Mosaic quadrivalent influenza vaccine single nanoparticle characterization

被引:0
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作者
Rong Sylvie Yang
Maria Traver
Nathan Barefoot
Tyler Stephens
Casper Alabanza
Javier Manzella-Lapeira
Guozhang Zou
Jeremy Wolff
Yile Li
Melissa Resto
William Shadrick
Yanhong Yang
Vera B. Ivleva
Yaroslav Tsybovsky
Kevin Carlton
Joseph Brzostowski
Jason G. Gall
Q. Paula Lei
机构
[1] National Institutes of Health,Vaccine Production Program, Vaccine Research Center, National Institute of Allergy and Infectious Diseases
[2] LIG,Twinbrook Imaging Facility
[3] NIAID,Vaccine Research Center Electron Microscopy Unit, Cancer Research Technology Program, Leidos Biomedical Research, Inc.
[4] NIH,undefined
[5] Frederick National Laboratory for Cancer Research,undefined
来源
Scientific Reports | / 14卷
关键词
Fluorescence imaging; TIRFM; Fluorescent labeling; Size-exclusion chromatography; ELISA; Mass spectrometry; Influenza vaccine; Nanoparticle;
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摘要
Recent work by our laboratory and others indicates that co-display of multiple antigens on protein-based nanoparticles may be key to induce cross-reactive antibodies that provide broad protection against disease. To reach the ultimate goal of a universal vaccine for seasonal influenza, a mosaic influenza nanoparticle vaccine (FluMos-v1) was developed for clinical trial (NCT04896086). FluMos-v1 is unique in that it is designed to co-display four recently circulating haemagglutinin (HA) strains; however, current vaccine analysis techniques are limited to nanoparticle population analysis, thus, are unable to determine the valency of an individual nanoparticle. For the first time, we demonstrate by total internal reflection fluorescence microscopy and supportive physical–chemical methods that the co-display of four antigens is indeed achieved in single nanoparticles. Additionally, we have determined percentages of multivalent (mosaic) nanoparticles with four, three, or two HA proteins. The integrated imaging and physicochemical methods we have developed for single nanoparticle multivalency will serve to further understand immunogenicity data from our current FluMos-v1 clinical trial.
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