Frontiers in Immunology (Jul 2024)

A potent, broadly neutralizing human monoclonal antibody that efficiently protects hACE2-transgenic mice from infection with the Wuhan, BA.5, and XBB.1.5 SARS-CoV-2 variants

  • Sergey V. Guselnikov,
  • Konstantin O. Baranov,
  • Sergey V. Kulemzin,
  • Tatyana N. Belovezhets,
  • Anton N. Chikaev,
  • Svetlana V. Murasheva,
  • Olga Y. Volkova,
  • Ludmila V. Mechetina,
  • Alexander M. Najakshin,
  • Nikolai A. Chikaev,
  • Pavel P. Solodkov,
  • Maria V. Sergeeva,
  • Alexander V. Smirnov,
  • Irina A. Serova,
  • Oleg L. Serov,
  • Alexander G. Markhaev,
  • Yulia V. Kononova,
  • Alexander Y. Alekseev,
  • Alexander Y. Alekseev,
  • Marina A. Gulyaeva,
  • Marina A. Gulyaeva,
  • Daria M. Danilenko,
  • Nariman R. Battulin,
  • Nariman R. Battulin,
  • Alexander M. Shestopalov,
  • Alexander M. Shestopalov,
  • Alexander V. Taranin

DOI
https://doi.org/10.3389/fimmu.2024.1442160
Journal volume & issue
Vol. 15

Abstract

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The COVID-19 pandemic has uncovered the high genetic variability of the SARS-CoV-2 virus and its ability to evade the immune responses that were induced by earlier viral variants. Only a few monoclonal antibodies that have been reported to date are capable of neutralizing a broad spectrum of SARS-CoV-2 variants. Here, we report the isolation of a new broadly neutralizing human monoclonal antibody, iC1. The antibody was identified through sorting the SARS-CoV-1 RBD-stained individual B cells that were isolated from the blood of a vaccinated donor following a breakthrough infection. In vitro, iC1 potently neutralizes pseudoviruses expressing a wide range of SARS-CoV-2 Spike variants, including those of the XBB sublineage. In an hACE2-transgenic mouse model, iC1 provided effective protection against the Wuhan strain of the virus as well as the BA.5 and XBB.1.5 variants. Therefore, iC1 can be considered as a potential component of the broadly neutralizing antibody cocktails resisting the SARS-CoV-2 mutation escape.

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