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...

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Publikašuvnnas:	J Clin Microbiol
Váldodahkkit:	Pedersen, S S, Espersen, F, Høiby, N, Jensen, T
Materiálatiipa:	Artigo
Giella:	Inglês
Almmustuhtton:	American Society for Microbiology (ASM) 1990
Fáttát:	Research Article
Liŋkkat:	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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