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慢性 HIV-1 感染患者中 CCR5 拮抗剂强化抗逆转录病毒治疗:对潜伏感染 T 细胞的影响。

Intensification of antiretroviral therapy with a CCR5 antagonist in patients with chronic HIV-1 infection: effect on T cells latently infected.

机构信息

Infectious Diseases Department, Hospital Universitario Ramón y Cajal, and IRYCIS, Madrid, Spain.

出版信息

PLoS One. 2011;6(12):e27864. doi: 10.1371/journal.pone.0027864. Epub 2011 Dec 8.

Abstract

OBJECTIVE

The primary objective was to assess the effect of MVC intensification on latently infected CD4(+) T cells in chronically HIV-1-infected patients receiving antiretroviral therapy.

METHODS

We performed an open-label pilot phase II clinical trial involving chronically HIV-1-infected patients receiving stable antiretroviral therapy whose regimen was intensified with 48 weeks of maraviroc therapy. We analyzed the latent reservoir, the residual viremia and episomal 2LTR DNA to examine the relationship between these measures and the HIV-1 latent reservoir, immune activation, lymphocyte subsets (including effector and central memory T cells), and markers associated with bacterial translocation.

RESULTS

Overall a non significant reduction in the size of the latent reservoir was found (p = 0.068). A mean reduction of 1.82 IUPM was observed in 4 patients with detectable latent reservoir at baseline after 48 weeks of intensification. No effect on plasma residual viremia was observed. Unexpectedly, all the patients had detectable 2LTR DNA circles at week 24, while none of them showed those circles at the end of the study. No changes were detected in CD4(+) or CD8(+) counts, although a significant decrease was found in the proportion of HLA-DR(+)/CD38(+) CD4(+) and CD8(+) T-cells. LPS and sCD14 levels increased.

CONCLUSIONS

Intensification with MVC was associated with a trend to a decrease in the size of the latent HIV-1 reservoir in memory T cells. No impact on residual viremia was detected. Additional studies with larger samples are needed to confirm the results.

TRIAL REGISTRATION

ClinicalTrials.gov NCT00795444.

摘要

目的

主要目的是评估在接受抗逆转录病毒治疗的慢性 HIV-1 感染患者中,强化 MVC 对潜伏感染的 CD4(+)T 细胞的影响。

方法

我们进行了一项开放性、Ⅱ期临床试验,纳入了接受稳定抗逆转录病毒治疗的慢性 HIV-1 感染患者,他们的治疗方案通过 48 周的马拉维若治疗得到强化。我们分析了潜伏储库、残留病毒血症和游离 2LTR DNA,以检查这些措施与 HIV-1 潜伏储库、免疫激活、淋巴细胞亚群(包括效应和中央记忆 T 细胞)以及与细菌易位相关的标志物之间的关系。

结果

总体而言,潜伏储库的大小没有明显减少(p=0.068)。在基线时有可检测潜伏储库的 4 名患者中,强化治疗 48 周后观察到潜伏储库平均减少 1.82 IUPM。未观察到对血浆残留病毒血症的影响。出乎意料的是,所有患者在第 24 周都检测到了可检测的 2LTR DNA 环,而在研究结束时没有一个患者显示出这些环。未检测到 CD4(+)或 CD8(+)计数的变化,尽管 HLA-DR(+)/CD38(+)CD4(+)和 CD8(+)T 细胞的比例明显下降。LPS 和 sCD14 水平增加。

结论

MVC 强化治疗与记忆 T 细胞中潜伏 HIV-1 储库大小减少的趋势相关。未检测到残留病毒血症的影响。需要更大样本量的进一步研究来证实结果。

试验注册

ClinicalTrials.gov NCT00795444。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/164f/3234247/91def9a69ee3/pone.0027864.g001.jpg

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