益生菌能减轻艾滋病病毒感染者的炎症和增强肠道免疫健康吗:针对炎症和易位的益生菌Visbiome (prov IT)试点试验的研究设计

Q2 Medicine
HIV Clinical Trials Pub Date : 2016-07-01 Epub Date: 2016-06-07 DOI:10.1080/15284336.2016.1184827
Connie J Kim, Sharon L Walmsley, Janet M Raboud, Colin Kovacs, Bryan Coburn, Rodney Rousseau, Robert Reinhard, Ron Rosenes, Rupert Kaul
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引用次数: 30

摘要

目标:尽管联合抗逆转录病毒治疗(cART)在艾滋病毒预后方面有了实质性改善,但发病率和死亡率仍高于人群标准。肠道黏膜免疫系统不能完全通过cART恢复,由此产生的微生物易位可能导致慢性炎症,CD4 t细胞恢复不足,并增加严重非艾滋病事件的发生率。由于CD4 T细胞周围的微生物环境可能会影响其发育和功能,我们假设在cART过程中提供的益生菌可能会减少炎症并改善hiv阳性treatment-naïve个体(证明IT I)和cART中CD4恢复不佳的个体(证明IT II)的肠道免疫健康。这些前瞻性、双盲、随机、安慰剂对照、多中心的试点研究将评估益生菌Visbiome每天对9000亿细菌的影响。40名HIV阳性cART-naïve男性将在provov IT I研究中随机选取,同时开始抗逆转录病毒治疗,并随访24周。在proof IT II中,36名接受cART治疗的男性,但CD4 t细胞计数低于350细胞/毫米(3),将随访48周。两项研究的主要结果是比较血液CD8 t细胞免疫活化。二次分析将包括比较血液炎症生物标志物、微生物易位、血液和肠道免疫学以及HIV水平、细菌群落组成、饮食、肠道通透性以及研究产品的安全性、依从性和耐受性。讨论:这些研究将评估益生菌作为一种安全且可耐受的治疗干预措施的能力,以减少艾滋病毒感染者的全身免疫激活并加速肠道免疫恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Can Probiotics Reduce Inflammation and Enhance Gut Immune Health in People Living with HIV: Study Designs for the Probiotic Visbiome for Inflammation and Translocation (PROOV IT) Pilot Trials.

Objectives: Despite substantial improvements in HIV outcomes with combination antiretroviral therapy (cART), morbidity and mortality remain above population norms. The gut mucosal immune system is not completely restored by cART, and the resultant microbial translocation may contribute to chronic inflammation, inadequate CD4 T-cell recovery, and increased rates of serious non-AIDS events. Since the microbial environment surrounding a CD4 T cell may influence its development and function, we hypothesize that probiotics provided during cART might reduce inflammation and improve gut immune health in HIV-positive treatment-naïve individuals (PROOV IT I) and individuals with suboptimal CD4 recovery on cART (PROOV IT II).

Methods: These prospective, double-blinded, randomized, placebo-controlled, multicenter pilot studies will assess the impact of the probiotic Visbiome at 900 billion bacteria daily. Forty HIV positive cART-naïve men will be randomized in the PROOV IT I study, coincident with antiretroviral initiation, and be followed for 24 weeks. In PROOV IT II, 36 men on cART, but with a CD4 T-cell count below 350 cells/mm(3) will be followed for 48 weeks. The primary outcome for both studies is the comparison of blood CD8 T-cell immune activation. Secondary analyses will include comparison of blood inflammatory biomarkers, microbial translocation, blood and gut immunology and HIV levels, the bacterial community composition, diet, intestinal permeability, and the safety, adherence and tolerability of the study product.

Discussion: These studies will evaluate the ability of probiotics as a safe and tolerable therapeutic intervention to reduce systemic immune activation and to accelerate gut immune restoration in people living with HIV.

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来源期刊
HIV Clinical Trials
HIV Clinical Trials 医学-传染病学
CiteScore
1.76
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: HIV Clinical Trials is devoted exclusively to presenting information on the latest developments in HIV/AIDS clinical research. This journal enables readers to obtain the most up-to-date, innovative research from around the world.
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