Scheri Giuseppe Corano, Fard Saeid Najafi, Schietroma Ivan, Mastrangelo Andrea, Pinacchio Claudia, Giustini Noemi, Serafino Sara, De Girolamo Gabriella, Cavallari Eugenio Nelson, Statzu Maura, Laghi Luca, Vullo Annamaria, Ceccarelli Giancarlo, Vullo Vincenzo, d'Ettorre Gabriella
Department of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy.
Laboratory of Virology, Department of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Int J Tryptophan Res. 2017 May 30;10:1178646917710668. doi: 10.1177/1178646917710668. eCollection 2017.
To date, no data are available regarding the effects of probiotics on the pathway of tryptophan/serotonin metabolism among human immunodeficiency virus (HIV) 1-infected individuals. Because a condition of dysbiosis might be responsible for the altered use of tryptophan described in this population, the aim of this study was to investigate the link between probiotic supplementation and serotonin levels in combined antiretroviral therapy-treated patients and the subsistence of an interplay with inflammation.
We conducted a pilot study that included 8 HIV-positive subjects. We collected blood and fecal samples before and after 6 months of probiotic supplementation, to measure the level of serotonin in serum and tryptophan in stool, the expression of CD38 and HLA-DR on peripheral CD4+ T lymphocytes (as immune activation markers), the expression of indoleamine 2,3-dioxygenase 1 messenger RNA (mRNA) and IFN-γ mRNA (as markers of tryptophan metabolism and systemic inflammation).
After probiotic supplementation, we observed a significant increase in concentration of serum serotonin ( = .008) and a decreased level of tryptophan in plasma. Moreover, a significant reduction in CD38 and HLA-DR expression on the surface of peripheral CD4+ T cells ( = .008) and a reduced expression of indoleamine 2,3-dioxygenase 1 mRNA on peripheral blood mononuclear cells ( = .04) were observed.
Considering that this probiotic (Vivomixx® in EU; Visbiome® in USA) has an influence on tryptophan metabolism, larger studies on this topic are needed.
迄今为止,尚无关于益生菌对人类免疫缺陷病毒1型(HIV-1)感染者色氨酸/血清素代谢途径影响的数据。由于菌群失调可能是该人群中色氨酸使用改变的原因,本研究的目的是调查在接受联合抗逆转录病毒治疗的患者中补充益生菌与血清素水平之间的联系,以及与炎症相互作用的持续存在情况。
我们进行了一项试点研究,纳入了8名HIV阳性受试者。在补充益生菌6个月前后采集血液和粪便样本,以测量血清中血清素水平和粪便中色氨酸水平、外周CD4+T淋巴细胞上CD38和HLA-DR的表达(作为免疫激活标志物)、吲哚胺2,3-双加氧酶1信使核糖核酸(mRNA)和IFN-γmRNA的表达(作为色氨酸代谢和全身炎症的标志物)。
补充益生菌后,我们观察到血清血清素浓度显著升高(P = 0.008),血浆中色氨酸水平降低。此外,还观察到外周CD4+T细胞表面CD38和HLA-DR表达显著降低(P = 0.008),外周血单核细胞上吲哚胺2,3-双加氧酶1 mRNA表达降低(P = 0.04)。
鉴于这种益生菌(在欧盟为Vivomixx®;在美国为Visbiome®)对色氨酸代谢有影响,需要针对该主题开展更大规模的研究。