Cell Reports (May 2022)

ChAdOx1 nCoV-19 vaccine elicits monoclonal antibodies with cross-neutralizing activity against SARS-CoV-2 viral variants

  • Jeffrey Seow,
  • Carl Graham,
  • Sadie R. Hallett,
  • Thomas Lechmere,
  • Thomas J.A. Maguire,
  • Isabella Huettner,
  • Daniel Cox,
  • Hataf Khan,
  • Suzanne Pickering,
  • Rebekah Roberts,
  • Anele Waters,
  • Christopher C. Ward,
  • Christine Mant,
  • Michael J. Pitcher,
  • Jo Spencer,
  • Julie Fox,
  • Michael H. Malim,
  • Katie J. Doores

Journal volume & issue
Vol. 39, no. 5
p. 110757

Abstract

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Summary: Although the antibody response to COVID-19 vaccination has been studied extensively at the polyclonal level using immune sera, little has been reported on the antibody response at the monoclonal level. Here, we isolate a panel of 44 anti-SARS-CoV-2 monoclonal antibodies (mAbs) from an individual who received two doses of the ChAdOx1 nCoV-19 (AZD1222) vaccine at a 12-week interval. We show that, despite a relatively low serum neutralization titer, Spike-reactive IgG+ B cells are still detectable 9 months post-boost. Furthermore, mAbs with potent neutralizing activity against the current SARS-CoV-2 variants of concern (Alpha, Gamma, Beta, Delta, and Omicron) are present. The vaccine-elicited neutralizing mAbs form eight distinct competition groups and bind epitopes overlapping with neutralizing mAbs elicited following SARS-CoV-2 infection. AZD1222-elicited mAbs are more mutated than mAbs isolated from convalescent donors 1–2 months post-infection. These findings provide molecular insights into the AZD1222 vaccine-elicited antibody response.

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