Abstract
EPI-hNE4 (depelstat) is a potent inhibitor of human neutrophil elastase derived from human inter-α-trypsin inhibitor and designed to control the excess proteolytic activity in the sputum of cystic fibrosis patients. We analyzed its resistance to the proteolysis it is likely to encounter at inflammatory sites in vivo. EPI-hNE4 resisted hydrolysis by neutrophil matrix metalloproteases (MMPs) and serine proteases that are released from activated neutrophils in inflammatory lung secretions, including MMP-8 and MMP-9, and the elastase-related protease 3 and cathepsin G. It also resisted degradation by epithelial lung cell MMP-7 but was broken down by the Pseudomonas aeruginosa metalloelastase pseudolysin, when used in a purified system, but not when this protease competed with equimolar amounts of neutrophil elastase. We also investigated the inhibitory properties of EPI-hNE4 at the surface of purified blood neutrophils and in the sputum of cystic fibrosis patients where neutrophil elastase is in both a soluble and a gel phase. The elastase at the neutrophil surface was fully inhibited by EPI-hNE4 and formed soluble complexes. The elastase in cystic fibrosis sputum supernatants was inhibited by stoichiometric amounts of EPI-hNE4, allowing titration of the protease. But the percentage of inhibition in whole sputum homogenates varied from 50 to 100%, depending on the sample tested. EPI-hNE4 was rapidly cleaved by the digestive protease pepsin in vitro. Therefore, EPI-hNE4 seems to be an elastase inhibitor suitable for use in aerosols to treat patients with cystic fibrosis.
Footnotes
-
This work was supported by the Association “Vaincre La Mucoviscidose” (France) and Debiopharm S.A. (Lausanne, Switzerland).
-
Article, publication date, and citation information can be found at http://jpet.aspetjournals.org.
-
doi:10.1124/jpet.106.103440.
-
ABBREVIATIONS: CF, cystic fibrosis; HNE, human neutrophil elastase; Pr3, protease 3; cat G, cathepsin G; IL, interleukin; MMP, matrix metalloprotease; α1-PI, α1-protease inhibitor; PBS, phosphate-buffered saline; Abz, ortho-aminobenzoic acid; EDDnp, N-(2,4-dinitrophenyl)ethylenediamine; Tricine, N-[2-hydroxy-1,1-bis(hydroxymethyl)ethyl]glycine; mHNE, membrane-bound HNE; HPLC, high-performance liquid chromatography; SLPI, secretory leukocyte protease inhibitor; EPI-hNE4, depelstat.
- Received February 24, 2006.
- Accepted April 19, 2006.
- The American Society for Pharmacology and Experimental Therapeutics
JPET articles become freely available 12 months after publication, and remain freely available for 5 years.Non-open access articles that fall outside this five year window are available only to institutional subscribers and current ASPET members, or through the article purchase feature at the bottom of the page.
|