Administration of vaccine-boosted COVID-19 convalescent plasma to SARS-CoV-2 infected hamsters decreases virus replication in lungs and hastens resolution of the infection despite transiently enhancing disease and lung pathology.

COVID-19 animal models immune plasma transfusion

Journal

bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187

Informations de publication

Date de publication:
23 Aug 2023
Historique:
pubmed: 4 9 2023
medline: 4 9 2023
entrez: 4 9 2023
Statut: epublish

Résumé

The utility of COVID-19 convalescent plasma (CCP) for treatment of immunocompromised patients who are not able to mount a protective antibody response against SARS-CoV-2 and who have contraindications or adverse effects from currently available antivirals remains unclear. To better understand the mechanism of protection in CCP, we studied viral replication and disease progression in SARS-CoV-2 infected hamsters treated with CCP plasma obtained from recovered COVID patients that had also been vaccinated with an mRNA vaccine, hereafter referred to as Vaxplas. We found that Vaxplas dramatically reduced virus replication in the lungs and improved infection outcome in SARS-CoV-2 infected hamsters. However, we also found that Vaxplas transiently enhanced disease severity and lung pathology in treated animals likely due to the deposition of immune complexes, activation of complement and recruitment of increased numbers of macrophages with an M1 proinflammatory phenotype into the lung parenchyma.

Identifiants

pubmed: 37662344
doi: 10.1101/2023.08.22.553458
pmc: PMC10473650
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI118590
Pays : United States

Auteurs

Timothy D Carroll (TD)

Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California Davis, Davis, California, USA.
California National Primate Research Center, University of California Davis, Davis, California, USA.

Talia Wong (T)

Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California Davis, Davis, California, USA.

Mary Kate Morris (MK)

Division of Viral and Rickettsial Diseases, California Department of Public Health, Richmond, California, USA.

Clara Di Germanio (C)

Vitalant Research Institute, San Francisco, CA, USA.

Zhong-Min Ma (ZM)

California National Primate Research Center, University of California Davis, Davis, California, USA.

Mars Stone (M)

Vitalant Research Institute, San Francisco, CA, USA.

Erin Ball (E)

Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California Davis, Davis, California, USA.

Linda Fritts (L)

Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California Davis, Davis, California, USA.
California National Primate Research Center, University of California Davis, Davis, California, USA.

Arjun Rustagi (A)

Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Palo Alto, California, USA.

Graham Simmons (G)

Vitalant Research Institute, San Francisco, CA, USA.

Michael Busch (M)

Vitalant Research Institute, San Francisco, CA, USA.

Christopher J Miller (CJ)

Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California Davis, Davis, California, USA.
California National Primate Research Center, University of California Davis, Davis, California, USA.
Division of Infectious Diseases, Department of Internal Medicine, School of Medicine, University of California Davis, Sacramento, California, USA.

Classifications MeSH