Infectious Diseases and Immunity in Global Health Program, Research Institute of the McGill University Health Centre, Montréal, Quebec, Canada.
Division of Hematology, Department of Medicine, McGill University Health Centre, Montréal, Quebec, Canada.
BMJ Open. 2019 Apr 20;9(4):e028444. doi: 10.1136/bmjopen-2018-028444.
People living with HIV (PLWH) on antiretroviral therapy (ART) do not progress to AIDS. However, they still suffer from an increased risk of inflammation-associated complications. HIV persists in long-lived CD4+ T cells, which form the major viral reservoir. The persistence of this reservoir despite long-term ART is the major hurdle to curing HIV. Importantly, the size of the HIV reservoir is larger in individuals who start ART late in the course of infection and have a low CD4+/CD8+ ratio. HIV reservoir size is also linked to the levels of persistent inflammation on ART. Thus, novel strategies to reduce immune inflammation and improve the host response to control the HIV reservoir would be a valuable addition to current ART. Among the different strategies under investigation is metformin, a widely used antidiabetic drug that was recently shown to modulate T-cell activation and inflammation. Treatment of non-diabetic individuals with metformin controls inflammation by improving glucose metabolism and by regulating intracellular immunometabolic checkpoints such as the adenosin 5 monophosphate activated protein kinase and mammalian target of rapamycin, in association with microbiota modification.
22 PLWH on ART for more than 3 years, at high risk of inflammation or the development of non-AIDS events (low CD4+/CD8+ ratio) will be recruited in a clinical single-arm pilot study. We will test whether supplementing ART with metformin in non-diabetic HIV-infected individuals can reduce the size of the HIV reservoir as determined by various virological assays. The expected outcome of this study is a reduction in both the size of the HIV reservoir and inflammation following the addition of metformin to ART, thus paving the way towards HIV eradication.
Ethical approval: McGill university Health Centre committee number MP-37-2016-2456. Canadian Canadian Institutes of Health Research/Canadian HIV Trials Network (CTN) protocol CTNPT027. Results will be made available through publication in peer-reviewed journals and through the CTN website.
NCT02659306.
接受抗逆转录病毒疗法(ART)的艾滋病毒感染者(PLWH)不会发展为艾滋病。然而,他们仍然面临炎症相关并发症的风险增加。HIV 存在于长寿的 CD4+T 细胞中,这些细胞构成了主要的病毒储存库。尽管长期接受 ART 治疗,但这种储存库仍然存在,这是治愈 HIV 的主要障碍。重要的是,在感染过程中晚期开始 ART 且 CD4+/CD8+ 比值较低的个体中,HIV 储存库的大小更大。HIV 储存库的大小也与 ART 上持续存在的炎症水平有关。因此,减少免疫炎症并改善宿主对控制 HIV 储存库的反应的新策略将是当前 ART 的有价值的补充。在正在研究的不同策略中,二甲双胍是一种广泛使用的抗糖尿病药物,最近研究表明,它可以调节 T 细胞的激活和炎症。二甲双胍治疗非糖尿病患者可通过改善葡萄糖代谢以及通过调节细胞内免疫代谢检查点(如腺苷 5 单磷酸激活蛋白激酶和哺乳动物雷帕霉素靶蛋白)来控制炎症,同时还可调节微生物群。
将招募 22 名接受 ART 治疗超过 3 年的 PLWH,这些患者处于炎症高风险或发生非艾滋病事件(CD4+/CD8+ 比值低)的高风险中,这将是一项临床单臂试点研究。我们将测试在非糖尿病 HIV 感染者中,ART 中补充二甲双胍是否可以通过各种病毒学检测来减少 HIV 储存库的大小。这项研究的预期结果是,在 ART 中添加二甲双胍后,HIV 储存库的大小和炎症都会减少,从而为 HIV 根除铺平道路。
伦理批准:麦吉尔大学健康中心委员会编号 MP-37-2016-2456。加拿大加拿大卫生研究院/加拿大艾滋病毒临床试验网络(CTN)协议 CTNPT027。结果将通过在同行评议期刊上发表和 CTN 网站上发布。
NCT02659306。