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Neutralization of SARS-CoV-2 Variants by rVSV-ΔG-Spike-Elicited Human Sera
by
Tamir, Hadas
, Achdout, Hagit
, Paran, Nir
, Fisher, Morly
, Politi, Boaz
, Zichel, Ran
, Cohen-Gihon, Inbar
, Weiss, Shay
, Izak, Marina
, Mandelboim, Michal
, Mechaly, Adva
, Erez, Noam
, Madar-Balakirski, Noa
, Cohen, Daniel
, Marcus, Hadar
, Beth-Din, Adi
, Melamed, Sharon
, Israely, Tomer
, Yahalom-Ronen, Yfat
, Glinert, Itai
, Israeli, Ofir
, Shinar, Eilat
, Caraco, Yoseph
, Zvi, Anat
in
Amino acids
/ Antibodies
/ Antibody response
/ Bioinformatics
/ Brief Report
/ BriLife
/ Clinical trials
/ Coronaviruses
/ COVID-19
/ COVID-19 vaccines
/ Genomes
/ Infections
/ Mutation
/ Neutralization
/ Pandemics
/ Proteins
/ SARS-CoV-2
/ Severe acute respiratory syndrome coronavirus 2
/ Software
/ Stomatitis
/ vaccine
/ Vaccine efficacy
/ Vaccines
/ variants
/ Viral diseases
/ Viruses
/ VOC
2022
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Neutralization of SARS-CoV-2 Variants by rVSV-ΔG-Spike-Elicited Human Sera
by
Tamir, Hadas
, Achdout, Hagit
, Paran, Nir
, Fisher, Morly
, Politi, Boaz
, Zichel, Ran
, Cohen-Gihon, Inbar
, Weiss, Shay
, Izak, Marina
, Mandelboim, Michal
, Mechaly, Adva
, Erez, Noam
, Madar-Balakirski, Noa
, Cohen, Daniel
, Marcus, Hadar
, Beth-Din, Adi
, Melamed, Sharon
, Israely, Tomer
, Yahalom-Ronen, Yfat
, Glinert, Itai
, Israeli, Ofir
, Shinar, Eilat
, Caraco, Yoseph
, Zvi, Anat
in
Amino acids
/ Antibodies
/ Antibody response
/ Bioinformatics
/ Brief Report
/ BriLife
/ Clinical trials
/ Coronaviruses
/ COVID-19
/ COVID-19 vaccines
/ Genomes
/ Infections
/ Mutation
/ Neutralization
/ Pandemics
/ Proteins
/ SARS-CoV-2
/ Severe acute respiratory syndrome coronavirus 2
/ Software
/ Stomatitis
/ vaccine
/ Vaccine efficacy
/ Vaccines
/ variants
/ Viral diseases
/ Viruses
/ VOC
2022
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Neutralization of SARS-CoV-2 Variants by rVSV-ΔG-Spike-Elicited Human Sera
by
Tamir, Hadas
, Achdout, Hagit
, Paran, Nir
, Fisher, Morly
, Politi, Boaz
, Zichel, Ran
, Cohen-Gihon, Inbar
, Weiss, Shay
, Izak, Marina
, Mandelboim, Michal
, Mechaly, Adva
, Erez, Noam
, Madar-Balakirski, Noa
, Cohen, Daniel
, Marcus, Hadar
, Beth-Din, Adi
, Melamed, Sharon
, Israely, Tomer
, Yahalom-Ronen, Yfat
, Glinert, Itai
, Israeli, Ofir
, Shinar, Eilat
, Caraco, Yoseph
, Zvi, Anat
in
Amino acids
/ Antibodies
/ Antibody response
/ Bioinformatics
/ Brief Report
/ BriLife
/ Clinical trials
/ Coronaviruses
/ COVID-19
/ COVID-19 vaccines
/ Genomes
/ Infections
/ Mutation
/ Neutralization
/ Pandemics
/ Proteins
/ SARS-CoV-2
/ Severe acute respiratory syndrome coronavirus 2
/ Software
/ Stomatitis
/ vaccine
/ Vaccine efficacy
/ Vaccines
/ variants
/ Viral diseases
/ Viruses
/ VOC
2022
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Neutralization of SARS-CoV-2 Variants by rVSV-ΔG-Spike-Elicited Human Sera
Journal Article
Neutralization of SARS-CoV-2 Variants by rVSV-ΔG-Spike-Elicited Human Sera
2022
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Overview
The emergence of rapidly spreading variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) poses a major challenge to the ability of vaccines and therapeutic antibodies to provide immunity. These variants contain mutations of specific amino acids that might impede vaccine efficacy. BriLife® (rVSV-ΔG-spike) is a newly developed SARS-CoV-2 vaccine candidate currently in phase II clinical trials. It is based on a replication-competent vesicular stomatitis virus (VSV) platform. The rVSV-ΔG-spike contains several spontaneously acquired spike mutations that correspond to SARS-CoV-2 variants’ mutations. We show that human sera from BriLife® vaccinees preserve comparable neutralization titers towards alpha, gamma, and delta variants and show less than a three-fold reduction in the neutralization capacity of beta and omicron compared to the original virus. Taken together, we show that human sera from BriLife® vaccinees overall maintain a neutralizing antibody response against all tested variants. We suggest that BriLife®-acquired mutations may prove advantageous against future SARS-CoV-2 VOCs.
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