Department of Immunobiology, University of Arizona, Tucson, Arizona, USA.
Department of Medicine, College of Medicine, University of Arizona, Tucson, Arizona, USA.
Viral Immunol. 2024 May;37(4):202-215. doi: 10.1089/vim.2023.0123.
HIV-infected (HIV) aging adult individuals who have achieved undetectable viral load and improved CD4 T cell counts due to long-term antiretroviral therapy (ART) may continue to experience inflammation and immunosenescence. Therefore, we evaluated the plasma levels of proinflammatory and anti-inflammatory cytokines in 173 HIV aging adult individuals with age ranging from 22 to 81 years on long-term ART with viral load mostly <20 HIV RNA copies/mL and compared with 92 HIV-uninfected (HIV or healthy controls) aging individuals. We found that the median levels of TNF-α, IFN-γ, IL-1β, IL-6, and IL-10 were higher ( < 0.001 to <0.0001) and IL-17 trended lower in HIV individuals than healthy controls. Increasing CD4 T cell counts in the HIV cohort did not significantly change the circulating cytokine levels, although levels of IL-1β increased. However, IL-17 levels significantly decreased with increasing CD4 counts in the healthy controls and yet unchanged in the HIV cohort. Of note, the levels of circulating IL-17 were significantly reduced comparatively in the healthy controls where the CD4 count was below 500, yet once above 500 the levels of CD4, IL-17 levels were comparable with the HIV cohort. With increasing CD8 T cell counts, the levels of these cytokines were not significantly altered, although levels of TNF-α, IFN-γ, and IL-6 declined, whereas IL-1β and IL-17 were slightly elevated. Furthermore, increasing age of the HIV cohort did not significantly impact the cytokine levels although a slight increase in TNF-α, IL-6, IL-10, and IL-17 was observed. Similarly, these cytokines were not significantly modulated with increasing levels of undetectable viral loads, whereas some of the HIV individuals had higher levels of TNF-α, IFN-γ, and IL-1β. In summary, our findings show that HIV aging adult individuals with undetectable viral load and restored CD4 T cell counts due to long-term ART still produce higher levels of both proinflammatory and anti-inflammatory cytokines compared with healthy controls, suggesting some level of inflammation.
由于长期抗逆转录病毒治疗(ART),HIV 感染(HIV)的成年个体的病毒载量已无法检测到,CD4 T 细胞计数也有所提高,这些个体可能仍会经历炎症和免疫衰老。因此,我们评估了 173 名长期接受 ART 治疗、病毒载量大多<20 HIV RNA 拷贝/ml 的 HIV 成年个体的血浆中促炎和抗炎细胞因子的水平,并将其与 92 名未感染 HIV(HIV 或健康对照)的成年个体进行了比较。我们发现,与健康对照组相比,HIV 个体的 TNF-α、IFN-γ、IL-1β、IL-6 和 IL-10 的中位数水平更高(<0.001 至 <0.0001),而 IL-17 则呈下降趋势。尽管 CD4 T 细胞计数增加,但 HIV 组的循环细胞因子水平并没有显著改变,尽管 IL-1β 水平有所增加。然而,IL-17 水平在健康对照组中随着 CD4 计数的增加而显著降低,但在 HIV 组中则保持不变。值得注意的是,在 CD4 计数<500 的健康对照组中,循环 IL-17 的水平明显降低,但一旦超过 500,CD4 和 IL-17 的水平与 HIV 组相当。随着 CD8 T 细胞计数的增加,这些细胞因子的水平没有显著改变,尽管 TNF-α、IFN-γ 和 IL-6 的水平下降,而 IL-1β 和 IL-17 的水平略有升高。此外,随着 HIV 组年龄的增加,细胞因子水平没有显著变化,尽管 TNF-α、IL-6、IL-10 和 IL-17 的水平略有增加。同样,这些细胞因子也没有随着无法检测到的病毒载量的增加而显著调节,尽管一些 HIV 个体的 TNF-α、IFN-γ 和 IL-1β 水平较高。综上所述,我们的研究结果表明,由于长期抗逆转录病毒治疗,HIV 感染的成年个体的病毒载量已无法检测到,CD4 T 细胞计数也有所恢复,与健康对照组相比,这些个体仍会产生更高水平的促炎和抗炎细胞因子,这表明存在一定程度的炎症。