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Immunobiology: The level of monocyte turnover predicts disease progression in the macaque model of AIDS

机译:免疫生物学:单核细胞更新的水平可预测AIDS猕猴模型中的疾病进展

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摘要

It is widely accepted that destruction of CD4+ T cells and viral load are the primary markers for immunodeficiency in HIV-1–infected humans and in simian immunodeficiency virus (SIV)–infected macaques. However, monocyte/macrophages are also important targets of HIV/SIV infection and a critical link between innate and adaptive immunity. We therefore examined whether changes in cells of the monocyte/macrophage lineage could be linked to the pathogenesis of AIDS in the rhesus macaque model. Here, we show that massive turnover of peripheral monocytes associated with death of tissue macrophages correlates with AIDS progression in macaques. More importantly, the level of monocyte turnover was not linked to the CD4+ T-cell count and was a better predictive marker for AIDS progression than was viral load or lymphocyte activation. Our results show the importance of monocyte/macrophages in the pathogenesis of AIDS and suggest the dynamic changes of the monocyte/macrophages as a new marker for AIDS progression.
机译:人们普遍认为,CD4 + T细胞的破坏和病毒载量是感染HIV-1的人类和猿猴免疫缺陷病毒(SIV)感染的猕猴免疫缺陷的主要标志。但是,单核细胞/巨噬细胞也是HIV / SIV感染的重要目标,也是先天免疫和适应性免疫之间的关键纽带。因此,我们检查了猕猴模型中单核细胞/巨噬细胞谱系细胞的变化是否与艾滋病的发病机制有关。在这里,我们显示与巨噬细胞死亡相关的周围单核细胞的大量周转与猕猴的AIDS进展相关。更重要的是,单核细胞更新的水平与CD4 + T细胞计数无关,并且比病毒负荷或淋巴细胞活化更好地预测了AIDS的进展。我们的结果表明单核细胞/巨噬细胞在艾滋病发病机理中的重要性,并提示单核细胞/巨噬细胞的动态变化是艾滋病发展的新标志。

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