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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.
Carroll, Timothy D; Wong, Talia; Morris, Mary Kate; Di Germanio, Clara; Ma, Zhong-Min; Stone, Mars; Ball, Erin; Fritts, Linda; Rustagi, Arjun; Simmons, Graham; Busch, Michael; Miller, Christopher J.
Afiliação
  • Carroll TD; Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California Davis, Davis, California, USA.
  • Wong T; California National Primate Research Center, University of California Davis, Davis, California, USA.
  • Morris MK; Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California Davis, Davis, California, USA.
  • Di Germanio C; Division of Viral and Rickettsial Diseases, California Department of Public Health, Richmond, California, USA.
  • Ma ZM; Vitalant Research Institute, San Francisco, CA, USA.
  • Stone M; California National Primate Research Center, University of California Davis, Davis, California, USA.
  • Ball E; Vitalant Research Institute, San Francisco, CA, USA.
  • Fritts L; Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California Davis, Davis, California, USA.
  • Rustagi A; Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California Davis, Davis, California, USA.
  • Simmons G; California National Primate Research Center, University of California Davis, Davis, California, USA.
  • Busch M; Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Palo Alto, California, USA.
  • Miller CJ; Vitalant Research Institute, San Francisco, CA, USA.
bioRxiv ; 2023 Aug 23.
Article em En | MEDLINE | ID: mdl-37662344
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos