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10.3390/vaccines10020291

http://scihub22266oqcxt.onion/10.3390/vaccines10020291
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35214749!8879449!35214749
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suck abstract from ncbi


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pmid35214749      Vaccines+(Basel) 2022 ; 10 (2): ä
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  • Neutralization of SARS-CoV-2 Variants by rVSV-DeltaG-Spike-Elicited Human Sera #MMPMID35214749
  • Yahalom-Ronen Y; Erez N; Fisher M; Tamir H; Politi B; Achdout H; Melamed S; Glinert I; Weiss S; Cohen-Gihon I; Israeli O; Izak M; Mandelboim M; Caraco Y; Madar-Balakirski N; Mechaly A; Shinar E; Zichel R; Cohen D; Beth-Din A; Zvi A; Marcus H; Israely T; Paran N
  • Vaccines (Basel) 2022[Feb]; 10 (2): ä PMID35214749show ga
  • 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((R)) (rVSV-DeltaG-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-DeltaG-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 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((R)) vaccinees overall maintain a 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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