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CD8+ lymphocyte phenotype and cytokine production in long-term non-progressor and in progressor patients with HIV-1 infection

机译:长期非进行性和进行性HIV-1感染患者的CD8 +淋巴细胞表型和细胞因子产生

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摘要

In most HIV-1-infected patients, clinical and immunological progression develops within a few years. Few infected people, termed long-term non-progressors (LTNP), remain healthy and immunologically stable for a long time. The factors governing the maintenance of this condition are not well known, but it is conceivable that CD8+ lymphocytes, cells that play a central role in controlling in vitro HIV replication, may have a part in vivo in this process. The aim of this study was to characterize the phenotypic profile and the cytokine production of CD8+ cells in a group of LTNP patients who had stable CD4+ cell counts (>500/mm3) for at least 7 years. Their CD8+ absolute numbers were similar to a control group composed of HIV-1+ patients who have a progressive decline of their CD4+ cell counts. However, our multiparameter immunofluorescence studies show that a clinical and immunologically stable condition is associated with the presence of a CD28+, CD95 strongly positive CD8+ population, while disease progression is marked by the CD28−CD95+CD8+ subset. Purified CD8+ cells from LTNP retain their ability to produce IL-2, interferon-gamma (IFN-γ) and, to a lesser degree, to produce IL-10 and IL-4. In contrast, CD8+ cells from progressors are unable to secrete IL-2 and IL-10. Although CD8+ cytokine profile does not fit with the proposed T helper (Th)1/Th2 switch in progressive HIV infection, LTNP CD8+ T cells maintain their capacity to produce IL-2 and IL-10 (Th0-like), a pattern very similar to that observed in normal HIV healthy controls. We suggest that CD8+ cells expressing CD28, CD95 and having a Th0-like profile may be considered to be associated with long-term survival.
机译:在大多数感染HIV-1的患者中,临床和免疫学进展会在几年内发展。很少有人被称为长期非进展者(LTNP),他们可以长期保持健康和免疫稳定。控制这种状况维持的因素尚不清楚,但是可以想象,CD8 +淋巴细胞是在控制体外HIV复制中起关键作用的细胞,在此过程中可能在体内起作用。这项研究的目的是表征一组CD7 +细胞计数稳定(> 500 / mm3)至少7年的LTNP患者的CD8 +细胞的表型和细胞因子产生。他们的CD8 +绝对数量类似于由HIV-1 +患者组成的对照组,这些患者的CD4 +细胞计数逐渐下降。然而,我们的多参数免疫荧光研究表明,临床和免疫学上稳定的疾病与CD28 +,CD95强阳性CD8 +群体的存在有关,而疾病进展以CD28-CD95 + CD8 +子集为标志。来自LTNP的纯化CD8 +细胞保留了产生IL-2,干扰素-γ(IFN-γ)的能力,并在较小程度上产生IL-10和IL-4的能力。相反,来自进展者的CD8 +细胞不能分泌IL-2和IL-10。尽管CD8 +细胞因子谱与进行性HIV感染中建议的T辅助(Th)1 / Th2开关不匹配,但LTNP CD8 + T细胞仍保持其产生IL-2和IL-10(Th0样)的能力,这种模式非常相似与正常HIV健康对照中观察到的情况相比。我们建议表达CD28,CD95并具有Th0样特征的CD8 +细胞可能被认为与长期生存有关。

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