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Personalized bacteriophage therapy outcomes for 100 consecutive cases: a multicentre, multinational, retrospective observational study

噬菌体 医学 噬菌体疗法 内科学 抗生素 观察研究 回顾性队列研究 优势比 不利影响 置信区间 抗生素耐药性 微生物学 生物 生物化学 大肠杆菌 基因
作者
Jean‐Paul Pirnay,Sarah Djebara,Griet Steurs,Johann Griselain,Christel Cochez,Steven De Soir,Téa Glonti,An Spiessens,Emily Vanden Berghe,Sabrina I. Green,Jeroen Wagemans,Cédric Lood,Eddie Schrevens,Ніна Чанішвілі,Mzia Kutateladze,Mathieu de Jode,Pieter‐Jan Ceyssens,Jean‐Pierre Draye,Gilbert Verbeken,Daniël De Vos
出处
期刊:Nature microbiology [Nature Portfolio]
卷期号:9 (6): 1434-1453 被引量:244
标识
DOI:10.1038/s41564-024-01705-x
摘要

Abstract In contrast to the many reports of successful real-world cases of personalized bacteriophage therapy (BT), randomized controlled trials of non-personalized bacteriophage products have not produced the expected results. Here we present the outcomes of a retrospective observational analysis of the first 100 consecutive cases of personalized BT of difficult-to-treat infections facilitated by a Belgian consortium in 35 hospitals, 29 cities and 12 countries during the period from 1 January 2008 to 30 April 2022. We assessed how often personalized BT produced a positive clinical outcome (general efficacy) and performed a regression analysis to identify functional relationships. The most common indications were lower respiratory tract, skin and soft tissue, and bone infections, and involved combinations of 26 bacteriophages and 6 defined bacteriophage cocktails, individually selected and sometimes pre-adapted to target the causative bacterial pathogens. Clinical improvement and eradication of the targeted bacteria were reported for 77.2% and 61.3% of infections, respectively. In our dataset of 100 cases, eradication was 70% less probable when no concomitant antibiotics were used (odds ratio = 0.3; 95% confidence interval = 0.127–0.749). In vivo selection of bacteriophage resistance and in vitro bacteriophage–antibiotic synergy were documented in 43.8% (7/16 patients) and 90% (9/10) of evaluated patients, respectively. We observed a combination of antibiotic re-sensitization and reduced virulence in bacteriophage-resistant bacterial isolates that emerged during BT. Bacteriophage immune neutralization was observed in 38.5% (5/13) of screened patients. Fifteen adverse events were reported, including seven non-serious adverse drug reactions suspected to be linked to BT. While our analysis is limited by the uncontrolled nature of these data, it indicates that BT can be effective in combination with antibiotics and can inform the design of future controlled clinical trials. BT100 study, ClinicalTrials.gov registration: NCT05498363 .
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