4.8 Article

Neutralizing activity of Sputnik V vaccine sera against SARS-CoV-2 variants

Journal

NATURE COMMUNICATIONS
Volume 12, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41467-021-24909-9

Keywords

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Funding

  1. Viral-Host Pathogenesis Training Grant [T32 AI07647]
  2. NRSA [F31 AI154739]
  3. CHOT-SG (Fukuoka University, Japan)
  4. Ministry of Science and Technology (MOST, Taiwan)
  5. NIH [AI123449, AI138921]
  6. Department of Microbiology, Icahn School of Medicine at Mount Sinai
  7. Ward-Coleman estate
  8. Emergent Ventures, an initiative of the Mercatus Center at George Mason University
  9. Office of the Vice Chancellor for Research at LSU Health Sciences Center Shreveport
  10. Ministry of Health (Ministerio de Salud), Argentina
  11. SARS-CoV-2 VSV

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The authors characterize the neutralizing capacity of post-Sputnik V vaccination sera against SARS-CoV-2 variants of concern B.1.1.7 (alpha) and B.1.351 (beta), showing the latter to exhibit resistance to neutralization in vitro.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has infected at least 180 million people since its identification as the cause of the current COVID-19 pandemic. The rapid pace of vaccine development has resulted in multiple vaccines already in use worldwide. The contemporaneous emergence of SARS-CoV-2 'variants of concern' (VOC) across diverse geographic locales underscores the need to monitor the efficacy of vaccines being administered globally. All WHO designated VOC carry spike (S) polymorphisms thought to enable escape from neutralizing antibodies. Here, we characterize the neutralizing activity of post-Sputnik V vaccination sera against the ensemble of S mutations present in alpha (B.1.1.7) and beta (B.1.351) VOC. Using de novo generated replication-competent vesicular stomatitis virus expressing various SARS-CoV-2-S in place of VSV-G (rcVSV-CoV2-S), coupled with a clonal 293T-ACE2+TMPRSS2+cell line optimized for highly efficient S-mediated infection, we determine that only 1 out of 12 post-vaccination serum samples shows effective neutralization (IC90) of rcVSV-CoV2-S: B.1.351 at full serum strength. The same set of sera efficiently neutralize S from B.1.1.7 and exhibit only moderately reduced activity against S carrying the E484K substitution alone. Taken together, our data suggest that control of some emergent SARS-CoV-2 variants may benefit from updated vaccines. Here, the authors characterize the neutralization capacity of post-Sputnik V vaccination sera against SARS-CoV-2 variants of concern B.1.1.7 (alpha) and B.1.351 (beta), showing the latter to exhibit resistance to neutralization in vitro.

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