Baumann U, Fischer J J, Gudowius P, Lingner M, Herrmann S, Tümmler B, von der Hardt H
Dept. of Pediatric Pneumology and Neonatology, Hannover Medical School, Germany.
Infection. 2001 Jan-Feb;29(1):7-11. doi: 10.1007/s15010-001-0031-3.
The oropharyngeal barrier is an innate host defence mechanism to prevent bacterial Lung infection. A compromised barrier function is observed in patients with cystic fibrosis (CF) who are chronically infected with Pseudomonas aeruginosa. Macrolides are assumed to modify host defence. We investigated the oropharyngeaL barrier function in CF patients treated with azithromycin (AZM).
In a prospective study, eleven chronically infected children with CF were treated with longterm low-dose AZM. The oropharyngeal barrier function was assessed by adherence of P. aeruginosa (strain PACF 12-1) to buccal epithelial cells of the patients before and after therapy.
The mean (standard deviation, SD) buccaL adherence before therapy was markedly high with 8.0 (4.8) bacteria/cell. Following therapy with AZM adherence decreased in all patients by 70% or 5.6 to 2.4 (1.1) bacteria/cell (p = 0.007), representing close to normal LeveLs (1.2 +/- 0.6).
Long-term low-dose AZM therapy may improve the compromised oropharyngeaL barrier function in patients with CF, opening new perspectives for early treatment of P. aeruginosa infection in CF.
口咽屏障是一种先天性宿主防御机制,可预防肺部细菌感染。在长期感染铜绿假单胞菌的囊性纤维化(CF)患者中观察到屏障功能受损。大环内酯类药物被认为可改变宿主防御功能。我们研究了接受阿奇霉素(AZM)治疗的CF患者的口咽屏障功能。
在一项前瞻性研究中,11名长期感染CF的儿童接受了长期低剂量AZM治疗。通过治疗前后铜绿假单胞菌(菌株PACF 12-1)对患者颊上皮细胞的黏附来评估口咽屏障功能。
治疗前平均(标准差,SD)颊部黏附率显著较高,为8.0(4.8)个细菌/细胞。接受AZM治疗后,所有患者的黏附率均下降了70%,即从5.6降至2.4(1.1)个细菌/细胞(p = 0.007),接近正常水平(1.2±0.6)。
长期低剂量AZM治疗可能改善CF患者受损的口咽屏障功能,为CF患者铜绿假单胞菌感染的早期治疗开辟了新的前景。