Omicron extensively but incompletely escapes Pfizer BNT162b2 neutralization

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  • Sandile Cele
  • Laurelle Jackson
  • David S. Khoury
  • Khadija Khan
  • Thandeka Moyo-Gwete
  • Houriiyah Tegally
  • James Emmanuel San
  • Deborah Cromer
  • Cathrine Scheepers
  • Daniel G. Amoako
  • Farina Karim
  • Mallory Bernstein
  • Gila Lustig
  • Derseree Archary
  • Muneerah Smith
  • Yashica Ganga
  • Zesuliwe Jule
  • Kajal Reedoy
  • Shi Hsia Hwa
  • Jennifer Giandhari
  • Jonathan M. Blackburn
  • Bernadett I. Gosnell
  • Salim S. Abdool Karim
  • Willem Hanekom
  • Mary Ann Davies
  • Marvin Hsiao
  • Darren Martin
  • Koleka Mlisana
  • Constantinos Kurt Wibmer
  • Carolyn Williamson
  • Denis York
  • Rohen Harrichandparsad
  • Kobus Herbst
  • Prakash Jeena
  • Thandeka Khoza
  • Kløverpris, Henrik Nyhus
  • Alasdair Leslie
  • Rajhmun Madansein
  • Nombulelo Magula
  • Nithendra Manickchund
  • Mohlopheni Marakalala
  • Matilda Mazibuko
  • Mosa Moshabela
  • Ntombifuthi Mthabela
  • Kogie Naidoo
  • Zaza Ndhlovu
  • Thumbi Ndung’u
  • Nokuthula Ngcobo
  • Kennedy Nyamande
  • Vinod Patel
  • NGS-SA
  • COMMIT-KZN Team

The emergence of the SARS-CoV-2 variant of concern Omicron (Pango lineage B.1.1.529), first identified in Botswana and South Africa, may compromise vaccine effectiveness and lead to re-infections1. Here we investigated Omicron escape from neutralization by antibodies from South African individuals vaccinated with Pfizer BNT162b2. We used blood samples taken soon after vaccination from individuals who were vaccinated and previously infected with SARS-CoV-2 or vaccinated with no evidence of previous infection. We isolated and sequence-confirmed live Omicron virus from an infected person and observed that Omicron requires the angiotensin-converting enzyme 2 (ACE2) receptor to infect cells. We compared plasma neutralization of Omicron relative to an ancestral SARS-CoV-2 strain and found that neutralization of ancestral virus was much higher in infected and vaccinated individuals compared with the vaccinated-only participants. However, both groups showed a 22-fold reduction in vaccine-elicited neutralization by the Omicron variant. Participants who were vaccinated and had previously been infected exhibited residual neutralization of Omicron similar to the level of neutralization of the ancestral virus observed in the vaccination-only group. These data support the notion that reasonable protection against Omicron may be maintained using vaccination approaches.

OriginalsprogEngelsk
TidsskriftNature
Vol/bind602
Udgave nummer7898
Sider (fra-til)654-656
Antal sider3
ISSN0028-0836
DOI
StatusUdgivet - 2022

Bibliografisk note

Funding Information:
Acknowledgements This study was supported by the Bill and Melinda Gates award INV-018944 (A.S.), National Institutes of Health award R01 AI138546 (A.S.), and South African Medical Research Council awards (A.S., T.d.O. and P.L.M.) and the UK Foreign, Commonwealth and Development Office and Wellcome Trust (grant no. 221003/Z/20/Z to P.L.M.). P.L.M. is also supported by the South African Research Chairs Initiative of the Department of Science and Innovation and the NRF (grant no. 98341). D.S.K., D.C. and M.P.D. are supported by NHMRC (Australia) Fellowship/Investigator grants. D.A. was supported by the European and Developing Countries Clinical Trials Partnership (EDCTP) Senior Fellowship (grant no. TMA2017SF-1960). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Publisher Copyright:
© 2021, The Author(s).

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