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Nebulized mRNA-Encoded Antibodies Protect Hamsters from SARS-CoV-2 Infection.
Vanover, Daryll; Zurla, Chiara; Peck, Hannah E; Orr-Burks, Nichole; Joo, Jae Yeon; Murray, Jackelyn; Holladay, Nathan; Hobbs, Ryan A; Jung, Younghun; Chaves, Lorena C S; Rotolo, Laura; Lifland, Aaron W; Olivier, Alicia K; Li, Dapeng; Saunders, Kevin O; Sempowski, Gregory D; Crowe, James E; Haynes, Barton F; Lafontaine, Eric R; Hogan, Robert J; Santangelo, Philip J.
  • Vanover D; Wallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, 30322, USA.
  • Zurla C; Wallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, 30322, USA.
  • Peck HE; Wallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, 30322, USA.
  • Orr-Burks N; Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, Athens, GA, 30602, USA.
  • Joo JY; Wallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, 30322, USA.
  • Murray J; Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, Athens, GA, 30602, USA.
  • Holladay N; Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, Athens, GA, 30602, USA.
  • Hobbs RA; Wallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, 30322, USA.
  • Jung Y; Wallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, 30322, USA.
  • Chaves LCS; Wallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, 30322, USA.
  • Rotolo L; Wallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, 30322, USA.
  • Lifland AW; Wallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, 30322, USA.
  • Olivier AK; Department of Pathobiology and Population Medicine, College of Veterinary Medicine, Mississippi State University, Starkville, MS, 39762, USA.
  • Li D; Duke Human Vaccine Institute and the Departments of Medicine and Immunology, Duke University School of Medicine, Durham, NC, 27710, USA.
  • Saunders KO; Duke Human Vaccine Institute, Departments of Surgery, Molecular Genetics and Microbiology, and Immunology, Duke University School of Medicine, Durham, NC, 27710, USA.
  • Sempowski GD; Duke Human Vaccine Institute and the Departments of Medicine and Immunology, Duke University School of Medicine, Durham, NC, 27710, USA.
  • Crowe JE; Vanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
  • Haynes BF; Duke Human Vaccine Institute and the Departments of Medicine and Immunology, Duke University School of Medicine, Durham, NC, 27710, USA.
  • Lafontaine ER; Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, Athens, GA, 30602, USA.
  • Hogan RJ; Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, Athens, GA, 30602, USA.
  • Santangelo PJ; Department of Veterinary Biosciences and Diagnostic Imaging, College of Veterinary Medicine, University of Georgia, Athens, GA, 30602, USA.
Adv Sci (Weinh) ; : e2202771, 2022 Oct 31.
Article in English | MEDLINE | ID: covidwho-2094138
ABSTRACT
Despite the success of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2vaccines, there remains a clear need for new classes of preventatives for respiratory viral infections due to vaccine hesitancy, lack of sterilizing immunity, and for at-risk patient populations, including the immunocompromised. While many neutralizing antibodies have been identified, and several approved, to treat COVID-19, systemic delivery, large doses, and high costs have the potential to limit their widespread use, especially in low- and middle-income countries. To use these antibodies more efficiently, an inhalable formulation is developed that allows for the expression of mRNA-encoded, membrane-anchored neutralizing antibodies in the lung to mitigate SARS-CoV-2 infections. First, the ability of mRNA-encoded, membrane-anchored, anti-SARS-CoV-2 antibodies to prevent infections in vitro is demonstrated. Next, it is demonstrated that nebulizer-based delivery of these mRNA-expressed neutralizing antibodies potently abrogates disease in the hamster model. Overall, these results support the use of nebulizer-based mRNA expression of neutralizing antibodies as a new paradigm for mitigating respiratory virus infections.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Prognostic study Topics: Vaccines Language: English Journal: Adv Sci (Weinh) Year: 2022 Document Type: Article Affiliation country: Advs.202202771

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Prognostic study Topics: Vaccines Language: English Journal: Adv Sci (Weinh) Year: 2022 Document Type: Article Affiliation country: Advs.202202771