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Proteins of the cystic fibrosis respiratory tract. Fragmented immunoglobulin G opsonic antibody causing defective opsonophagocytosis.

In the disease cystic fibrosis (CF), pulmonary infection with Pseudomonas aeruginosa is a common clinical complication that determines most morbidity and almost all excess mortality. We postulated that in this disease a defect in Pseudomonas-reactive IgG antibodies may contribute to chronic Pseudomo...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:J Clin Invest
Päätekijät: Fick, R B, Naegel, G P, Squier, S U, Wood, R E, Gee, J B, Reynolds, H Y
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: American Society for Clinical Investigation 1984
Aiheet:
Linkit:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC425206/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6429195/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI111407
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