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Note: Rapid CD4+ T-Cell Loss Induced by Human Immunodeficiency Virus Type 1NC in Uninfected and Previously Infected Chimpanzees

机译:注意:人类免疫缺陷病毒1NC型在未感染和先前感染的黑猩猩中引起的CD4 + T细胞快速丢失。

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摘要

To investigate the pathogenicity of a virus originating in a chimpanzee with AIDS (C499), two chimpanzees were inoculated with a plasma-derived isolate termed human immunodeficiency virus type 1NC (HIV-1NC). A previously uninfected chimpanzee, C534, experienced rapid peripheral CD4+ T-cell loss to fewer than 26 cells/μl by 14 weeks after infection. CD4+ T-cell depletion was associated with high plasma HIV-1 loads but a low virus burden in the peripheral lymph node. The second chimpanzee, C459, infected 13 years previously with HIV-1LAV, experienced a more protracted course of peripheral CD4+ T-cell loss after HIV-1NC inoculation, resulting in fewer than 200 cells/μl by 96 weeks postinoculation. The quantities of viral RNA in the plasma and peripheral lymph node from C459 were below the lower limits of detection prior to inoculation with HIV-1NC but were significantly and persistently increased after superinfection, with HIV-1NC representing the predominant viral genotype. These results show that viruses derived from C499 are more pathogenic for chimpanzees than any other HIV-1 isolates described to date.
机译:为了调查源自黑猩猩的艾滋病(C499)的病毒的致病性,用称为人免疫缺陷病毒1NC型(HIV-1NC)的血浆分离株接种了两只黑猩猩。以前未感染的黑猩猩C534在感染后14周时迅速出现外周CD4 + T细胞损失,少于26个细胞/μl。 CD4 + T细胞耗竭与血浆HIV-1负荷高但外周淋巴结病毒负荷低有关。在13年前感染HIV-1LAV的第二只黑猩猩C459,在HIV-1NC接种后,外周CD4 + T细胞丢失的过程更加漫长,导致少于200个细胞/μl。接种后96周。来自C459的血浆和外周淋巴结中的病毒RNA量低于接种HIV-1NC之前的检测下限,但在重复感染后显着且持续增加,其中HIV-1NC代表了主要的病毒基因型。这些结果表明,与迄今为止描述的任何其他HIV-1分离株相比,源自C499的病毒对黑猩猩的致病性更高。

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