Nature Communications (Sep 2023)

Omicron variant neutralizing antibodies following BNT162b2 BA.4/5 versus mRNA-1273 BA.1 bivalent vaccination in patients with end-stage kidney disease

  • Kevin Yau,
  • Alexandra Kurtesi,
  • Freda Qi,
  • Melanie Delgado-Brand,
  • Tulunay R. Tursun,
  • Queenie Hu,
  • Miten Dhruve,
  • Christopher Kandel,
  • Omosomi Enilama,
  • Adeera Levin,
  • Yidi Jiang,
  • W. Rod Hardy,
  • Darren A. Yuen,
  • Jeffrey Perl,
  • Christopher T. Chan,
  • Jerome A. Leis,
  • Matthew J. Oliver,
  • Karen Colwill,
  • Anne-Claude Gingras,
  • Michelle A. Hladunewich

DOI
https://doi.org/10.1038/s41467-023-41678-9
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 8

Abstract

Read online

Abstract Neutralization of Omicron subvariants by different bivalent vaccines has not been well evaluated. This study characterizes neutralization against Omicron subvariants in 98 individuals on dialysis or with a kidney transplant receiving the BNT162b2 (BA.4/BA.5) or mRNA-1273 (BA.1) bivalent COVID-19 vaccine. Neutralization against Omicron BA.1, BA.5, BQ.1.1, and XBB.1.5 increased by 8-fold one month following bivalent vaccination. In comparison to wild-type (D614G), neutralizing antibodies against Omicron-specific variants were 7.3-fold lower against BA.1, 8.3-fold lower against BA.5, 45.8-fold lower against BQ.1.1, and 48.2-fold lower against XBB.1.5. Viral neutralization was not significantly different by bivalent vaccine type for wild-type (D614G) (P = 0.48), BA.1 (P = 0.21), BA.5 (P = 0.07), BQ.1.1 (P = 0.10), nor XBB.1.5 (P = 0.10). Hybrid immunity conferred higher neutralizing antibodies against all Omicron subvariants. This study provides evidence that BNT162b2 (BA.4/BA.5) and mRNA-1273 (BA.1) induce similar neutralization against Omicron subvariants, even when antigenically divergent from the circulating variant.