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Oxford University Press - PMC COVID-19 Collection logoLink to Oxford University Press - PMC COVID-19 Collection
. 2021 May 27:jiab289. doi: 10.1093/infdis/jiab289

SARS-CoV-2 neutralizing human antibodies protect against lower respiratory tract disease in a hamster model

Bart L Haagmans 1,#, Danny Noack 1, Nisreen M A Okba 1, Wentao Li 5, Chunyan Wang 5, Theo Bestebroer 1, Rory de Vries 1, Sander Herfst 1, Dennis de Meulder 1, Elwin Verveer 1, Peter van Run 1, Mart M Lamers 1, Bart Rijnders 2, Casper Rokx 2, Frank van Kuppeveld 5, Frank Grosveld 3,4, Dubravka Drabek 3,4, Corine GeurtsvanKessel 1, Marion Koopmans 1, Berend Jan Bosch 5, Thijs Kuiken 1, Barry Rockx 1,#,
PMCID: PMC8243397  PMID: 34043806

Abstract

Effective clinical intervention strategies for COVID-19 are urgently needed. Although several clinical trials have evaluated the use of convalescent plasma containing virus-neutralizing antibodies, the levels of neutralizing antibodies are usually not assessed and the effectiveness has not been proven. We show that hamsters treated prophylactically with a 1:2560 titer of human convalescent plasma or a 1:5260 titer of monoclonal antibody were protected against weight loss, had a significant reduction of virus replication in the lungs and showed reduced pneumonia . Interestingly, this protective effect was lost with a titer of 1:320 of convalescent plasma. These data highlight the importance of screening plasma donors for high levels of neutralizing antibodies.

Our data show that prophylactic administration of high levels of neutralizing antibody, either monoclonal or from convalescent plasma, prevent severe SARS-CoV-2 pneumonia in a hamster model, and could be used as an alternative or complementary to other antiviral treatments for COVID-19.

Keywords: SARS-CoV-2, convalescent plasma, monoclonal antibody, hamster, pneumonia

Supplementary Material

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jiab289_suppl_Supplementary_Materials
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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

jiab289_suppl_Supplementary_Figure_S1
jiab289_suppl_Supplementary_Figure_S2
jiab289_suppl_Supplementary_Materials
jiab289_suppl_Supplementary_Table_S1
jiab289_suppl_Supplementary_Table_S2

Articles from The Journal of Infectious Diseases are provided here courtesy of Oxford University Press

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