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Biochemical, biophysical, and immunological characterization of respiratory secretions in severe SARS-CoV-2 infections.
Kratochvil, Michael J; Kaber, Gernot; Demirdjian, Sally; Cai, Pamela C; Burgener, Elizabeth B; Nagy, Nadine; Barlow, Graham L; Popescu, Medeea; Nicolls, Mark R; Ozawa, Michael G; Regula, Donald P; Pacheco-Navarro, Ana E; Yang, Samuel; de Jesus Perez, Vinicio A; Karmouty-Quintana, Harry; Peters, Andrew M; Zhao, Bihong; Buja, Maximilian L; Johnson, Pamela Y; Vernon, Robert B; Wight, Thomas N; Milla, Carlos E; Rogers, Angela J; Spakowitz, Andrew J; Heilshorn, Sarah C; Bollyky, Paul L.
Afiliação
  • Kratochvil MJ; Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Kaber G; Department of Materials Science and Engineering and.
  • Demirdjian S; Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Cai PC; Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Burgener EB; Department of Chemical Engineering, Stanford University, Stanford, California, USA.
  • Nagy N; Center for Excellence in Pulmonary Biology, Department of Pediatrics.
  • Barlow GL; Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Popescu M; Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Nicolls MR; Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Ozawa MG; Department of Pulmonology, Allergy and Critical Care Medicine.
  • Regula DP; Department of Pathology; and.
  • Pacheco-Navarro AE; Department of Pathology; and.
  • Yang S; Department of Pulmonology, Allergy and Critical Care Medicine.
  • de Jesus Perez VA; Department of Emergency Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Karmouty-Quintana H; Department of Pulmonology, Allergy and Critical Care Medicine.
  • Peters AM; Department of Biochemistry and Molecular Biology.
  • Zhao B; Divisions of Critical Care Medicine and Pulmonary and Sleep Medicine, Department of Internal Medicine.
  • Buja ML; Department of Biochemistry and Molecular Biology.
  • Johnson PY; Department of Pathology and Laboratory Medicine; and.
  • Vernon RB; Department of Internal Medicine, University of Texas Health Science Center - McGovern Medical School, Houston, Texas, USA.
  • Wight TN; Department of Pathology and Laboratory Medicine; and.
  • Milla CE; Matrix Biology Program, Benaroya Research Institute, Seattle, Washington, USA.
  • Rogers AJ; Matrix Biology Program, Benaroya Research Institute, Seattle, Washington, USA.
  • Spakowitz AJ; Matrix Biology Program, Benaroya Research Institute, Seattle, Washington, USA.
  • Bollyky PL; Center for Excellence in Pulmonary Biology, Department of Pediatrics.
JCI Insight ; 7(12)2022 06 22.
Article em En | MEDLINE | ID: mdl-35730564
ABSTRACT
Thick, viscous respiratory secretions are a major pathogenic feature of COVID-19, but the composition and physical properties of these secretions are poorly understood. We characterized the composition and rheological properties (i.e., resistance to flow) of respiratory secretions collected from intubated COVID-19 patients. We found the percentages of solids and protein content were greatly elevated in COVID-19 compared with heathy control samples and closely resembled levels seen in cystic fibrosis, a genetic disease known for thick, tenacious respiratory secretions. DNA and hyaluronan (HA) were major components of respiratory secretions in COVID-19 and were likewise abundant in cadaveric lung tissues from these patients. COVID-19 secretions exhibited heterogeneous rheological behaviors, with thicker samples showing increased sensitivity to DNase and hyaluronidase treatment. In histologic sections from these same patients, we observed increased accumulation of HA and the hyaladherin versican but reduced tumor necrosis factor-stimulated gene-6 staining, consistent with the inflammatory nature of these secretions. Finally, we observed diminished type I interferon and enhanced inflammatory cytokines in these secretions. Overall, our studies indicated that increases in HA and DNA in COVID-19 respiratory secretion samples correlated with enhanced inflammatory burden and suggested that DNA and HA may be viable therapeutic targets in COVID-19 infection.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Interferon Tipo I / COVID-19 Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Interferon Tipo I / COVID-19 Idioma: En Ano de publicação: 2022 Tipo de documento: Article