Endogenous antibody responses in REGN-COV2-treated SARS-CoV-2-infected individuals

Abstract Neutralizing monoclonal antibodies (mAbs) targeting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Spike glycoprotein have been developed for the treatment of COVID-19. Whilst antibody therapy has been shown to reduce the risk of COVID-19-associated hospitalization and death,...

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Published inOxford open immunology Vol. 4; no. 1; p. iqac012
Main Authors Kurshan, Ashwini, Snell, Luke B, Prior, Lucie, Tam, Jerry C H, Graham, Carl, Thangarajah, Rajeni, Edgeworth, Jonathan D, Nebbia, Gaia, Doores, Katie J
Format Journal Article
LanguageEnglish
Published England Oxford University Press 2023
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Summary:Abstract Neutralizing monoclonal antibodies (mAbs) targeting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Spike glycoprotein have been developed for the treatment of COVID-19. Whilst antibody therapy has been shown to reduce the risk of COVID-19-associated hospitalization and death, there is limited understanding of the endogenous immunity to SARS-CoV-2 generated in mAb-treated patients and therefore ongoing susceptibility to future infections. Here we measure the endogenous antibody response in SARS-CoV-2-infected individuals treated with REGN-COV2 (Ronapreve). We show that in the majority of unvaccinated, delta-infected REGN-COV2-treated individuals, an endogenous antibody response is generated, but, like untreated, delta-infected individuals, there was a limited neutralization breadth. However, some vaccinated individuals who were seronegative at SARS-CoV-2 infection baseline and some unvaccinated individuals failed to produce an endogenous immune response following infection and REGN-COV2 treatment demonstrating the importance of mAb therapy in some patient populations.
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ISSN:2633-6960
2633-6960
DOI:10.1093/oxfimm/iqac012