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Development of an In Vivo Probe to Track SARS-CoV-2 Infection in Rhesus Macaques.
Madden, Patrick J; Arif, Muhammad S; Becker, Mark E; McRaven, Michael D; Carias, Ann M; Lorenzo-Redondo, Ramon; Xiao, Sixia; Midkiff, Cecily C; Blair, Robert V; Potter, Elizabeth Lake; Martin-Sancho, Laura; Dodson, Alan; Martinelli, Elena; Todd, John-Paul M; Villinger, Francois J; Chanda, Sumit K; Aye, Pyone Pyone; Roy, Chad J; Roederer, Mario; Lewis, Mark G; Veazey, Ronald S; Hope, Thomas J.
Afiliação
  • Madden PJ; Department of Cell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.
  • Arif MS; Department of Cell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.
  • Becker ME; Department of Cell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.
  • McRaven MD; Department of Cell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.
  • Carias AM; Department of Cell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.
  • Lorenzo-Redondo R; Department of Medicine, Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.
  • Xiao S; Center for Pathogen Genomics and Microbial Evolution, Northwestern University Institute for Global Health, Chicago, IL, United States.
  • Midkiff CC; Department of Cell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.
  • Blair RV; Division of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, United States.
  • Potter EL; Division of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, United States.
  • Martin-Sancho L; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.
  • Dodson A; Immunity and Pathogenesis Program, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, United States.
  • Martinelli E; Bioqual Inc., Rockville, MD, United States.
  • Todd JM; Department of Cell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.
  • Villinger FJ; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.
  • Chanda SK; New Iberia Research Center, University of Louisiana-Lafayette, New Iberia, LA, United States.
  • Aye PP; Immunity and Pathogenesis Program, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, United States.
  • Roy CJ; Division of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, United States.
  • Roederer M; Division of Microbiology, Tulane National Primate Research Center, Covington, LA, United States.
  • Lewis MG; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.
  • Veazey RS; Bioqual Inc., Rockville, MD, United States.
  • Hope TJ; Division of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, United States.
Front Immunol ; 12: 810047, 2021.
Article em En | MEDLINE | ID: mdl-35003140
ABSTRACT
Infection with the novel coronavirus, SARS-CoV-2, results in pneumonia and other respiratory symptoms as well as pathologies at diverse anatomical sites. An outstanding question is whether these diverse pathologies are due to replication of the virus in these anatomical compartments and how and when the virus reaches those sites. To answer these outstanding questions and study the spatiotemporal dynamics of SARS-CoV-2 infection a method for tracking viral spread in vivo is needed. We developed a novel, fluorescently labeled, antibody-based in vivo probe system using the anti-spike monoclonal antibody CR3022 and demonstrated that it could successfully identify sites of SARS-CoV-2 infection in a rhesus macaque model of COVID-19. Our results showed that the fluorescent signal from our antibody-based probe could differentiate whole lungs of macaques infected for 9 days from those infected for 2 or 3 days. Additionally, the probe signal corroborated the frequency and density of infected cells in individual tissue blocks from infected macaques. These results provide proof of concept for the use of in vivo antibody-based probes to study SARS-CoV-2 infection dynamics in rhesus macaques.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Replicação Viral / Imunofluorescência / Anticorpos Neutralizantes / SARS-CoV-2 / Anticorpos Monoclonais / Anticorpos Antivirais Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Replicação Viral / Imunofluorescência / Anticorpos Neutralizantes / SARS-CoV-2 / Anticorpos Monoclonais / Anticorpos Antivirais Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article