Specific IgG2 antibodies toPseudomonas aeruginosa lipid A and lipopolysaccharide are early markers of chronic infection in patients with cystic fibrosis

This publication has 32 references indexed in Scilit:

• Cytokines in sputum and serum from patients with cystic fibrosis and chronic pseudomonas aeruginosa infection as markers of destructive inflammation in the lungs.
  Pediatric Pulmonology, 1993
• Antibodies from chronically infected cystic fibrosis patients react with lipopolysaccharides extracted by new micromethods from all serotypes of Pseudomonas aeruginosa
  APMIS, 1993
• IgG subclass antibody responses to alginate from Pseudomonas aeruginosa in patients with cystic fibrosis and chronic P. aeruginosa infection
  Pediatric Pulmonology, 1992
• Lipopolysaccharide is present in immune complexes isolated from sputum in patients with cystic fibrosis and chronic Pseudomonas aeruginosa lung infection
  APMIS, 1992
• Prevalence and persistence of polyagglutinable Pseudomonas aeruginosa in isolates from cystic fibrosis patients
  APMIS, 1991
• The immunoglobulin G subclass composition of immune complexes in cystic fibrosis. Implications for the pathogenesis of the Pseudomonas lung lesion.
  Journal of Clinical Investigation, 1990
• IgG subclass antibodies toPseudomonas aeruginosain sera from patients with chronicPs. aeruginosainfection investigated by ELISA
  Clinical and Experimental Immunology, 1990
• Determination of the components of immune complexes made in vitro with antigens derived from Pseudomonas aeruginosa
  Journal of Immunological Methods, 1989
• Lipoid A-Antikörpertiter beim Menschen
  Infection, 1987
• Interaction of Lipopolysaccharides and Lipid A with Complement
  European Journal of Biochemistry, 1971