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Biochemical, Biophysical, and Immunological Characterization of Respiratory Secretions in Severe SARS-CoV-2 (COVID-19) 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, Stanford University, Stanford, California, USA.
  • 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, Stanford University, Stanford, California, USA.
  • 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, Stanford University School of Medicine, Stanford, California, USA.
  • Regula DP; Department of Pathology, Stanford University School of Medicine, Stanford, California, USA.
  • Pacheco-Navarro AE; Department of Pathology, Stanford University School of Medicine, Stanford, California, USA.
  • Yang S; Department of Pulmonology, Allergy and Critical Care Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • 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, Stanford University School of Medicine, Stanford, California, USA.
  • Peters AM; Department of Biochemistry and Molecular Biology, University of Texas Health Science Center - McGovern Medical School, Houston, Texas, USA.
  • Zhao B; Divisions of Critical Care, Pulmonary and Sleep Medicine, Department of Internal Medicine, University of Texas Health Science Center - McGovern Medical School, Houston, Texas, USA.
  • Buja ML; Department of Biochemistry and Molecular Biology, University of Texas Health Science Center - McGovern Medical School, Houston, Texas, USA.
  • Johnson PY; Department of Pathology and Laboratory Medicine, Department of Internal Medicine, University of Texas Health Science Center - McGovern Medical School, Houston, Texas, USA.
  • Vernon RB; Department of Pathology and Laboratory Medicine, Department of Internal Medicine, University of Texas Health Science Center - McGovern Medical School, Houston, Texas, USA.
  • Wight TN; Matrix Biology Program, Benaroya Research Institute, Seattle, Washington, USA.
  • Milla CE; Matrix Biology Program, Benaroya Research Institute, Seattle, Washington, USA.
  • Spakowitz AJ; Center for Excellence in Pulmonary Biology, Department of Pediatrics, Stanford University, Stanford, California, USA.
  • Heilshorn SC; Department of Pulmonology, Allergy and Critical Care Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Bollyky PL; Department of Chemical Engineering, Stanford University, Stanford, California, USA.
medRxiv ; 2022 Apr 04.
Article em En | MEDLINE | ID: mdl-35411348
ABSTRACT
Thick, viscous respiratory secretions are a major pathogenic feature of COVID-19 disease, 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 find the percent solids and protein content are greatly elevated in COVID-19 compared to heathy control samples and closely resemble levels seen in cystic fibrosis, a genetic disease known for thick, tenacious respiratory secretions. DNA and hyaluronan (HA) are major components of respiratory secretions in COVID-19 and are likewise abundant in cadaveric lung tissues from these patients. COVID-19 secretions exhibit heterogeneous rheological behaviors with thicker samples showing increased sensitivity to DNase and hyaluronidase treatment. In histologic sections from these same patients, we observe increased accumulation of HA and the hyaladherin versican but reduced tumor necrosis factorâ€"stimulated gene-6 (TSG6) 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 indicate that increases in HA and DNA in COVID-19 respiratory secretion samples correlate with enhanced inflammatory burden and suggest that DNA and HA may be viable therapeutic targets in COVID-19 infection.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article