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Induction of HIV Type 1 Expression Correlates with T Cell Responsiveness to Mycobacteria in Patients Coinfected with HIV Type 1 and Mycobacterium tuberculosis

机译:HIV 1型表达与结核分枝杆菌合并感染的患者中,HIV 1型表达的诱导与T细胞对分枝杆菌的反应性相关

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摘要

An in vitro mononuclear cell system to model the microenvironment of coinfection with HIV-1 and Mycobacterium tuberculosis (MTB) was developed. This cellular system was used to assess the interaction of MTB-infected monocytes and T cells from dually infected HIV-1/TB patients with pulmonary tuberculosis (TB). Subjects with higher induction of HIV-1gag/pol mRNA expression after MTB stimulation had increased MTB-specific T cell IFN-γ and TNF-α production. Lack of HIV-1 mRNA induction did not correlate with increased induction of regulatory T cells (T-reg) as measured by MTB-induced Foxp3 mRNA. HIV-1 induction did not significantly correlate with clinical parameters including plasma HIV-1 viral load or CD4+ T cell count. These data model MTB-induced HIV-1 replication at the microenvironment of MTB reactivation/infection. The data suggest that the magnitude of MTB-specific T cell responses drives local viral pathogenesis regardless of the stage of HIV-1 disease as reflected by plasma viral load or CD4+ T cell count.
机译:开发了体外单核细胞系统,以模拟与HIV-1和结核分枝杆菌(MTB)共同感染的微环境。该细胞系统用于评估双重感染的HIV-1 / TB患者合并肺结核(TB)的MTB感染的单核细胞和T细胞的相互作用。 MTB刺激后具有较高HIV-1gag / pol mRNA表达诱导能力的受试者的MTB特异性T细胞IFN-γ和TNF-α产生增加。通过MTB诱导的Foxp3 mRNA的测量,缺乏HIV-1 mRNA的诱导与调节性T细胞(T-reg)的诱导增加无关。 HIV-1的诱导与血浆HIV-1病毒载量或CD4 + T细胞计数等临床指标无显着相关性。这些数据在MTB激活/感染的微环境中模拟了MTB诱导的HIV-1复制。数据表明,不论血浆病毒载量或CD4 + T细胞计数如何,MTB特异性T细胞反应的强度都可驱动局部病毒发病机制,而与HIV-1疾病的阶段无关。

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  • 来源
    《AIDS Research and Human Retroviruses》 |2009年第2期|213-216|共4页
  • 作者单位

    Division of Infectious Diseases, Cleveland VA Hospital, Cleveland, Ohio 44106.;

    Division of Infectious Diseases, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106.;

    Division of Infectious Diseases, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106.;

    Division of Infectious Diseases, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106.;

    Department of Medicine, Joint Clinical Research Centre, Makerere University, Kampala, Uganda.;

    Department of Medicine, Joint Clinical Research Centre, Makerere University, Kampala, Uganda.;

    Division of Infectious Diseases, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106.;

    Department of Medicine, Joint Clinical Research Centre, Makerere University, Kampala, Uganda.;

    Division of Infectious Diseases, Cleveland VA Hospital, Cleveland, Ohio 44106.;

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