Literature DB >> 1671425

Aerosol alpha 1-antitrypsin treatment for cystic fibrosis.

N G McElvaney1, R C Hubbard, P Birrer, M S Chernick, D B Caplan, M M Frank, R G Crystal.   

Abstract

In cystic fibrosis neutrophil-dominated inflammation on the respiratory epithelial surface results in a chronic epithelial burden of the destructive enzyme, neutrophil elastase. alpha 1-antitrypsin (alpha 1AT), the main inhibitor of neutrophil elastase in lung, was given in aerosol form to 12 cystic fibrosis patients. It suppressed neutrophil elastase in the respiratory epithelial lining fluid (ELF) and restored the ELF anti-neutrophil elastase capacity when ELF alpha 1AT reached 8 mumol/l. This treatment also reversed the inhibitory effect of cystic fibrosis ELF on pseudomonas killing by neutrophils, which suggests that it may augment host defence in cystic fibrosis.

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Year:  1991        PMID: 1671425     DOI: 10.1016/0140-6736(91)91167-s

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  71 in total

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Review 6.  Use of modulators of airways inflammation in patients with CF.

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8.  Immunization with Pseudomonas aeruginosa vaccines and adjuvant can modulate the type of inflammatory response subsequent to infection.

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Review 9.  New perspectives in understanding and management of the respiratory disease in cystic fibrosis.

Authors:  S Suter
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10.  Sputum biomarkers of inflammation and lung function decline in children with cystic fibrosis.

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