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Macrophage protection by addition of glutathione (GSH)-loaded erythrocytes to AZT and DDI in a murine AIDS model.

机译:在小鼠艾滋病模型中,通过向AZT和DDI中添加谷胱甘肽(GSH)加载的红细胞来保护巨噬细胞。

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Monocyte-macrophages play a central role in HIV-1 infection because they are among the first cells to be infected and because later they are important reservoirs for the virus. Thus, newly designed therapies should take into account the protection of this cell compartment. Herein, we report the results obtained in a murine AIDS model, by the addition to AZT+DDI of a system (GSH-loaded erythrocytes) able to protect macrophages against HIV-1 infection. Five groups of LP-BM5-infected mice were treated as follows: one group was treated by AZT, one group was treated by DDI, one group was treated by the combination of both, another by GSH-loaded erythrocytes, and finally, one by the combination of all three. After 10 weeks of infection the parameters of the disease were studied and the proviral DNA content in different organs and in macrophages of bone marrow and of the peritoneal cavity was quantified. The results obtained show that mice treated with AZT+DDI+GSH-loaded erythrocytes showed proviral DNA content in the brain and in macrophages of bone marrow that was significantly lower than in mice treated with AZT+DDI. This study may help developing strategies aimed at blocking HIV-1 replication in its reservoirs in the body.
机译:单核细胞巨噬细胞在HIV-1感染中起着核心作用,因为它们是最早被感染的细胞之一,并且因为后来它们是该病毒的重要储存库。因此,新设计的疗法应考虑对这种细胞室的保护。在这里,我们报告了在小鼠艾滋病模型中获得的结果,方法是将能够保护巨噬细胞免受HIV-1感染的系统(载有GSH的红细胞)添加到AZT + DDI中。五组被LP-BM5感染的小鼠的治疗方法如下:一组用AZT治疗,一组用DDI治疗,一组通过两者联合治疗,另一组通过GSH加载的红细胞治疗,最后一组这三者的结合。感染10周后,研究了疾病的参数,并定量了不同器官,骨髓和腹膜腔巨噬细胞中的前病毒DNA含量。获得的结果表明,用载有AZT + DDI + GSH的红细胞处理的小鼠的大脑和骨髓巨噬细胞中的前病毒DNA含量明显低于用AZT + DDI的小鼠。这项研究可能有助于制定旨在阻止HIV-1在其体内贮库中复制的策略。

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