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Intranasal administration of convalescent plasma protects against SARS-CoV-2 infection in hamsters

BACKGROUND: Convalescent plasma (CP) transfusion is an early option for treating infections with pandemic potential, often preceding vaccine or antiviral drug rollout. Heterogenous findings from randomized clinical trials on transfusion of COVID-19 CP (CCP) have been reported. However, meta-analysis...

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Autores principales: Wouters, Elise, Verbrugghe, Caro, Abdelnabi, Rana, Devloo, Rosalie, De Clippel, Dorien, Jochmans, Dirk, De Bleser, Dominique, Weynand, Birgit, Compernolle, Veerle, Neyts, Johan, Feys, Hendrik B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171892/
https://www.ncbi.nlm.nih.gov/pubmed/37148586
http://dx.doi.org/10.1016/j.ebiom.2023.104597
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author Wouters, Elise
Verbrugghe, Caro
Abdelnabi, Rana
Devloo, Rosalie
De Clippel, Dorien
Jochmans, Dirk
De Bleser, Dominique
Weynand, Birgit
Compernolle, Veerle
Neyts, Johan
Feys, Hendrik B.
author_facet Wouters, Elise
Verbrugghe, Caro
Abdelnabi, Rana
Devloo, Rosalie
De Clippel, Dorien
Jochmans, Dirk
De Bleser, Dominique
Weynand, Birgit
Compernolle, Veerle
Neyts, Johan
Feys, Hendrik B.
author_sort Wouters, Elise
collection PubMed
description BACKGROUND: Convalescent plasma (CP) transfusion is an early option for treating infections with pandemic potential, often preceding vaccine or antiviral drug rollout. Heterogenous findings from randomized clinical trials on transfusion of COVID-19 CP (CCP) have been reported. However, meta-analysis suggests that transfusion of high titer CCP is associated with a mortality benefit for COVID-19 outpatients or inpatients treated within 5 days after symptom onset, indicating the importance of early administration. METHODS: We tested if CCP is an effective prophylactic against SARS-CoV-2 infection by the intranasal administration of 25 μL CCP/nostril (i.e. 0.01–0.06 mg anti-RBD antibodies/kg) in hamsters exposed to infected littermates. FINDINGS: In this model, 40% of CCP treated hamsters were fully protected and 40% had significantly reduced viral loads, the remaining 20% was not protected. The effect seems dose-dependent because high-titer CCP from a vaccinated donor was more effective than low-titer CCP from a donation prior to vaccine rollout. Intranasal administration of human CCP resulted in a reactive (immune) response in hamster lungs, however this was not observed upon administration of hamster CCP. INTERPRETATION: We conclude that CCP is an effective prophylactic when used directly at the site of primary infection. This option should be considered in future prepandemic preparedness plans. FUNDING: 10.13039/100012331Flanders Innovation & Entrepreneurship (VLAIO) and the Foundation for Scientific Research of the Belgian Red Cross Flanders.
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spelling pubmed-101718922023-05-11 Intranasal administration of convalescent plasma protects against SARS-CoV-2 infection in hamsters Wouters, Elise Verbrugghe, Caro Abdelnabi, Rana Devloo, Rosalie De Clippel, Dorien Jochmans, Dirk De Bleser, Dominique Weynand, Birgit Compernolle, Veerle Neyts, Johan Feys, Hendrik B. eBioMedicine Articles BACKGROUND: Convalescent plasma (CP) transfusion is an early option for treating infections with pandemic potential, often preceding vaccine or antiviral drug rollout. Heterogenous findings from randomized clinical trials on transfusion of COVID-19 CP (CCP) have been reported. However, meta-analysis suggests that transfusion of high titer CCP is associated with a mortality benefit for COVID-19 outpatients or inpatients treated within 5 days after symptom onset, indicating the importance of early administration. METHODS: We tested if CCP is an effective prophylactic against SARS-CoV-2 infection by the intranasal administration of 25 μL CCP/nostril (i.e. 0.01–0.06 mg anti-RBD antibodies/kg) in hamsters exposed to infected littermates. FINDINGS: In this model, 40% of CCP treated hamsters were fully protected and 40% had significantly reduced viral loads, the remaining 20% was not protected. The effect seems dose-dependent because high-titer CCP from a vaccinated donor was more effective than low-titer CCP from a donation prior to vaccine rollout. Intranasal administration of human CCP resulted in a reactive (immune) response in hamster lungs, however this was not observed upon administration of hamster CCP. INTERPRETATION: We conclude that CCP is an effective prophylactic when used directly at the site of primary infection. This option should be considered in future prepandemic preparedness plans. FUNDING: 10.13039/100012331Flanders Innovation & Entrepreneurship (VLAIO) and the Foundation for Scientific Research of the Belgian Red Cross Flanders. Elsevier 2023-05-04 /pmc/articles/PMC10171892/ /pubmed/37148586 http://dx.doi.org/10.1016/j.ebiom.2023.104597 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles
Wouters, Elise
Verbrugghe, Caro
Abdelnabi, Rana
Devloo, Rosalie
De Clippel, Dorien
Jochmans, Dirk
De Bleser, Dominique
Weynand, Birgit
Compernolle, Veerle
Neyts, Johan
Feys, Hendrik B.
Intranasal administration of convalescent plasma protects against SARS-CoV-2 infection in hamsters
title Intranasal administration of convalescent plasma protects against SARS-CoV-2 infection in hamsters
title_full Intranasal administration of convalescent plasma protects against SARS-CoV-2 infection in hamsters
title_fullStr Intranasal administration of convalescent plasma protects against SARS-CoV-2 infection in hamsters
title_full_unstemmed Intranasal administration of convalescent plasma protects against SARS-CoV-2 infection in hamsters
title_short Intranasal administration of convalescent plasma protects against SARS-CoV-2 infection in hamsters
title_sort intranasal administration of convalescent plasma protects against sars-cov-2 infection in hamsters
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171892/
https://www.ncbi.nlm.nih.gov/pubmed/37148586
http://dx.doi.org/10.1016/j.ebiom.2023.104597
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