Netanya S Utay, Ana N Monczor, Anoma Somasunderam, Sofia Lupo, Zhi-Dong Jiang, Ashley S Alexander, Malcolm Finkelman, Karen J Vigil, Jordan E Lake, Blake Hanson, Herbert L DuPont, Roberto C Arduino
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引用次数: 7
Abstract
Background: Reduced microbiota diversity (dysbiosis) in people with HIV (PWH) likely contributes to inflammation, a driver of morbidity and mortality. We aimed to evaluate the safety and tolerability of 6 weekly oral fecal microbiota transplants (FMT) administered to reverse this dysbiosis.
Methods: Six PWH on suppressive antiretroviral therapy (ART) received 6 weekly doses of lyophilized fecal microbiota product from healthy donors. Shotgun sequencing on stool before, after last FMT, and 20 weeks thereafter was performed. Inflammation and gut permeability biomarkers were measured.
Results: Median age at week 0 was 39 years, CD4+ T cell count 496 cells/mm3, HIV RNA levels <20 copies/mL. FMT was safe and well-tolerated. α diversity increased in 4 participants from weeks 0 to 6, including the 3 with the lowest α diversity at week 0. At week 26, α diversity more closely resembled week 0 than week 6 in these 4 participants. Metagenomic analysis showed no consistent changes across all participants. One participant had high gut permeability and inflammation biomarker levels and low α diversity that improved between weeks 0 and 6 with a shift in distribution.
Conclusions: Weekly FMT was safe and well-tolerated. α diversity increased in participants with the lowest baseline α diversity during the treatment period. Future randomized, controlled trials of FMT should consider evaluating PWH with greater inflammation, gut damage, or dysbiosis as this population may be most likely to show a significant response.ClinicalTrials.gov Identifier: NCT03329560.
背景:HIV感染者(PWH)的微生物群多样性减少(生态失调)可能导致炎症,这是发病率和死亡率的驱动因素。我们的目的是评估每周6次的口服粪便微生物群移植(FMT)的安全性和耐受性,以逆转这种生态失调。方法:6名接受抗逆转录病毒抑制性治疗(ART)的PWH患者接受6周剂量的健康供体冻干粪便菌群产品。在最后一次FMT之前、之后和之后20周对粪便进行鸟枪测序。测量炎症和肠通透性生物标志物。结果:第0周的中位年龄为39岁,CD4+ T细胞计数496个细胞/mm3, HIV RNA水平。结论:每周FMT是安全且耐受性良好的。α多样性基线最低的受试者在治疗期间α多样性增加。未来的FMT随机对照试验应考虑评估有较大炎症、肠道损伤或生态失调的PWH,因为这类人群最有可能显示出显著的应答。