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DOI 10.1136/adc.67.6.737

Медицинская библиотека · Archives of disease in childhood · 1992

IgG antibodies in early Pseudomonas aeruginosa infection in cystic fibrosis.

Cordon S M, Elborn J S, Rayner R J, Hiller E J, Shale D J

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

The relationship between IgG antibodies to Pseudomonas aeruginosa and its isolation from sputum was determined in 100 patients with cystic fibrosis observed at intervals of two months for a median period of one year. Only one patient had a raised antibody titre (greater than 22.9 ELISA units) before isolation of P aeruginosa. Initially 65 patients were antibody negative, of whom 48 were also culture negative. Of 24 patients with positive sputum culture and negative antibodies, seven became antibody positive at a median (range) 15 (6-25) months later. The remaining 17 patients continued antibody negative until the end of the study at a median range 15 (1-123) months after becoming culture positive. This latter group were younger and had more intermittently positive sputum cultures. In general positive IgG antibody titres do not predate isolation of P aeruginosa, but in some patients are present soon after acquisition of infection. A positive titre indicates significant exposure to P aeruginosa and could be used to detect infection in patients unable to produce sputum and possibly indicate the effect of early antipseudomonal treatment.

Для цитирования: Cordon S M, Elborn J S, Rayner R J, Hiller E J, Shale D J. IgG antibodies in early Pseudomonas aeruginosa infection in cystic fibrosis.. Archives of disease in childhood. 1992. DOI: 10.1136/adc.67.6.737.

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