Tan Darrell H S, Raboud Janet M, Szadkowski Leah, Yi Tae Joon, Shannon Brett, Kaul Rupert, Liles W Conrad, Walmsley Sharon L
1 Department of Medicine, University of Toronto , Toronto, Canada .
AIDS Res Hum Retroviruses. 2015 Mar;31(3):276-81. doi: 10.1089/AID.2014.0183. Epub 2014 Dec 17.
Systemic inflammation and immune activation may persist in HIV-infected persons on suppressive combination antiretroviral therapy (cART) and contribute to adverse health outcomes. We compared markers of immune activation, inflammation, and abnormal glucose and lipid metabolism in HIV-infected adults according to herpes simplex virus type 2 (HSV-2) serostatus in a 6-month observational cohort study in Toronto, Canada. HIV-infected adults on suppressive (viral load <50 copies/ml) cART were categorized as HSV-2 seropositive or seronegative using the HerpeSelect ELISA, and underwent study visits at baseline, 3 months, and 6 months. The primary outcome was the median percentage of activated (CD38(+)HLADR(+)) CD8 T cells. Secondary outcome measures included additional immune (activated CD4, regulatory T cells) and inflammatory (hsCRP, D-dimer, IL-1b, IL-6, MCP-1, TNF, sICAM-1, sVCAM-1, Ang1/Ang2 ratio) markers. Metabolic outcomes included the proportion with impaired fasting glucose/impaired glucose tolerance/diabetes, insulin sensitivity (calculated using the Matsuda index), insulin resistance (homeostasis model assessment of insulin resistance), and fasting lipids. The impact of HSV-2 on each outcome was estimated using generalized estimating equation regression models. Of 84 participants, 38 (45%) were HSV-2 seropositive. HSV signs and symptoms were uncommon. Aside from D-dimer, which was more often detectable in HSV-2 seropositives (adjusted odds ratio=3.58, 95% CI=1.27, 10.07), HSV-2 serostatus was not associated with differences in any other immune, inflammatory cytokine, acute phase reactant, endothelial activation, or metabolic markers examined in univariable or multivariable models. During the study, CD8 and CD4 T cell activation declined by 0.16% and 0.08% per month, respectively, while regulatory T cells increased by 0.05% per month. HSV-2 serostatus was not consistently associated with immune activation, inflammatory, or lipid and glucose metabolic markers in this cohort of HIV-infected adults on suppressive cART.
在接受抑制性联合抗逆转录病毒疗法(cART)的HIV感染者中,全身炎症和免疫激活可能持续存在,并导致不良健康后果。在加拿大多伦多进行的一项为期6个月的观察性队列研究中,我们根据2型单纯疱疹病毒(HSV-2)血清学状态,比较了HIV感染成人的免疫激活、炎症以及葡萄糖和脂质代谢异常的标志物。使用HerpeSelect ELISA将接受抑制性(病毒载量<50拷贝/ml)cART的HIV感染成人分为HSV-2血清阳性或血清阴性,并在基线、3个月和6个月时进行研究访视。主要结局是活化(CD38(+)HLADR(+))CD8 T细胞的中位数百分比。次要结局指标包括其他免疫(活化CD4、调节性T细胞)和炎症(hsCRP、D-二聚体、IL-1b、IL-6、MCP-1、TNF、sICAM-1、sVCAM-1、Ang1/Ang2比值)标志物。代谢结局包括空腹血糖受损/糖耐量受损/糖尿病的比例、胰岛素敏感性(使用松田指数计算)、胰岛素抵抗(胰岛素抵抗的稳态模型评估)和空腹血脂。使用广义估计方程回归模型估计HSV-2对每个结局的影响。在84名参与者中,38名(45%)为HSV-2血清阳性。HSV的体征和症状并不常见。除了D-二聚体在HSV-2血清阳性者中更常检测到(调整后的优势比=3.58,95%CI=1.27,10.07)外,在单变量或多变量模型中,HSV-2血清学状态与任何其他免疫、炎性细胞因子、急性期反应物、内皮激活或代谢标志物的差异均无关联。在研究期间,CD8和CD4 T细胞活化每月分别下降0.16%和0.08%,而调节性T细胞每月增加0.05%。在这一接受抑制性cART的HIV感染成人群体中,HSV-2血清学状态与免疫激活、炎症或脂质及葡萄糖代谢标志物之间并无一致关联。