Neutralization of SARS-CoV-2 Variants by rVSV-ΔG-Spike-Elicited Human Sera.
Yfat Yahalom-RonenNoam ErezMorly FisherHadas TamirBoaz PolitiHagit AchdoutSharon MelamedItai GlinertShay WeissInbar Cohen-GihonOfir IsraeliMarina IzakMichal MandelboimYoseph CaracoNoa Madar-BalakirskiAdva MechalyEilat ShinarRan ZichelDaniel CohenAdi Beth-DinAnat ZviHadar MarcusTomer IsraelyNir ParanPublished in: Vaccines (2022)
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.