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Neutralization of SARS-CoV-2 variants by rVSV-ΔG-spike-elicited human sera
Yfat Yahalom-Ronen; Noam Erez; Morly Fisher; Hadas Tamir; Boaz Politi; Hagit Achdout; Sharon Melamed; Itai Glinert; Shay Weiss; Inbar Cohen-Gihon; Ofir Israely; Marina Izak; Michal Mandelboim; Yoseph Caraco; Noa Madar-Balakirski; Adva Mechaly; Eilat Shinar; Ran Zichel; Daniel Cohen; Adi Beth-Din; Anat Zvi; Hadar Marcus; Tomer Israely; Nir Paran.
Affiliation
  • Yfat Yahalom-Ronen; Israel Institute for Biological Research
  • Noam Erez; Israel Institute for Biological Research
  • Morly Fisher; Israel Institute for Biological Research
  • Hadas Tamir; Israel Institute for Biological Research
  • Boaz Politi; Israel Institute for Biological Research
  • Hagit Achdout; Israel Institute for Biological Research
  • Sharon Melamed; Israel Institute for Biological Research
  • Itai Glinert; Israel Institute for Biological Research
  • Shay Weiss; Israel Institute for Biological Research
  • Inbar Cohen-Gihon; Israel Institute for Biological Research
  • Ofir Israely; Israel Institute for Biological Research
  • Marina Izak; MDA
  • Michal Mandelboim; Sheba Medical Center
  • Yoseph Caraco; Hadassah Medical Center
  • Noa Madar-Balakirski; Israel Institute for Biological Research
  • Adva Mechaly; Israel Institute for Biological Research
  • Eilat Shinar; MDA
  • Ran Zichel; Israel Institute for Biological Research
  • Daniel Cohen; Tel Aviv University
  • Adi Beth-Din; Israel Institute for Biological Research
  • Anat Zvi; Israel Institute for Biological Research
  • Hadar Marcus; Israel Institute for Biological Research
  • Tomer Israely; Israel Institute for Biological Research
  • Nir Paran; Israel Institute for Biological Research
Preprint in En | PREPRINT-MEDRXIV | ID: ppmedrxiv-21266673
ABSTRACT
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 at specific amino acids that might impede vaccine efficacy. BriLife(R) (rVSV-{Delta}G-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. rVSV-{Delta}G-spike contains several spontaneously-acquired spike mutations that correspond to SARS-CoV-2 variants mutations. We show that human sera from BriLife(R) vaccinees preserve comparable neutralization titers towards alpha, gamma and delta variants, and show less than 3-fold reduction in neutralization capacity of beta and omicron compared to the original virus. Taken together, we show that human sera from BriLife(R) vaccinees overall maintain neutralizing antibody response against all tested variants. We suggest that BriLife(R) acquired mutations may prove advantageous against future SARS-CoV-2 VOCs.
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Full text: 1 Collection: 09-preprints Database: PREPRINT-MEDRXIV Type of study: Prognostic_studies Language: En Year: 2021 Type: Preprint
Full text: 1 Collection: 09-preprints Database: PREPRINT-MEDRXIV Type of study: Prognostic_studies Language: En Year: 2021 Type: Preprint