
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
Current influenza vaccines provide limited protection against circulating influenza A viruses. A universal influenza vaccine will eliminate the intrinsic limitations of the seasonal flu vaccines. Here we report methodology to generate double-layered protein nanoparticles as a universal influenza vaccine. Layered nanoparticles are fabricated by desolvating tetrameric M2e into protein nanoparticle cores and coating these cores by crosslinking headless HAs. Representative headless HAs of two HA phylogenetic groups are constructed and purified. Vaccinations with the resulting protein nanoparticles in mice induces robust long-lasting immunity, fully protecting the mice against challenges by divergent influenza A viruses of the same group or both groups. The results demonstrate the importance of incorporating both structure-stabilized HA stalk domains and M2e into a universal influenza vaccine to improve its protective potency and breadth. These potent disassemblable protein nanoparticles indicate a wide application in protein drug delivery and controlled release.
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页数:12
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