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Rapid clearance of simian immunodeficiency virus particles from plasma of rhesus macaques.恒河猴血浆中猿猴免疫缺陷病毒颗粒的快速清除。
J Virol. 1999 Jan;73(1):855-60. doi: 10.1128/JVI.73.1.855-860.1999.
2
The liver is a major organ for clearing simian immunodeficiency virus in rhesus monkeys.肝脏是恒河猴清除猴免疫缺陷病毒的主要器官。
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Current estimates for HIV-1 production imply rapid viral clearance in lymphoid tissues.目前对 HIV-1 产生的估计表明,在淋巴组织中病毒迅速清除。
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Short-Term Pegylated Interferon α2a Treatment Does Not Significantly Reduce the Viral Reservoir of Simian Immunodeficiency Virus-Infected, Antiretroviral Therapy-Treated Rhesus Macaques.短期聚乙二醇干扰素 α2a 治疗并不显著降低感染猴免疫缺陷病毒、接受抗逆转录病毒治疗的恒河猴的病毒储存库。
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Brain Macrophages in Simian Immunodeficiency Virus-Infected, Antiretroviral-Suppressed Macaques: a Functional Latent Reservoir.感染猿猴免疫缺陷病毒且接受抗逆转录病毒治疗抑制的猕猴中的脑巨噬细胞:一个功能性潜伏库
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Route of simian immunodeficiency virus inoculation determines the complexity but not the identity of viral variant populations that infect rhesus macaques.猿猴免疫缺陷病毒的接种途径决定了感染恒河猴的病毒变异群体的复杂性,但不决定其特性。
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Antibody-Mediated CD4 Depletion Induces Homeostatic CD4 T Cell Proliferation without Detectable Virus Reactivation in Antiretroviral Therapy-Treated Simian Immunodeficiency Virus-Infected Macaques.抗体介导的 CD4 耗竭在抗逆转录病毒治疗的感染猴免疫缺陷病毒的猕猴中诱导稳态 CD4 T 细胞增殖而不检测到病毒激活。
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本文引用的文献

1
The response of mice to large intravenous injections of ectromelia virus. II. The growth of virus in the liver.小鼠对大剂量静脉注射埃可病毒的反应。II. 病毒在肝脏中的生长
Br J Exp Pathol. 1959 Dec;40(6):543-50.
2
The response of mice to large intravenous injections of ectromelia virus. I. The fate of injected virus.小鼠对大剂量静脉注射埃可病毒的反应。I. 注射病毒的归宿
Br J Exp Pathol. 1959 Dec;40(6):533-42.
3
RELATIONSHIP BETWEEN BLOOD CLEARANCE AND VIRURIA AFTER INTRAVENOUS INJECTION OF MICE AND RATS WITH BACTERIOPHAGE AND POLIOVIRUSES.
J Immunol. 1965 Jun;94:833-41.
4
Blood clearance of P32-labeled vesicular stomatitis and Newcastle disease viruses by the reticuloendothelial system in mice.小鼠网状内皮系统对P32标记的水泡性口炎病毒和新城疫病毒的血液清除情况。
J Immunol. 1960 Jul;85:99-105.
5
Rift Valley Fever virus in mice. II. Adsorption and multiplication of virus.裂谷热病毒在小鼠体内的研究。II. 病毒的吸附与增殖
Br J Exp Pathol. 1956 Apr;37(2):110-9.
6
Dynamics of HIV-1 and CD4+ lymphocytes in vivo.体内HIV-1与CD4+淋巴细胞的动态变化
AIDS. 1997;11 Suppl A:S17-24.
7
Kinetics of CD4+ T cell repopulation of lymphoid tissues after treatment of HIV-1 infection.HIV-1感染治疗后淋巴组织中CD4+ T细胞再增殖的动力学
Proc Natl Acad Sci U S A. 1998 Feb 3;95(3):1154-9. doi: 10.1073/pnas.95.3.1154.
8
Viral dynamics of primary viremia and antiretroviral therapy in simian immunodeficiency virus infection.猿猴免疫缺陷病毒感染中初次病毒血症的病毒动力学及抗逆转录病毒疗法
J Virol. 1997 Oct;71(10):7518-25. doi: 10.1128/JVI.71.10.7518-7525.1997.
9
Perspectives series: host/pathogen interactions. Dynamics of HIV-1 replication in vivo.视角系列:宿主/病原体相互作用。HIV-1在体内的复制动态。
J Clin Invest. 1997 Jun 1;99(11):2565-7. doi: 10.1172/JCI119443.
10
Effects of (R)-9-(2-phosphonylmethoxypropyl)adenine monotherapy on chronic SIV infection in macaques.(R)-9-(2-膦酰甲氧基丙基)腺嘌呤单一疗法对猕猴慢性猴免疫缺陷病毒感染的影响。
AIDS Res Hum Retroviruses. 1997 May 20;13(8):707-12. doi: 10.1089/aid.1997.13.707.

