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首个将粪便微生物群移植用作治疗感染的药用产品的英国粪便库的结果。

Results from the first English stool bank using faecal microbiota transplant as a medicinal product for the treatment of infection.

作者信息

McCune V L, Quraishi M N, Manzoor S, Moran C E, Banavathi K, Steed H, Massey D C O, Trafford G R, Iqbal T H, Hawkey P M

机构信息

Public Health England, Public Health Laboratory Birmingham, University Hospitals Birmingham NHS Foundation Trust, Heartlands Hospital, Bordesley Green East, Birmingham B5 9SS, England.

Institute of Microbiology and Infection, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TH, England.

出版信息

EClinicalMedicine. 2020 Mar 16;20:100301. doi: 10.1016/j.eclinm.2020.100301. eCollection 2020 Mar.

Abstract

BACKGROUND

Faecal Microbiota Transplant (FMT) has improved outcomes for the treatment of infection (CDI) compared to antibiotic therapy. FMT is classified as a medicinal product in the United Kingdom, similar to the USA and Canada, limiting supply via stool banks without appropriate licencing. In the largest UK cohort to date, we describe the clinical outcomes for 124 patients receiving FMT for recurrent or refractory CDI and present a framework to produce FMT as a licenced medicinal product.

METHODS

Anonymous unrelated healthy donors, screened via health assessment and microbiological testing donated stool. In aerobic conditions FMT aliquots were prepared for immediate use or frozen storage, following a production framework developed to comply with Good Manufacturing Practice. Outcome measures were clinical response to FMT defined as resolution of diarrhoea within seven days and clinical cure defined as response without diarrhoea recurrence at 90 days.

FINDINGS

Clinical response was 83·9% (95% CI 76·0%-90·0%) after one treatment. Clinical cure was 78·2% (95% CI 67·4%-89·0%) across the cohort. Refractory cases appeared to have a lower initial clinical response rate compared to recurrent cases, however at day 90 there were no differences observed between these groups.

INTERPRETATION

The methodology developed here enabled successful licencing of FMT by The Medicines and Healthcare products Regulatory Agency as a medicinal product. This has widened the availability of FMT in the National Health Service via a stool bank and can be applied in other centres across the world to improve access to safe and quality assured treatments.

摘要

背景

与抗生素治疗相比,粪便微生物群移植(FMT)改善了艰难梭菌感染(CDI)的治疗效果。在英国,FMT与美国和加拿大一样被归类为药品,这限制了未经适当许可的粪便库的供应。在英国迄今为止最大的队列研究中,我们描述了124例接受FMT治疗复发性或难治性CDI患者的临床结局,并提出了一个将FMT生产为有许可证药品的框架。

方法

通过健康评估和微生物检测筛选出的匿名无关健康供体捐赠粪便。在有氧条件下,按照为符合良好生产规范而制定的生产框架,制备FMT等分试样以供立即使用或冷冻保存。结局指标为对FMT的临床反应,定义为7天内腹泻缓解;临床治愈定义为90天内无腹泻复发。

研究结果

一次治疗后的临床反应率为83.9%(95%CI 76.0%-90.0%)。整个队列的临床治愈率为78.2%(95%CI 67.4%-89.0%)。与复发性病例相比,难治性病例的初始临床反应率似乎较低,然而在第90天时,这些组之间未观察到差异。

解读

此处开发的方法使药品和保健品监管局成功将FMT许可为一种药品。这通过粪便库扩大了FMT在国民医疗服务体系中的可及性,并且可应用于世界各地的其他中心,以改善获得安全且质量有保证的治疗的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/402b/7152830/f385811b81f6/gr1.jpg

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