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Newcastle Disease Virus-Like Particles Displaying Prefusion-Stabilized SARS-CoV-2 Spikes Elicit Potent Neutralizing Responses.

Authors :
Yang Y
Shi W
Abiona OM
Nazzari A
Olia AS
Ou L
Phung E
Stephens T
Tsybovsky Y
Verardi R
Wang S
Werner A
Yap C
Ambrozak D
Bylund T
Liu T
Nguyen R
Wang L
Zhang B
Zhou T
Chuang GY
Graham BS
Mascola JR
Corbett KS
Kwong PD
Source :
Vaccines [Vaccines (Basel)] 2021 Jan 21; Vol. 9 (2). Date of Electronic Publication: 2021 Jan 21.
Publication Year :
2021

Abstract

The COVID-19 pandemic highlights an urgent need for vaccines that confer protection from SARS-CoV-2 infection. One approach to an effective COVID-19 vaccine may be through the display of SARS-CoV-2 spikes on the surface of virus-like particles, in a manner structurally mimicking spikes on a native virus. Here we report the development of Newcastle disease virus-like particles (NDVLPs) displaying the prefusion-stabilized SARS-CoV-2 spike ectodomain (S2P). Immunoassays with SARS-CoV-2-neutralizing antibodies revealed the antigenicity of S2P-NDVLP to be generally similar to that of soluble S2P, and negative-stain electron microscopy showed S2P on the NDVLP surface to be displayed with a morphology corresponding to its prefusion conformation. Mice immunized with S2P-NDVLP showed substantial neutralization titers (geometric mean ID <subscript>50</subscript> = 386) two weeks after prime immunization, significantly higher than those elicited by a molar equivalent amount of soluble S2P (geometric mean ID <subscript>50</subscript> = 17). Neutralizing titers at Week 5, two weeks after a boost immunization with S2P-NDVLP doses ranging from 2.0 to 250 μg, extended from 2125 to 4552, and these generally showed a higher ratio of neutralization versus ELISA than observed with soluble S2P. Overall, S2P-NDVLP appears to be a promising COVID-19 vaccine candidate capable of eliciting substantial neutralizing activity.

Details

Language :
English
ISSN :
2076-393X
Volume :
9
Issue :
2
Database :
MEDLINE
Journal :
Vaccines
Publication Type :
Academic Journal
Accession number :
33494381
Full Text :
https://doi.org/10.3390/vaccines9020073