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利用定量竞争性逆转录聚合酶链反应对猫免疫缺陷病毒在血浆中的动力学进行纵向评估。

Longitudinal assessment of feline immunodeficiency virus kinetics in plasma by use of a quantitative competitive reverse transcriptase PCR.

作者信息

Diehl L J, Mathiason-DuBard C K, O'Neil L L, Hoover E A

机构信息

Department of Pathology, Colorado State University, Fort Collins 80523.

出版信息

J Virol. 1995 Apr;69(4):2328-32. doi: 10.1128/JVI.69.4.2328-2332.1995.

Abstract

Cats infected with feline immunodeficiency virus (FIV) develop a disease syndrome similar to that caused by human immunodeficiency virus type 1 (HIV-1) infection in humans. HIV-1 replication has been shown to correlate with the disease stage and progression. To assess replication kinetics and disease progression in early FIV infection, we developed a quantitative competitive reverse transcriptase PCR to measure the plasma virus load at serial time points after virus exposure. We found that an early peak viremia immediately preceded the onset of acute-phase symptoms in infected cats. Plasma virus levels remained high throughout the symptomatic phase of infection, which lasted for 8 to 10 weeks, and then declined as clinical symptoms resolved; however, all cats maintained significant plasma virus titers through 36 weeks postinfection. Early peak viral replication coincided with the initial precipitous decline in circulating CD4+ T lymphocytes. These results indicate that FIV kinetics are similar to those of HIV-1 during the acute and secondary phase of infection and that the plasma FIV load correlates with the disease stage. These results serve to further develop the FIV model and to enhance its usefulness for pathogenesis, vaccine development, and therapeutic studies related to HIV.

摘要

感染猫免疫缺陷病毒(FIV)的猫会出现一种疾病综合征,类似于人类感染1型人类免疫缺陷病毒(HIV-1)所引发的疾病综合征。已证明HIV-1复制与疾病阶段和进展相关。为了评估FIV早期感染中的复制动力学和疾病进展,我们开发了一种定量竞争性逆转录酶PCR,用于测量病毒暴露后连续时间点的血浆病毒载量。我们发现,早期病毒血症峰值紧接在受感染猫急性期症状出现之前。在持续8至10周的感染症状期,血浆病毒水平一直很高,然后随着临床症状的缓解而下降;然而,所有猫在感染后36周内血浆病毒滴度仍维持在显著水平。早期病毒复制峰值与循环CD4+T淋巴细胞最初的急剧下降同时出现。这些结果表明,在感染的急性期和二期,FIV的动力学与HIV-1相似,且血浆FIV载量与疾病阶段相关。这些结果有助于进一步发展FIV模型,并提高其在与HIV相关的发病机制、疫苗开发和治疗研究中的有用性。

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