BMC Infect Dis. 2013 Jun 4;13:263. doi: 10.1186/1471-2334-13-263.
HIV-1-related inflammation is associated with increased levels of biomarkers of vascular adhesion and endothelial activation, and may increase production of the inflammatory protein angiopoietin-2 (ANG-2), an adverse prognostic biomarker in severe systemic infection. We hypothesized that antiretroviral therapy (ART) initiation would decrease endothelial activation, reducing plasma levels of ANG-2.
Antiretroviral-naïve Kenyan women with advanced HIV infection were followed prospectively. Endothelial activation biomarkers including soluble intercellular adhesion molecule-1 (ICAM-1), vascular adhesion molecule-1 (VCAM-1), and E-selectin, and plasma ANG-2 and angiopoietin-1 (ANG-1) were tested in stored plasma samples from 0, 6, and 12 months after ART initiation. We used Wilcoxon matched-pairs signed rank tests to compare endothelial activation biomarkers across time-points, generalized estimating equations to analyze associations with change in log10-transformed biomarkers after ART initiation, and Cox proportional-hazards regression to analyze associations with mortality.
The 102 HIV-1-seropositive women studied had advanced infection (median CD4 count, 124 cells/μL). Soluble ICAM-1 and plasma ANG-2 levels decreased at both time-points after ART initiation, with concomitant increases in the beneficial protein ANG-1. Higher ANG-2 levels after ART initiation were associated with higher plasma HIV-1 RNA, oral contraceptive pill use, pregnancy, severe malnutrition, and tuberculosis. Baseline ANG-2 levels were higher among five women who died after ART initiation than among women who did not (median 2.85 ng/mL [inter-quartile range (IQR) 2.47-5.74 ng/mL] versus median 1.32 ng/mL [IQR 0.35-2.18 ng/mL], p = 0.01). Both soluble ICAM-1 and plasma ANG-2 levels predicted mortality after ART initiation.
Biomarkers of endothelial activation decreased after ART initiation in women with advanced HIV-1 infection. Changes in plasma ANG-2 were associated with HIV-1 RNA levels over 12 months of follow-up. Soluble ICAM-1 and plasma ANG-2 levels represent potential biomarkers for adverse outcomes in advanced HIV-1 infection.
HIV-1 相关炎症与血管黏附及内皮激活生物标志物水平升高有关,并且可能增加促炎蛋白血管生成素-2(ANG-2)的产生,ANG-2 是严重全身感染的不良预后生物标志物。我们假设抗逆转录病毒治疗(ART)的启动将降低内皮激活,从而降低血浆 ANG-2 水平。
前瞻性随访肯尼亚无抗逆转录病毒治疗史的晚期 HIV 感染女性。在 ART 启动后 0、6 和 12 个月,用存储的血浆样本检测内皮激活生物标志物,包括可溶性细胞间黏附分子-1(ICAM-1)、血管黏附分子-1(VCAM-1)和 E-选择素,以及血浆 ANG-2 和血管生成素-1(ANG-1)。我们使用 Wilcoxon 配对符号秩检验比较各时间点的内皮激活生物标志物,用广义估计方程分析 ART 启动后 log10 转化生物标志物变化的相关性,用 Cox 比例风险回归分析与死亡率的相关性。
102 例 HIV-1 阳性女性研究对象均为晚期感染(中位 CD4 计数 124 个/μL)。可溶性 ICAM-1 和 ANG-2 水平在 ART 启动后两个时间点均降低,同时有益蛋白 ANG-1 水平升高。ART 启动后 ANG-2 水平升高与血浆 HIV-1 RNA 较高、口服避孕药使用、妊娠、严重营养不良和结核病有关。在 ART 启动后死亡的 5 名女性的基线 ANG-2 水平高于未死亡的女性(中位数 2.85ng/ml [四分位距(IQR)2.47-5.74ng/ml]与中位数 1.32ng/ml [IQR 0.35-2.18ng/ml],p=0.01)。可溶性 ICAM-1 和 ANG-2 水平均预测 ART 启动后的死亡率。
晚期 HIV-1 感染女性在 ART 启动后内皮激活生物标志物降低。在 12 个月的随访中,血浆 ANG-2 的变化与 HIV-1 RNA 水平相关。可溶性 ICAM-1 和 ANG-2 水平可能是晚期 HIV-1 感染不良结局的潜在生物标志物。