High levels of complement-activation capacity in sera from patients with cystic fibrosis correlate with high levels of IgG3 antibodies to Pseudomonas aeruginosa antigens and poor lung function.

Pressler, T; Jensen, E T; Espersen, F; Pedersen, S S; Høiby, N

Pressler, T; Jensen, E T; Espersen, F; Pedersen, S S; Høiby, N.

Affiliation

Pressler T; Danish CF Center, Department of Paediatrics, Rigshospitalet, Copenhagen, Denmark.

Pediatr Pulmonol ; 20(2): 71-7, 1995 Aug.

Article in En | MEDLINE | ID: mdl-8570305

Subject(s)

Antigens, Bacterial/immunology; Complement Activation/immunology; Complement System Proteins/metabolism; Cystic Fibrosis/immunology; Immunoglobulin G/blood; Pseudomonas aeruginosa/immunology; Adolescent; Adult; Cross-Sectional Studies; Humans; Longitudinal Studies

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Pseudomonas aeruginosa / Complement System Proteins / Immunoglobulin G / Complement Activation / Cystic Fibrosis / Antigens, Bacterial Type of study: Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Adolescent / Adult / Humans Language: En Journal: Pediatr Pulmonol Journal subject: PEDIATRIA Year: 1995 Document type: Article Affiliation country: Denmark

Search on Google

Add to My VHL

XML

PubMed Links