Crossprotection induced by virus-like particles containing influenza dual-hemagglutinin and M2 ectodomain

被引:0
|
作者
Mao, Jie [1 ]
Eom, Gi-Deok [1 ]
Yoon, Keon-Woong [1 ]
Kim, Min-Ju [1 ]
Chu, Ki-Back [2 ]
Kang, Hae-Ji [3 ]
Quan, Fu-Shi [2 ,4 ]
机构
[1] Kyung Hee Univ, Grad Sch, Dept Biomed Sci, Seoul 02447, South Korea
[2] Kyung Hee Univ, Biomed Sci Inst, Core Res Inst CRI, Med Res Ctr Bioreact React Oxygen Species, Seoul 02447, South Korea
[3] Georgia State Univ, Inst Biomed Sci, Ctr Translat Antiviral Res, Atlanta, GA 30303 USA
[4] Kyung Hee Univ, Sch Med, Dept Med Zool, Seoul 02447, South Korea
基金
新加坡国家研究基金会;
关键词
hemagglutinin; influenza virus; M2e5x; universal vaccine; virus-like particles; CROSS-PROTECTION; VACCINE; MICE; H1N1; INFECTION; IMMUNITY; SUBTYPES;
D O I
10.2217/nnm-2023-0353
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: To develop an effective universal vaccine against antigenically different influenza viruses. Materials & methods: We generated influenza virus-like particles (VLPs) expressing the H1 and H3 antigens with or without M2e5x. VLP-induced immune responses and crossprotection against H1N1, H3N2 or H5N1 viruses were assessed to evaluate their protective efficacy. Results: H1H3M2e5x immunization elicited higher crossreactive IgG antibodies than H1H3 VLPs. Upon challenge, both VLPs enhanced lung IgG, IgA and germinal center B-cell responses compared with control. While these VLPs conferred protection, H1H3M2e5x showed greater lung viral load reduction than H1H3 VLPs with minimal body weight loss. Conclusion: Utilizing VLPs containing dual-hemagglutinin, along with M2e5x, can be a vaccination strategy for inducing crossprotection against influenza A viruses. [GRAPHICS] .
引用
收藏
页码:741 / 754
页数:14
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