Department of Respiratory Sciences, Institute for Lung Health, National Institute for Health Research Biomedical Research Centre, University of Leicester, Leicester, UK.
Clinical Respiratory Management, MedImmune Ltd., Cambridge, UK.
Int J Chron Obstruct Pulmon Dis. 2019 Jun 5;14:1177-1185. doi: 10.2147/COPD.S198302. eCollection 2019.
We hypothesized whether the reduction in eosinophilic airway inflammation in patients with chronic obstructive pulmonary disease (COPD) following treatment with benralizumab, a humanized, afucosylated, monoclonal antibody that binds to interleukin-5 receptor α, increases the airway bacterial load. Analysis of sputum samples of COPD patients participating in a Phase II trial of benralizumab indicated that sputum 16S rDNA load and were reduced following treatment with benralizumab. However, in vitro, eosinophils did not affect the killing of the common airway pathogens or . Thus, benralizumab may have an indirect effect upon airway bacterial load.
我们假设,在接受靶向白细胞介素-5 受体 α 的人源化去岩藻糖基化单克隆抗体贝那利珠单抗治疗后,慢性阻塞性肺疾病(COPD)患者嗜酸性气道炎症减少是否会增加气道细菌负荷。对参与贝那利珠单抗 II 期临床试验的 COPD 患者的痰样本进行的分析表明,贝那利珠单抗治疗后痰 16S rDNA 负荷和 减少。然而,在体外,嗜酸性粒细胞不会影响常见气道病原体 和 的杀伤。因此,贝那利珠单抗可能对气道细菌负荷有间接影响。