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益生菌治疗作为 COVID-19 暴露后预防的疗效:一项双盲、安慰剂对照随机试验。

Efficacy of probiotic treatment as post-exposure prophylaxis for COVID-19: A double-blind, Placebo-Controlled Randomized trial.

机构信息

Duke University School of Medicine, Department of Anesthesiology, Durham, NC, USA.

Duke University School of Medicine, Durham, NC, USA.

出版信息

Clin Nutr. 2024 Jan;43(1):259-267. doi: 10.1016/j.clnu.2023.11.043. Epub 2023 Dec 11.

Abstract

BACKGROUND & AIMS: The COVID-19 pandemic continues to pose unprecedented challenges to worldwide health. While vaccines are effective, additional strategies to mitigate the spread/severity of COVID-19 continue to be needed. Emerging evidence suggests susceptibility to respiratory tract infections in healthy subjects can be reduced by probiotic interventions; thus, probiotics may be a low-risk, low-cost, and easily implementable modality to reduce risk of COVID-19.

METHODS

In this initial study, we conducted a randomized, double-blind, placebo-controlled trial across the United States testing probiotic Lacticaseibacillus rhamnosus GG (LGG) as postexposure prophylaxis for COVID-19 in 182 participants who had household exposure to someone with confirmed COVID-19 diagnosed within ≤7 days. Participants were randomized to receive oral LGG or placebo for 28 days. The primary outcome was development of illness symptoms within 28 days of COVID-19 exposure. Stool was collected to evaluate microbiome changes.

RESULTS

Intention-to-treat analysis showed LGG treatment led to a lower likelihood of developing illness symptoms versus placebo (26.4 % vs. 42.9 %, p = 0.02). Further, LGG was associated with a statistically significant reduction in COVID-19 diagnosis (log rank, p = 0.049) via time-to-event analysis. Overall incidence of COVID-19 diagnosis did not significantly differ between LGG and placebo groups (8.8 % vs. 15.4 %, p = 0.17).

CONCLUSIONS

This data suggests LGG is associated with prolonged time to COVID-19 infection, reduced incidence of illness symptoms, and gut microbiome changes when used as prophylaxis ≤7 days post-COVID-19 exposure, but not overall incidence. This initial work may inform future COVID-19 prevention studies worldwide, particularly in developing nations where Lacticaseibacillus probiotics have previously been utilized to reduce other non-COVID infectious-morbidity.

TRIAL REGISTRATION

ClinicalTrials.gov, NCT04399252, Date: 22/05/2020. https://clinicaltrials.gov/ct2/show/NCT04399252.

摘要

背景与目的

新冠疫情继续对全球健康构成前所未有的挑战。疫苗虽然有效,但仍需要采取其他策略来减轻新冠疫情的传播和严重程度。新出现的证据表明,通过益生菌干预可以降低健康受试者呼吸道感染的易感性;因此,益生菌可能是一种低风险、低成本且易于实施的方式,可以降低感染新冠病毒的风险。

方法

在这项初步研究中,我们在美国进行了一项随机、双盲、安慰剂对照试验,试验对象为 182 名参与者,他们的家中有人在确诊新冠病毒感染后 7 天内被确诊。参与者被随机分为口服罗伊氏乳杆菌 GG(LGG)或安慰剂组,进行 28 天的治疗。主要结局是在接触新冠病毒后 28 天内出现疾病症状。收集粪便样本以评估微生物组的变化。

结果

意向治疗分析显示,与安慰剂组相比,LGG 治疗组出现疾病症状的可能性较低(26.4% vs. 42.9%,p=0.02)。此外,通过时间事件分析,LGG 与新冠病毒诊断的显著降低相关(对数秩检验,p=0.049)。LGG 组和安慰剂组的新冠病毒诊断总体发生率无显著差异(8.8% vs. 15.4%,p=0.17)。

结论

这些数据表明,在新冠病毒暴露后≤7 天内使用 LGG 进行预防,与延长新冠病毒感染时间、降低疾病症状发生率以及肠道微生物组变化相关,但与总体发生率无关。这项初步研究结果可能为全球范围内的新冠病毒预防研究提供信息,特别是在发展中国家,此前曾使用乳杆菌益生菌来降低其他非新冠病毒的传染性疾病发病率。

试验注册

ClinicalTrials.gov,NCT04399252,日期:2020 年 5 月 22 日。https://clinicaltrials.gov/ct2/show/NCT04399252。

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