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首页> 外文期刊>Journal of Venomous Animals and Toxins including Tropical Diseases >Assessment of cytokine values in serum by RT-PCR in HIV-1 infected individuals with and without highly active anti-retroviral therapy (HAART)
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Assessment of cytokine values in serum by RT-PCR in HIV-1 infected individuals with and without highly active anti-retroviral therapy (HAART)

机译:通过RT-PCR对有或没有高活性抗逆转录病毒疗法(HAART)的HIV-1感染者的血清中细胞因子值的评估

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摘要

A cross-sectional study was performed on HIV-1 infected individuals with or without antiretroviral treatment (ARV) in the AIDS Day Hospital, Botucatu Medical School, UNESP. Between August 2004 and October 2005, 73 HIV-1 infected individuals were divided into three groups: infected individuals with or without AIDS who had never received ARV (G1 = 15); patients on HAART that had had plasma HIV-1 RNA viral load (VL) equal to or greater than 50 copies/mL (G2 = 27); and patients on HAART with undetectable VL for at least the past six months (G3 = 31). There was also an additional group that comprised blood donors without any sign of the disease and with negative HIV serum tests (G4 = 20), which was the control group. Serum cytokine levels (values in pg/mL) were measured by enzyme-linked immunosorbent assay (ELISA) and specific mRNA expression by reverse transcription polymerase chain reaction (RT-PCR). Both techniques were performed on the four groups for TNF-α, IL-2, INF-γ, IL-4 and IL-10. All patients were submitted to VL determination and CD4+ and CD8+T lymphocyte counts. The analysis of the results revealed a significant comparison among groups for both methods and an association between the latter (> 80% r2 > 0.80). There was only one exception, in control individuals for IL-2 by ELISA. The cytokine profiles, in both methods, for the three patient groups, were mature Th-0. The behaviors of IL-2 and INF-γ required emphasis due to consequent expression of dominant Th profile. Both methods showed low IL-2 and high mean values of INF-γ in the three groups. Several authors have recently drawn attention to the substantial apoptosis of infected and non-infected CD4+T cells, mainly during primary infection, persisting only in those with INF-γ phenotype producer and not IL-2. HIV infected individuals submitted to HAART are expected to produce IL-2 in an attempt to present Th-1 profile, but in most cases this did not occur.
机译:在UNESP的Botucatu医学院艾滋病日医院,对接受或未接受抗逆转录病毒治疗(ARV)的HIV-1感染者进行了横断面研究。在2004年8月至2005年10月之间,将73名受HIV-1感染的人分为三类:从未接受过抗逆转录病毒治疗(G1 = 15)的有或没有AIDS的感染者; HAART患者血浆HIV-1 RNA病毒载量(VL)等于或大于50拷贝/ mL(G2 = 27);至少在过去六个月中,HAART患者的VL无法检测到(G3 = 31)。另外还有一个对照组,该组包括没有任何疾病迹象且HIV血清检测阴性的献血者(G4 = 20),这是对照组。血清细胞因子水平(以pg / mL为单位)通过酶联免疫吸附测定(ELISA)进行测定,特异性mRNA表达通过逆转录聚合酶链反应(RT-PCR)进行测定。两种技术均针对TNF-α,IL-2,INF-γ,IL-4和IL-10的四组进行。所有患者均接受VL测定以及CD4 +和CD8 + T淋巴细胞计数。结果分析表明,这两种方法的组之间存在显着比较,后者之间的关联性更高(> 80%r2> 0.80)。通过ELISA在对照个体中IL-2只有一个例外。在这两种方法中,三个患者组的细胞因子谱均为成熟的Th-0。由于占主导地位的Th谱的表达,需要强调IL-2和INF-γ的行为。两种方法在三组中均显示出低的IL-2和高的INF-γ平均值。最近有几位作者引起了人们对感染和未感染的CD4 + T细胞大量凋亡的关注,主要是在原发感染期间,仅在具有INF-γ表型产生者的细胞中持续存在,而在IL-2中却没有。提交HAART的被HIV感染的个体有望产生IL-2,以呈现Th-1谱,但在大多数情况下并未发生。

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