Maria Love, Nicole Behrens-Bradley, Aasim Ahmad, Anne Wertheimer, Stephen Klotz, Nafees Ahmad
{"title":"长期接受抗逆转录病毒疗法、病毒已得到控制的成年 HIV 感染者血浆中分泌的细胞因子水平。","authors":"Maria Love, Nicole Behrens-Bradley, Aasim Ahmad, Anne Wertheimer, Stephen Klotz, Nafees Ahmad","doi":"10.1089/vim.2023.0123","DOIUrl":null,"url":null,"abstract":"<p><p>HIV-infected (HIV<sup>+</sup>) 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<sup>+</sup> 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<sup>-</sup> 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 (<i>p</i> < 0.001 to <0.0001) and IL-17 trended lower in HIV<sup>+</sup> individuals than healthy controls. Increasing CD4 T cell counts in the HIV<sup>+</sup> 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<sup>+</sup> 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<sup>+</sup> 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<sup>+</sup> 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<sup>+</sup> individuals had higher levels of TNF-α, IFN-γ, and IL-1β. 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Therefore, we evaluated the plasma levels of proinflammatory and anti-inflammatory cytokines in 173 HIV<sup>+</sup> 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<sup>-</sup> 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 (<i>p</i> < 0.001 to <0.0001) and IL-17 trended lower in HIV<sup>+</sup> individuals than healthy controls. Increasing CD4 T cell counts in the HIV<sup>+</sup> 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<sup>+</sup> 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<sup>+</sup> 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<sup>+</sup> 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<sup>+</sup> individuals had higher levels of TNF-α, IFN-γ, and IL-1β. 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引用次数: 0
摘要
通过长期抗逆转录病毒疗法(ART)检测不到病毒载量并提高了 CD4 T 细胞计数的艾滋病病毒感染者(HIV+)老年成人可能会继续经历炎症和免疫衰老。因此,我们评估了 173 名年龄在 22 至 81 岁之间、长期接受抗逆转录病毒疗法且病毒载量大部分为健康对照组的 HIV 感染者(或健康对照组)的血浆促炎和抗炎细胞因子水平。我们发现,TNF-α、IFN-γ、IL-1β、IL-6 和 IL-10 的中位水平高于健康对照组(p +)。艾滋病病毒感染者中 CD4 T 细胞数量的增加并没有显著改变循环细胞因子的水平,但 IL-1β 的水平有所增加。然而,在健康对照组中,随着 CD4 细胞数量的增加,IL-17 的水平明显下降,而在艾滋病病毒感染者队列中却没有变化。值得注意的是,在 CD4 细胞计数低于 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、IL-17 的水平就与 HIV+ 组群相当。虽然 TNF-α、IFN-γ 和 IL-6 的水平有所下降,但随着 CD8 T 细胞数量的增加,这些细胞因子的水平并无明显变化,而 IL-1β 和 IL-17 则略有升高。此外,虽然 TNF-α、IL-6、IL-10 和 IL-17 的水平略有上升,但 HIV 感染者年龄的增加对细胞因子水平并无明显影响。同样,随着检测不到病毒载量水平的增加,这些细胞因子也没有明显变化,而一些艾滋病毒携带者的 TNF-α、IFN-γ 和 IL-1β 水平较高。总之,我们的研究结果表明,与健康对照组相比,病毒载量检测不到、CD4 T 细胞数量因长期抗逆转录病毒疗法而恢复的 HIV+ 老年成人仍会产生较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。
Plasma Levels of Secreted Cytokines in Virologically Controlled HIV-Infected Aging Adult Individuals on Long-Term Antiretroviral Therapy.
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 (p < 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.
期刊介绍:
Viral Immunology delivers cutting-edge peer-reviewed research on rare, emerging, and under-studied viruses, with special focus on analyzing mutual relationships between external viruses and internal immunity. Original research, reviews, and commentaries on relevant viruses are presented in clinical, translational, and basic science articles for researchers in multiple disciplines.
Viral Immunology coverage includes:
Human and animal viral immunology
Research and development of viral vaccines, including field trials
Immunological characterization of viral components
Virus-based immunological diseases, including autoimmune syndromes
Pathogenic mechanisms
Viral diagnostics
Tumor and cancer immunology with virus as the primary factor
Viral immunology methods.