Proteins of the cystic fibrosis respiratory tract. Fragmented immunoglobulin G opsonic antibody causing defective opsonophagocytosis
about
Measurements of Deposition, Lung Surface Area and Lung Fluid for Simulation of Inhaled CompoundsNeutrophil plasticity enables the development of pathological microenvironments: implications for cystic fibrosis airway diseaseComparison of fluorescence-based methods to determine nanoparticle uptake by phagocytes and non-phagocytic cells in vitro.Serine proteinase inhibitor therapy in alpha(1)-antitrypsin inhibitor deficiency and cystic fibrosis.Effect of nebulised recombinant DNase on neutrophil elastase load in cystic fibrosis.Pseudomonas aeruginosa-induced lung and pleural injury in sheep. Differential protective effect of circulating versus alveolar immunoglobulin G antibody.Neutrophil elastase, proteinase 3, and cathepsin G as therapeutic targets in human diseases.Pseudomonas and neutrophil products modify transferrin and lactoferrin to create conditions that favor hydroxyl radical formation.Protease-cleaved iron-transferrin augments oxidant-mediated endothelial cell injury via hydroxyl radical formation.Neutrophil elastase cleaves C3bi on opsonized pseudomonas as well as CR1 on neutrophils to create a functionally important opsonin receptor mismatch.The immunoglobulin G subclass composition of immune complexes in cystic fibrosis. Implications for the pathogenesis of the Pseudomonas lung lesionClinical significance of microbial infection and adaptation in cystic fibrosis.Role of interleukin-8 (IL-8) and an inhibitory effect of erythromycin on IL-8 release in the airways of patients with chronic airway diseases.Alpha-1 proteinase inhibitors for the treatment of alpha-1 antitrypsin deficiency: safety, tolerability, and patient outcomes.Human neutrophil elastase induces hypersecretion of mucin from well-differentiated human bronchial epithelial cells in vitro via a protein kinase C{delta}-mediated mechanism.Intravenous immunoglobulin for cystic fibrosis lung disease: a case series of 16 children.Penetration of cefotaxime into respiratory secretions.Neutrophil elastase in respiratory epithelial lining fluid of individuals with cystic fibrosis induces interleukin-8 gene expression in a human bronchial epithelial cell line.Modulation of airway inflammation in cystic fibrosis. In vivo suppression of interleukin-8 levels on the respiratory epithelial surface by aerosolization of recombinant secretory leukoprotease inhibitor.SerpinB1 in cystic fibrosis airway fluids: quantity, molecular form and mechanism of elastase inhibition.Complement receptor expression on neutrophils at an inflammatory site, the Pseudomonas-infected lung in cystic fibrosis.Microbiology of airway disease in patients with cystic fibrosis.Oxidative regulation of neutrophil elastase-alpha-1-proteinase inhibitor interactionsCandidacidal factors in murine bronchoalveolar lavage fluidPseudomonas aeruginosa adhesins for tracheobronchial mucin.Opsonophagocytic killing activity of rabbit antibody to Pseudomonas aeruginosa mucoid exopolysaccharideInterfering with extracellular matrix degradation to blunt inflammationProteases and cystic fibrosis.The role of proteases, endoplasmic reticulum stress and SERPINA1 heterozygosity in lung disease and α-1 anti-trypsin deficiency.Immune responses in cystic fibrosis: are they intrinsically defective?The Pseudomonas aeruginosa secretory product pyocyanin inactivates alpha1 protease inhibitor: implications for the pathogenesis of cystic fibrosis lung disease.Protease cleavage of iron-transferrin augments pyocyanin-mediated endothelial cell injury via promotion of hydroxyl radical formation.Phenotypic conversion of Pseudomonas aeruginosa in cystic fibrosis.Transferrin and lactoferrin undergo proteolytic cleavage in the Pseudomonas aeruginosa-infected lungs of patients with cystic fibrosis.Effector mechanisms of intestinally induced immunity to Pseudomonas aeruginosa in the rat lung: role of neutrophils and leukotriene B4Nonopsonic antibodies in cystic fibrosis. Pseudomonas aeruginosa lipopolysaccharide-specific immunoglobulin G antibodies from infected patient sera inhibit neutrophil oxidative responses.Interleukin-8 up-regulation by neutrophil elastase is mediated by MyD88/IRAK/TRAF-6 in human bronchial epithelium.The immunoevasive activities of Pseudomonas aeruginosa. Relevance for cystic fibrosis.Gcglobulin functions as a cochemotaxin in the lower respiratory tract. A potential mechanism for lung neutrophil recruitment in cigarette smokers.Role of microbial proteases in pathogenesis.
P2860
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P2860
Proteins of the cystic fibrosis respiratory tract. Fragmented immunoglobulin G opsonic antibody causing defective opsonophagocytosis
description
1984 nî lūn-bûn
@nan
1984 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1984 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1984年の論文
@ja
1984年論文
@yue
1984年論文
@zh-hant
1984年論文
@zh-hk
1984年論文
@zh-mo
1984年論文
@zh-tw
1984年论文
@wuu
name
Proteins of the cystic fibrosi ...... g defective opsonophagocytosis
@ast
Proteins of the cystic fibrosi ...... g defective opsonophagocytosis
@en
Proteins of the cystic fibrosi ...... g defective opsonophagocytosis
@nl
type
label
Proteins of the cystic fibrosi ...... g defective opsonophagocytosis
@ast
Proteins of the cystic fibrosi ...... g defective opsonophagocytosis
@en
Proteins of the cystic fibrosi ...... g defective opsonophagocytosis
@nl
prefLabel
Proteins of the cystic fibrosi ...... g defective opsonophagocytosis
@ast
Proteins of the cystic fibrosi ...... g defective opsonophagocytosis
@en
Proteins of the cystic fibrosi ...... g defective opsonophagocytosis
@nl
P2093
P2860
P356
P1476
Proteins of the cystic fibrosi ...... g defective opsonophagocytosis
@en
P2093
P2860
P304
P356
10.1172/JCI111407
P407
P577
1984-07-01T00:00:00Z