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Biotechnol Appl Biochem ; 59(1): 22-8, 2012.
Article in English | MEDLINE | ID: mdl-22332741

ABSTRACT

PRT-201 is a recombinant human pancreatic elastase under development as a treatment for blood vessels to promote hemodialysis access patency. Proteases such as elastase are normally inactivated by antiproteases such as alpha 1-antitrypsin. It is unknown if serum from patients with alpha 1-antitrypsin deficiency will inhibit PRT-201 elastase activity. An assay for PRT-201 elastase activity in the presence of serum was developed and validated. PRT-201 elastase activity inhibition curves were developed using serum and also using purified alpha 1-antitrypsin and alpha 2-macroglobulin. Serum from 15 patients with documented alpha 1-antitrypsin deficiency, some of whom were receiving alpha 1-antitrypsin augmentation therapy, and four normal volunteers was analyzed. Serum from normal volunteers and patients with alpha 1-antitrypsin deficiency completely inactivated PRT-201 elastase activity in vitro. In the alpha 1-antitrypsin-deficient patients, the volume of serum necessary to inhibit elastase activity was related to the serum concentration of alpha 1-antitrypsin and augmentation therapy. Purified alpha 1-antitrypsin and alpha 2-macroglobulin were each alone capable of completely inhibiting PRT-201 elastase activity. It is unlikely that the use of PRT-201 will be associated with negative outcomes in patients with alpha 1-antitrypsin deficiency.


Subject(s)
Pancreatic Elastase/antagonists & inhibitors , Serum , alpha 1-Antitrypsin Deficiency/blood , Adult , Aged , Diabetes Mellitus, Type 1/enzymology , Female , Humans , Male , Middle Aged , Pancreatic Elastase/metabolism , Recombinant Proteins/antagonists & inhibitors , Recombinant Proteins/metabolism , alpha 1-Antitrypsin Deficiency/metabolism
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