Guangxi Key Laboratory of AIDS Prevention and Treatment & Guangxi Universities Key Laboratory of Prevention and Control of Highly Prevalent Disease, School of Public Health, Guangxi Medical University, Nanning 530021, Guangxi, China.
Guangxi Key Laboratory of AIDS Prevention and Treatment & Guangxi Universities Key Laboratory of Prevention and Control of Highly Prevalent Disease, School of Public Health, Guangxi Medical University, Nanning 530021, Guangxi, China.
Drug Alcohol Depend. 2016 Feb 1;159:246-54. doi: 10.1016/j.drugalcdep.2015.12.027. Epub 2016 Jan 4.
Although a number of in vitro studies have shown that methamphetamine (METH) can increase HIV-1 replication in human immune cells, a direct link between METH use and HIV-1 pathogenesis remains to be determined among HIV-1 patients.
According to the status of METH use and HIV-1 infection, we enrolled participants and divided them into four groups: METH+HIV+, METH-HIV+, METH+HIV-, and METH-HIV-. HIV viral loads and HIV-1-related cellular factors were measured and compared among different groups.
A total of 60 participants were enrolled into this study, 15 within each group. HIV viral loads in METH+HIV+ group were significantly higher than those in METH-HIV+ group, while CD4+ T cell counts had an inverse trend between the two groups (p<0.05). METH users or HIV-1 infected patients had lower CCR5+, CXCR4+ percentages in CD4+ T cells than METH-HIV- subjects (p<0.01). However, METH use had little effect on CD3 expression in PBMCs and the levels of MIP-1α, MIP-1β and IL-6 in PBMCs or plasma, which were increased by HIV-1 infection with or without METH. TLR-9 and IFN-α levels in PBMCs of METH users with or without HIV infection were higher than non-METH users (p<0.05).
METH use is associated with higher viral loads and lower CD4+ T cell counts in HIV-infected individuals. This finding may be mediated by activation of innate immunity (TLR-9, IFN-α) by METH use.
尽管许多体外研究表明,甲基苯丙胺(METH)可以增加人类免疫细胞中的 HIV-1 复制,但在 HIV-1 患者中,METH 使用与 HIV-1 发病机制之间的直接联系仍有待确定。
根据 METH 使用和 HIV-1 感染的状况,我们招募了参与者并将他们分为四组:METH+HIV+、METH-HIV+、METH+HIV-和 METH-HIV-。测量并比较了不同组之间的 HIV 病毒载量和与 HIV-1 相关的细胞因子。
这项研究共招募了 60 名参与者,每组 15 名。METH+HIV+组的 HIV 病毒载量明显高于 METH-HIV+组,而两组之间的 CD4+T 细胞计数呈相反趋势(p<0.05)。METH 使用者或 HIV-1 感染者的 CD4+T 细胞中 CCR5+、CXCR4+的百分比低于 METH-HIV-受试者(p<0.01)。然而,METH 使用对 PBMC 中的 CD3 表达以及 PBMC 或血浆中 MIP-1α、MIP-1β 和 IL-6 的水平几乎没有影响,这些水平是由 HIV-1 感染引起的,无论是否使用 METH。无论是否感染 HIV,METH 使用者的 PBMC 中的 TLR-9 和 IFN-α水平均高于非 METH 使用者(p<0.05)。
METH 使用与 HIV 感染者中更高的病毒载量和更低的 CD4+T 细胞计数有关。这一发现可能是由 METH 使用激活先天免疫(TLR-9、IFN-α)介导的。