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口服微生物群疗法——粪便微生物群孢子(活芽孢)预防成人感染复发的系统评价

Systematic review of the orally administered microbiome therapeutic, fecal microbiota spores, live-brpk, to prevent recurrence of infection in adults.

作者信息

LaPlante Kerry, Stevens Robert, Gonzales-Luna Anne J

机构信息

College of Pharmacy, University of Rhode Island, Kingston, RI, USA.

Seres Therapeutics Inc., Cambridge, MA, USA.

出版信息

SAGE Open Med. 2024 Oct 9;12:20503121241274192. doi: 10.1177/20503121241274192. eCollection 2024.

Abstract

BACKGROUND

infection (CDI) has been linked to over 200,000 cases of illness in hospitalized patients and over 20,000 deaths annually. Up to 25% of patients with an initial CDI episode will experience recurrent CDI (rCDI), which most commonly occurs in the first 8 weeks following antibiotic therapy. In patients with first or multiple rCDI, infection, the microbiome is similarly disrupted, which highlights the challenges of using antibiotics alone while underscoring the need for microbiome restoration regardless of the number of recurrences. In this systematic review, we describe the role of the gastrointestinal microbiome in CDI, and systematically review fecal microbiota spores, live-brpk (VOWST™; VOS for Vowst Oral Spores) for prevention of recurrence in rCDI.

METHODS

The PubMed database was searched using "recurrent infection" AND (SER-109 OR VOS) and limited to clinical trials. The search yielded 7 results: 3 articles describing 3 clinical trials (two Phase 3 trials (ECOSPOR III and ECOSPOR IV) and one Phase 2 trial (ECOSPOR)), 1 describing follow-up of ECOSPOR III, 1 describing a post hoc analysis of comorbidities in ECOSPOR III, and 2 describing health-related quality of life in ECOSPOR III.

RESULTS

Compared with placebo, VOS following standard-of-care antibiotics for CDI significantly reduced risk of recurrence at 8 weeks (relative risk, 0.32 (95% CI: 0.18-0.58);  < 0.001; number needed to treat: 4) with a tolerable safety profile; rCDI rates remained low through 24 weeks. The disrupted microbiome, secondary to/exacerbated by antibiotic treatment, was rapidly (i.e., Week 1) restored with VOS. Compared with placebo, VOS demonstrated greater improvements in health-related quality of life.

CONCLUSIONS

Clinical care of patients with rCDI now includes Food and Drug Administration-approved therapeutics to address microbiome restoration. Clinical trial evidence supports use of VOS following antibiotics and importance of microbiome restoration in rCDI.

摘要

背景

艰难梭菌感染(CDI)与每年超过20万例住院患者患病以及超过2万例死亡相关。高达25%的首次CDI发作患者会经历复发性CDI(rCDI),这最常发生在抗生素治疗后的前8周内。在首次或多次发生rCDI的患者中,微生物群同样受到破坏,这凸显了单独使用抗生素的挑战,同时也强调了无论复发次数多少都需要恢复微生物群的必要性。在本系统评价中,我们描述了胃肠道微生物群在CDI中的作用,并系统评价了粪便微生物群孢子、活孢子(VOWST™;Vowst口服孢子的VOS)预防rCDI复发的作用。

方法

使用“复发性艰难梭菌感染”和(SER-109或VOS)在PubMed数据库中进行检索,并限于临床试验。检索结果有7条:3篇文章描述了3项临床试验(两项3期试验(ECOSPOR III和ECOSPOR IV)和一项2期试验(ECOSPOR)),1篇描述了ECOSPOR III的随访情况,1篇描述了ECOSPOR III中共病的事后分析,2篇描述了ECOSPOR III中与健康相关的生活质量。

结果

与安慰剂相比,在CDI的标准治疗抗生素之后使用VOS可显著降低8周时的复发风险(相对风险,0.32(95%CI:0.18-0.58);P<0.001;治疗所需人数:4),且安全性可耐受;rCDI率在24周内一直较低。抗生素治疗继发或加剧的微生物群紊乱通过VOS迅速(即第1周)得到恢复。与安慰剂相比,VOS在与健康相关的生活质量方面有更大改善。

结论

rCDI患者的临床护理现在包括美国食品药品监督管理局批准的用于恢复微生物群的治疗方法。临床试验证据支持在抗生素治疗后使用VOS以及微生物群恢复在rCDI中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1e/11462573/c99f786ab44a/10.1177_20503121241274192-fig1.jpg

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