4.8 Article

Antibody escape of SARS-CoV-2 Omicron BA.4 and BA.5 from vaccine and BA.1 serum

Journal

CELL
Volume 185, Issue 14, Pages 2422-+

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2022.06.005

Keywords

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Funding

  1. Chinese Academy of Medical Sciences (CAMS) Innovation Fund for Medical Science (CIFMS), China [2018-I2M-2-002]
  2. Schmidt Futures
  3. Red Avenue Foundation
  4. Oak Foundation
  5. Wellcome [101122/Z/13/Z, 090532/Z/09/Z, 203141/Z/16/Z]
  6. UKRI MRC [MR/N00065X/1]
  7. Medical Research Council [MC_PC_19059]
  8. NIHR Oxford BRC
  9. UK Research and Innovation
  10. Coalition for Epidemic Preparedness Innovations
  11. National Institute for Health Research (NIHR)
  12. NIHR Oxford Biomedical Research Centre
  13. Thames Valley and South Midland's NIHR Clinical Research Network
  14. UK Department of Health and Social Care
  15. UK Coronavirus Immunology Consortium (UK-CIC)
  16. Huo Family Foundation
  17. NIH [WT109965MA, U19 I082360]
  18. NIHR Global Research Professorship [NIHR300791]
  19. Wellcome Trust [101122/Z/13/Z] Funding Source: Wellcome Trust

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The Omicron variant of SARS-CoV-2 has rapidly spread globally and has evolved into different sublineages, with BA.4 and BA.5 dominating in South Africa. These sublineages show reduced neutralization by vaccine and naturally immune serum, indicating the possibility of repeat Omicron infections.
The Omicron lineage of SARS-CoV-2, which was first described in November 2021, spread rapidly to become globally dominant and has split into a number of sublineages. BA.1 dominated the initial wave but has been replaced by BA.2 in many countries. Recent sequencing from South Africa???s Gauteng region uncovered two new sublineages, BA.4 and BA.5, which are taking over locally, driving a new wave. BA.4 and BA.5 contain identical spike sequences, and although closely related to BA.2, they contain further mutations in the recep-tor-binding domain of their spikes. Here, we study the neutralization of BA.4/5 using a range of vaccine and naturally immune serum and panels of monoclonal antibodies. BA.4/5 shows reduced neutralization by the serum from individuals vaccinated with triple doses of AstraZeneca or Pfizer vaccine compared with BA.1 and BA.2. Furthermore, using the serum from BA.1 vaccine breakthrough infections, there are, likewise, sig-nificant reductions in the neutralization of BA.4/5, raising the possibility of repeat Omicron infections.

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