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Recombinant human DNase I reduces the viscosity of cystic fibrosis sputum.
Author(s) -
Steven Shak,
Daniel J. Capon,
Renate Hellmiss,
Scot A. Marsters,
Colleen Baker
Publication year - 1990
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.87.23.9188
Subject(s) - cystic fibrosis , sputum , recombinant dna , medicine , pancreatic disease , lung , respiratory distress , bronchitis , microbiology and biotechnology , pneumonia , chronic bronchitis , chemistry , immunology , biology , pathology , pancreas , anesthesia , biochemistry , gene , tuberculosis
Respiratory distress and progressive lung destruction in cystic fibrosis can be attributed to bacterial persistence and the accumulation of viscous purulent secretions in the airways. More than 30 yr ago it was suggested that the large amounts of DNA in purulent secretions contribute to its viscosity and that bovine pancreatic DNase I could reduce the viscosity. To evaluate the potential clinical utility of recombinant human DNase I (rhDNase) in the treatment of cystic fibrosis, we have cloned, sequenced, and expressed rhDNase. Catalytic amounts of rhDNase greatly reduce the viscosity of purulent cystic fibrosis sputum, transforming it within minutes from a nonflowing viscous gel to a flowing liquid. The reduction in viscosity is associated with a decrease in size of DNA in the sputum. Inhalation of a rhDNase aerosol may be a simple direct approach that will help individuals with cystic fibrosis and other patients with pneumonia or bronchitis to clear their airways of purulent secretions.

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