Children's Health and Environment Program, Child Health Research Centre, The University of Queensland, South Brisbane, Qld Australia.
Children's Health and Environment Program, Child Health Research Centre, The University of Queensland, South Brisbane, Qld Australia; Child and Reproductive Health Research Group, Queensland University of Technology, South Brisbane, Qld Australia.
J Cyst Fibros. 2022 Jul;21(4):707-712. doi: 10.1016/j.jcf.2021.12.015. Epub 2022 Jan 3.
Exaggerated neutrophil-dominated inflammation underlies progressive cystic fibrosis (CF) lung disease. Older studies reported a defective respiratory burst in CF, but more recent studies suggest neutrophil function is normal.
We measured the amount and rate of reactive oxygen species (ROS) during PMA-stimulated respiratory burst activity in children [70 CF, 13 disease controls, 19 health controls] and adults [31 CF, 14 health controls] in neutrophils harvested from peripheral blood. Blood was collected from participants with CF when clinically stable (60 children, 9 adults) and on hospital admission (38 children, 24 adults) and discharge (18 children, 21 adults) for acute pulmonary exacerbations.
When clinically stable, children with CF had lower ROS production [median 318,633, 25% 136,810 - 75% 569,523 RLU] than disease controls [median 599,459, 25% 425,566 - 75% 730,527 RLU] and healthy controls [median 534,073, 25% 334,057 - 75% 738,593 RLU] (p = 0.008). The rate of ROS production was also lower (p = 0.029). In neither children nor adults with CF did ROS production increase on hospital admission for acute pulmonary exacerbation, nor fall prior to discharge. There were no associations between ROS production and high-sensitivity C-reactive protein (indicating systemic inflammation) in either children or adults with CF.
Our data do not support a role for exaggerated respiratory burst activity contributing to the exaggerated neutrophil-dominated inflammation seen with CF lung disease.
在进行性囊性纤维化 (CF) 肺病中,过度的中性粒细胞主导的炎症是基础。早期的研究报告 CF 中存在呼吸爆发缺陷,但最近的研究表明中性粒细胞功能正常。
我们测量了儿童(70 例 CF、13 例疾病对照组、19 例健康对照组)和成人(31 例 CF、14 例健康对照组)外周血中性粒细胞在 PMA 刺激呼吸爆发活性时产生的活性氧(ROS)的数量和速率。当 CF 患者临床稳定时(60 例儿童,9 例成人)和因急性肺部加重入院时(38 例儿童,24 例成人)和出院时(18 例儿童,21 例成人)采集 CF 患者的血液。
当临床稳定时,CF 患儿的 ROS 产生量[中位数 318633,25% 136810-75% 569523 RLU]低于疾病对照组[中位数 599459,25% 425566-75% 730527 RLU]和健康对照组[中位数 534073,25% 334057-75% 738593 RLU](p=0.008)。ROS 的产生速度也较慢(p=0.029)。无论是儿童还是成人 CF 患者,急性肺部加重入院时 ROS 产生量并未增加,出院前也未减少。在 CF 患儿和成人中,ROS 产生量与高敏 C 反应蛋白(表示全身炎症)之间均无关联。
我们的数据不支持过度呼吸爆发活动导致 CF 肺部疾病中所见的过度中性粒细胞主导的炎症的作用。