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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

Na?ve, 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 na?ve-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:在未经治疗和长期接受抗逆转录病毒治疗的HIV +患者中评估了幼稚,中枢和效应子样记忆调节性T细胞(Tregs),这些患者表现出可比较的CD4 +细胞水平,而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Tregs的百分比显着增加,从而损害了中枢记忆调节性T细胞。尽管正在进行病毒血症,但调节性Treg亚群的这种重新分布可能有助于解释在这些患者中看到的部分保存的CD4 +细胞计数。相反,在长期接受治疗的患者中,Treg亚型的百分比与健康供体的百分比相似,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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