npj Vaccines (Apr 2022)

BNT162b2-elicited neutralization of Delta plus, Lambda, Mu, B.1.1.519, and Theta SARS-CoV-2 variants

  • Jianying Liu,
  • Yang Liu,
  • Hongjie Xia,
  • Jing Zou,
  • Scott C. Weaver,
  • Kena A. Swanson,
  • Hui Cai,
  • Mark Cutler,
  • David Cooper,
  • Alexander Muik,
  • Kathrin U. Jansen,
  • Ugur Sahin,
  • Xuping Xie,
  • Philip R. Dormitzer,
  • Pei-Yong Shi

DOI
https://doi.org/10.1038/s41541-022-00462-4
Journal volume & issue
Vol. 7, no. 1
pp. 1 – 4

Abstract

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Abstract BNT162b2-elicited human sera neutralize the currently dominant Delta SARS-CoV-2 variant. Here, we report the ability of 20 human sera, drawn 2 or 4 weeks after two doses of BNT162b2, to neutralize USA-WA1/2020 SARS-CoV-2 bearing variant spikes from Delta plus (Delta-AY.1, Delta-AY.2), Delta-∆144 (Delta with the Y144 deletion of the Alpha variant), Lambda, B.1.1.519, Theta, and Mu lineage viruses. Geometric mean plaque reduction neutralization titers against Delta-AY.1, Delta-AY.2, and Mu viruses are slightly lower than against USA-WA1/2020, but all sera neutralize the variant viruses to titers of ≥80, and neutralization titers against the Delta-∆144, Lambda, B.1.1.519 and Theta variants not significantly reduced relative to those against USA-WA1/2020. The susceptibility of Delta plus, Lambda, B.1.1.519, Theta, Mu, and other variants to neutralization by the sera indicates that antigenic change has not led to virus escape from vaccine-elicited neutralizing antibodies and supports ongoing mass immunization with BNT162b2 to control the variants and to minimize the emergence of new variants.