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Modulation of Regulatory T-Cell Subsets in Very Long-Term Treated Aviremic HIV+ Patients and Untreated Viremic Patients

机译:长期治疗的非病毒性HIV +患者和未治疗的病毒血症患者的调节性T细胞亚群的调节

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摘要

Naïve, central- and effector-like memory regulatory T cells (Tregs) were evaluated in untreated and long-term antiretroviral-treated HIV+ patients that showed comparable CD4+ cell levels, while being, respectively, viremic and aviremic. In the untreated patients, the percentage of naïve-like Tregs was significantly increased to the detriment of central memory regulatory T cells. This redistribution of regulatory Treg subsets may contribute to explain the partially preserved CD4+ cell counts seen in these patients despite the ongoing viremia. On the contrary, in the long-term treated patients, the percentages of Treg subsets were similar to those of healthy donors, demonstrating a restored Treg homeostasis. The characterization of Treg subsets, rather than an evaluation of the total Treg population, may lead to a deeper understanding of the Treg role in HIV infection and therapy.
机译:对未经治疗和长期抗逆转录病毒治疗的HIV + 患者的CD4 + 细胞水平具有可比性的幼稚,中枢和效应样记忆调节性T细胞(Tregs)进行了评估,分别是病毒血症和非病毒血症。在未经治疗的患者中,幼稚样Treg的百分比显着增加,从而损害了中枢记忆调节性T细胞。调节性Treg亚群的这种重新分布可能有助于解释尽管存在病毒血症,但在这些患者中发现的部分保存的CD4 + 细胞计数。相反,在长期接受治疗的患者中,Treg亚群的百分比与健康供体的百分比相似,这表明Treg体内稳态得以恢复。 Treg子集的表征而不是对Treg总数的评估,可能会导致人们更深入地了解Treg在HIV感染和治疗中的作用。

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