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Immunoglobulin A and immunoglobulin G antibody responses to alginates from Pseudomonas aeruginosa in patients with cystic fibrosis.

Patients with cystic fibrosis have a high prevalence of mucoid, alginate-producing Pseudomonas aeruginosa that causes chronic infection of the mucosal surface of the lungs. We developed enzyme-linked immunosorbent assays (ELISAs) for determination in serum of immunoglobulin A (IgA) and IgG antibodie...

Ausführliche Beschreibung

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Bibliografische Detailangaben
Veröffentlicht in:J Clin Microbiol
Hauptverfasser: Pedersen, S S, Espersen, F, Høiby, N, Jensen, T
Format: Artigo
Sprache:Inglês
Veröffentlicht: American Society for Microbiology (ASM) 1990
Schlagworte:
Online-Zugang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC267788/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2110181/
https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jcm.28.4.747-755.1990
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