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Innate immunity and chronic immune activation in HCV/HIV-1 co-infection.

机译:HCV / HIV-1共感染中的先天免疫和慢性免疫激活。

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摘要

Innate immune responses are critical in the defense against viral infections. NK cells, myeloid and plasmacytoid dendritic cells, and invariant CD1d-restricted NKT cells mediate both effector and regulatory functions in this early immune response. In chronic uncontrolled viral infections such as HCV and HIV-1, these essential immune functions are compromised and can become a double edged sword contributing to the immunopathogenesis of viral disease. In particular, recent findings indicate that innate immune responses play a central role in the chronic immune activation which is a primary driver of HIV-1 disease progression. HCV/HIV-1 co-infection is affecting millions of people and is associated with faster viral disease progression. Here, we review the role of innate immunity and chronic immune activation in HCV and HIV-1 infection, and discuss how mechanisms of innate immunity may influence protection as well as immunopathogenesis in the HCV/HIV-1 co-infected human host.
机译:先天性免疫反应在防御病毒感染中至关重要。 NK细胞,髓样细胞和浆细胞样树突状细胞以及不变的CD1d限制性NKT细胞在这种早期免疫反应中介导效应子和调节功能。在诸如HCV和HIV-1之类的慢性不受控制的病毒感染中,这些基本的免疫功能受到损害,并可能成为导致病毒性疾病免疫发病机理的双刃剑。特别是,最近的发现表明,先天免疫应答在慢性免疫激活中起着核心作用,而慢性免疫激活是HIV-1疾病进展的主要驱动力。 HCV / HIV-1合并感染正在影响数以百万计的人,并与更快的病毒性疾病进展有关。在这里,我们回顾了先天免疫和慢性免疫激活在HCV和HIV-1感染中的作用,并讨论了先天免疫的机制如何影响HCV / HIV-1共感染人类宿主的保护以及免疫发病机制。

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