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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. / Guselnikov, Sergey V.; Baranov, Konstantin O.; Kulemzin, Sergey V. et al.

In: Frontiers in Immunology, Vol. 15, 1442160, 09.08.2024.

Research output: Contribution to journalArticlepeer-review

Harvard

Guselnikov, SV, Baranov, KO, Kulemzin, SV, Belovezhets, TN, Chikaev, AN, Murasheva, SV, Volkova, OY, Mechetina, LV, Najakshin, AM, Chikaev, NA, Solodkov, PP, Sergeeva, MV, Smirnov, AV, Serova, IA, Serov, OL, Markhaev, AG, Kononova, YV, Alekseev, AY, Gulyaeva, MA, Danilenko, DM, Battulin, NR, Shestopalov, AM & Taranin, AV 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', Frontiers in Immunology, vol. 15, 1442160. https://doi.org/10.3389/fimmu.2024.1442160

APA

Guselnikov, S. V., Baranov, K. O., Kulemzin, S. V., Belovezhets, T. N., Chikaev, A. N., Murasheva, S. V., Volkova, O. Y., Mechetina, L. V., Najakshin, A. M., Chikaev, N. A., Solodkov, P. P., Sergeeva, M. V., Smirnov, A. V., Serova, I. A., Serov, O. L., Markhaev, A. G., Kononova, Y. V., Alekseev, A. Y., Gulyaeva, M. A., ... Taranin, A. V. (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. Frontiers in Immunology, 15, [1442160]. https://doi.org/10.3389/fimmu.2024.1442160

Vancouver

Guselnikov SV, Baranov KO, Kulemzin SV, Belovezhets TN, Chikaev AN, Murasheva SV et al. 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. Frontiers in Immunology. 2024 Aug 9;15:1442160. doi: 10.3389/fimmu.2024.1442160

Author

BibTeX

@article{80a5f2a8919741a689631de9fc1fbd02,
title = "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",
abstract = "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.",
keywords = "COVID-19, Omicron, SARS-CoV-1, iC1 antibody, in vivo protection",
author = "Guselnikov, {Sergey V.} and Baranov, {Konstantin O.} and Kulemzin, {Sergey V.} and Belovezhets, {Tatyana N.} and Chikaev, {Anton N.} and Murasheva, {Svetlana V.} and Volkova, {Olga Y.} and Mechetina, {Ludmila V.} and Najakshin, {Alexander M.} and Chikaev, {Nikolai A.} and Solodkov, {Pavel P.} and Sergeeva, {Maria V.} and Smirnov, {Alexander V.} and Serova, {Irina A.} and Serov, {Oleg L.} and Markhaev, {Alexander G.} and Kononova, {Yulia V.} and Alekseev, {Alexander Y.} and Gulyaeva, {Marina A.} and Danilenko, {Daria M.} and Battulin, {Nariman R.} and Shestopalov, {Alexander M.} and Taranin, {Alexander V.}",
note = "The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This research was funded by the Ministry of Science and Higher Education of the Russian Federation (Agreement No 075-15-2021-1086, contract No RF—193021X0015, 15.ИП.21.0015).",
year = "2024",
month = aug,
day = "9",
doi = "10.3389/fimmu.2024.1442160",
language = "English",
volume = "15",
journal = "Frontiers in Immunology",
issn = "1664-3224",
publisher = "Frontiers Media S.A.",

}

RIS

TY - JOUR

T1 - 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

AU - Guselnikov, Sergey V.

AU - Baranov, Konstantin O.

AU - Kulemzin, Sergey V.

AU - Belovezhets, Tatyana N.

AU - Chikaev, Anton N.

AU - Murasheva, Svetlana V.

AU - Volkova, Olga Y.

AU - Mechetina, Ludmila V.

AU - Najakshin, Alexander M.

AU - Chikaev, Nikolai A.

AU - Solodkov, Pavel P.

AU - Sergeeva, Maria V.

AU - Smirnov, Alexander V.

AU - Serova, Irina A.

AU - Serov, Oleg L.

AU - Markhaev, Alexander G.

AU - Kononova, Yulia V.

AU - Alekseev, Alexander Y.

AU - Gulyaeva, Marina A.

AU - Danilenko, Daria M.

AU - Battulin, Nariman R.

AU - Shestopalov, Alexander M.

AU - Taranin, Alexander V.

N1 - The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This research was funded by the Ministry of Science and Higher Education of the Russian Federation (Agreement No 075-15-2021-1086, contract No RF—193021X0015, 15.ИП.21.0015).

PY - 2024/8/9

Y1 - 2024/8/9

N2 - 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.

AB - 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.

KW - COVID-19

KW - Omicron

KW - SARS-CoV-1

KW - iC1 antibody

KW - in vivo protection

UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85200381438&origin=inward&txGid=1b25149c8896911748bf44141650a01d

UR - https://www.webofscience.com/wos/woscc/full-record/WOS:001282648900001

UR - https://www.mendeley.com/catalogue/335b71fa-da14-3156-ac71-406c6ac247e4/

U2 - 10.3389/fimmu.2024.1442160

DO - 10.3389/fimmu.2024.1442160

M3 - Article

C2 - 39100673

VL - 15

JO - Frontiers in Immunology

JF - Frontiers in Immunology

SN - 1664-3224

M1 - 1442160

ER -

ID: 61205436