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Cellular Compartments of Human Immunodeficiency Virus Type 1 Replication In Vivo: Determination by Presence of Virion-Associated Host Proteins and Impact of Opportunistic Infection

机译:人体免疫缺陷病毒1型体内复制的细胞隔间:病毒体相关宿主蛋白的存在和机会性感染的影响确定。

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摘要

Antigens derived from host cells are detectable in the envelope of human immunodeficiency virus type 1 (HIV-1) and result in a distinctive viral phenotype reflecting that of the host cell. An immunomagnetic capture assay targeting discriminatory host proteins was developed to differentiate between HIV-1 derived from macrophages and lymphocytes. HIV-1 propagated in macrophages or lymphocytes in vitro was selectively captured by monoclonal antibodies directed against the virally incorporated cell-type-specific host markers CD36 (macrophages) and CD26 (lymphocytes). Furthermore, by targeting these markers, virus of defined cellular origin was selectively captured from a mixed pool of in vitro-propagated viruses. This technique was further refined in order to determine the impact of opportunistic infection on HIV-1 expression from these cellular compartments in vivo. Analysis of cell-free virus purified from plasma of patients with HIV-1 infection suggested that in those with an opportunistic infection, viral replication occurred in activated lymphocytes. Interestingly, there was also significant replication in activated macrophages in those patients with untreated pulmonary tuberculosis. Thus, in addition to lymphocytes, the macrophage cellular pool may serve as an important source of cell-free HIV-1 in patients with opportunistic infections that lead to marked macrophage activation. This novel viral capture technique may allow researchers to address a wide range of important questions regarding virus-host dynamics.
机译:源自宿主细胞的抗原可在人免疫缺陷病毒1型(HIV-1)的包膜中检测到,并导致反映宿主细胞特征的独特病毒表型。开发了一种针对歧视性宿主蛋白的免疫磁捕获测定法,以区分源自巨噬细胞的HIV-1和淋巴细胞。通过针对病毒掺入的细胞类型特异性宿主标记CD36(巨噬细胞)和CD26(淋巴细胞)的单克隆抗体选择性捕获在体外在巨噬细胞或淋巴细胞中繁殖的HIV-1。此外,通过靶向这些标记,可以从混合的体外繁殖病毒库中选择性捕获具有明确细胞起源的病毒。为了确定机会性感染对体内这些细胞区室中HIV-1表达的影响,对该技术进行了进一步完善。从HIV-1感染患者血浆中纯化的无细胞病毒的分析表明,在机会感染患者中,活化的淋巴细胞中发生病毒复制。有趣的是,未经治疗的肺结核患者的活化巨噬细胞中也有大量复制。因此,除了淋巴细胞外,巨噬细胞池还可以作为机会性感染患者的重要无源HIV-1来源,导致机会性巨噬细胞活化。这种新颖的病毒捕获技术可以使研究人员解决有关病毒宿主动态的一系列重要问题。

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