恒河猴血浆中猿猴免疫缺陷病毒颗粒的快速清除。

Rapid clearance of simian immunodeficiency virus particles from plasma of rhesus macaques.

作者信息

Zhang L, Dailey P J, He T, Gettie A, Bonhoeffer S, Perelson A S, Ho D D

机构信息

Aaron Diamond AIDS Research Center, The Rockefeller University, New York, New York, USA.

出版信息

J Virol. 1999 Jan;73(1):855-60. doi: 10.1128/JVI.73.1.855-860.1999.

DOI:10.1128/JVI.73.1.855-860.1999
PMID:9847402
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC103903/
Abstract

Perturbation of the equilibrium between human immunodeficiency virus type 1 (HIV-1) and the infected host by administering antiretroviral agents has revealed the rapid turnover of both viral particles and productively infected cells. In this study, we used the infusion of simian immunodeficiency virus (SIV) particles into rhesus macaques to obtain a more accurate estimate of viral clearance in vivo. Consistently, exogenously infused virions were cleared from plasma with an extremely short half-life, on the order of minutes (a mean of 3.3 min). This new estimate is approximately 100-fold lower than the upper bound of 6 h previously reported for HIV-1 in infected humans. In select animals, multiple tissues were collected at the completion of each experiment to track the potential sites of virion clearance. Detectable levels of SIV RNA were found in lymph nodes, spleen, lungs, and liver, but not in other tissues examined. However, only approximately 1 to 10% or less of the infused virions were accounted for by the thorough tissue sampling, indicating that the vast majority of the infused particles must have been degraded over a short period of time. Should the rapid clearance of virions described here be applicable to infected patients, then HIV-1 production and thus the number of productively infected CD4(+) T lymphocytes or the viral burst size must be proportionally higher than previous minimal estimates.

摘要

通过施用抗逆转录病毒药物来扰动1型人类免疫缺陷病毒(HIV-1)与受感染宿主之间的平衡,已揭示出病毒颗粒和产生病毒的感染细胞的快速周转。在本研究中,我们通过向恒河猴输注猿猴免疫缺陷病毒(SIV)颗粒,以获得体内病毒清除率的更准确估计。一致地,外源性输注的病毒粒子从血浆中清除的半衰期极短,约为几分钟(平均3.3分钟)。这一新估计值比先前报道的受感染人类中HIV-1的6小时上限低约100倍。在选定的动物中,在每个实验结束时收集多个组织,以追踪病毒粒子清除的潜在部位。在淋巴结、脾脏、肺和肝脏中发现了可检测水平的SIV RNA,但在检查的其他组织中未发现。然而,通过彻底的组织采样仅发现约1%至10%或更少的输注病毒粒子,这表明绝大多数输注的粒子必定在短时间内被降解。如果此处描述的病毒粒子的快速清除适用于受感染患者,那么HIV-1的产生以及因此产生病毒的CD4(+) T淋巴细胞数量或病毒爆发大小必定比先前的最低估计值成比例地更高。