Exploiting virus-like particles as innovative vaccines against emerging viral infections
被引:66
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作者:
Jeong, Hotcherl
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Ewha Womans Univ, Dept Pharm, Seoul 03760, South KoreaEwha Womans Univ, Dept Pharm, Seoul 03760, South Korea
Jeong, Hotcherl
[1
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Seong, Baik Lin
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Yonsei Univ, Dept Biotechnol, Seoul 03722, South Korea
Yonsei Univ, Vaccine Translat Res Ctr, Seoul 03722, South KoreaEwha Womans Univ, Dept Pharm, Seoul 03760, South Korea
Seong, Baik Lin
[2
,3
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机构:
[1] Ewha Womans Univ, Dept Pharm, Seoul 03760, South Korea
[2] Yonsei Univ, Dept Biotechnol, Seoul 03722, South Korea
[3] Yonsei Univ, Vaccine Translat Res Ctr, Seoul 03722, South Korea
Emerging viruses pose a major threat to humans and livestock with global public health and economic burdens. Vaccination remains an effective tool to reduce this threat, and yet, the conventional cell culture often fails to produce sufficient vaccine dose. As an alternative to cell-culture based vaccine, virus-like particles (VLPs) are considered as a highpriority vaccine strategy against emerging viruses. VLPs represent highly ordered repetitive structures via macromolecular assemblies of viral proteins. The particulate nature allows efficient uptake into antigen presenting cells stimulating both innate and adaptive immune responses towards enhanced vaccine efficacy. Increasing research activity and translation opportunity necessitate the advances in the design of VLPs and new bioprocessing modalities for efficient and cost-effective production. Herein, we describe major achievements and challenges in this endeavor, with respect to designing strategies to harnessing the immunogenic potential, production platforms, downstream processes, and some exemplary cases in developing VLP-based vaccines.
机构:
Arizona State Univ, Ctr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Univ Arizona, Coll Med, Dept Basic Med Sci, Phoenix, AZ 85004 USAArizona State Univ, Ctr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Herbst-Kralovetz, Melissa
Mason, Hugh S.
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Arizona State Univ, Ctr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Arizona State Univ, Sch Life Sci, Tempe, AZ 85287 USAArizona State Univ, Ctr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Mason, Hugh S.
Chen, Qiang
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Arizona State Univ, Ctr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Arizona State Univ, Dept Appl Biol Sci, Mesa, AZ 85212 USAArizona State Univ, Ctr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA