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DOI 10.1016/j.jcf.2012.04.010

Медицинская библиотека · Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2012

Increase in interleukin-8 production from circulating neutrophils upon antibiotic therapy in cystic fibrosis patients.

Montemurro Pasqualina, Mariggiò Maria A, Barbuti Giovanna, Cassano Amalia, Vincenti Alessandra, Serio Gabriella, Guerra Lorenzo, Diana Anna, Santostasi Teresa, Polizzi Angela, Fumarulo Ruggiero, Casavola Valeria, Manca Antonio, Conese Massimo

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

It is not known whether antibiotic therapy for lung disease in cystic fibrosis (CF) has an influence on circulating polymorphonuclear neutrophil (PMN) function and apoptosis.

PATIENTS AND

METHODS

Blood PMNs were obtained from 14 CF patients before and after antibiotic treatment for an acute exacerbation, and from 10 healthy controls. PMNs were evaluated for production of reactive oxygen species (ROS) by spectrophotometry, of cytokines in the conditioned medium by ELISA, and apoptotic response by cytofluorimetry.

RESULTS

ROS and interleukin (IL)-8 were produced at higher levels by CF PMNs pre-therapy than control PMNs under basal conditions. IL-8 levels further increased after therapy. Early apoptotic response was higher in CF PMNs pre-therapy than in control PMNs, and this pattern did not change after antibiotic treatment.

CONCLUSIONS

Circulating PMNs are primed in CF acute patients. Further studies are needed to consider PMN-produced IL-8 as a biomarker to evaluate response to antibiotic therapy in CF patients.

Для цитирования: Montemurro Pasqualina, Mariggiò Maria A, Barbuti Giovanna, Cassano Amalia, Vincenti Alessandra, Serio Gabriella, Guerra Lorenzo, Diana Anna, Santostasi Teresa, Polizzi Angela, Fumarulo Ruggiero, Casavola Valeria, Manca Antonio, Conese Massimo. Increase in interleukin-8 production from circulating neutrophils upon antibiotic therapy in cystic fibrosis patients.. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 2012. DOI: 10.1016/j.jcf.2012.04.010.

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