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Acute loss of intestinal CD4+ T cells is not predictive of simian immunodeficiency virus virulence.肠道CD4+ T细胞的急性丧失不能预测猿猴免疫缺陷病毒的毒力。
J Immunol. 2007 Sep 1;179(5):3035-46. doi: 10.4049/jimmunol.179.5.3035.
2
The AIDS resistance of naturally SIV-infected sooty mangabeys is independent of cellular immunity to the virus.自然感染猴免疫缺陷病毒的乌黑白眉猴对艾滋病的抵抗力与针对该病毒的细胞免疫无关。
Blood. 2006 Jul 1;108(1):209-17. doi: 10.1182/blood-2005-12-4897. Epub 2006 Mar 7.
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Kuru experiments triggered the emergence of pathogenic SIVmac.库鲁病实验引发了致病性猴免疫缺陷病毒(SIVmac)的出现。
AIDS. 2006 Feb 14;20(3):317-21. doi: 10.1097/01.aids.0000206498.71041.0e.
4
Immunodeficiency in the absence of high viral load in pig-tailed macaques infected with Simian immunodeficiency virus SIVsun or SIVlhoest.感染猴免疫缺陷病毒SIVsun或SIVlhoest的猪尾猕猴在病毒载量不高的情况下出现免疫缺陷。
J Virol. 2005 Nov;79(22):14044-56. doi: 10.1128/JVI.79.22.14044-14056.2005.
5
Simian immunodeficiency virus infection in free-ranging sooty mangabeys (Cercocebus atys atys) from the Taï Forest, Côte d'Ivoire: implications for the origin of epidemic human immunodeficiency virus type 2.来自科特迪瓦的塔伊森林中自由放养的黑猩猩(Cercocebus atys atys)感染猿猴免疫缺陷病毒:对2型流行性人类免疫缺陷病毒起源的影响。
J Virol. 2005 Oct;79(19):12515-27. doi: 10.1128/JVI.79.19.12515-12527.2005.
6
Differential restriction of human immunodeficiency virus type 2 and simian immunodeficiency virus SIVmac by TRIM5alpha alleles.TRIM5α等位基因对2型人类免疫缺陷病毒和猴免疫缺陷病毒SIVmac的差异性限制
J Virol. 2005 Sep;79(18):11580-7. doi: 10.1128/JVI.79.18.11580-11587.2005.
7
Naturally SIV-infected sooty mangabeys: are we closer to understanding why they do not develop AIDS?自然感染SIV的黑猩猩:我们离理解它们为何不会患上艾滋病更近一步了吗?
J Med Primatol. 2005 Oct;34(5-6):243-52. doi: 10.1111/j.1600-0684.2005.00122.x.
8
Molecular epidemiology of simian immunodeficiency virus SIVsm in U.S. primate centers unravels the origin of SIVmac and SIVstm.美国灵长类动物中心猿猴免疫缺陷病毒SIVsm的分子流行病学揭示了SIVmac和SIVstm的起源。
J Virol. 2005 Jul;79(14):8991-9005. doi: 10.1128/JVI.79.14.8991-9005.2005.
9
Plateau levels of viremia correlate with the degree of CD4+-T-cell loss in simian immunodeficiency virus SIVagm-infected pigtailed macaques: variable pathogenicity of natural SIVagm isolates.在感染猿猴免疫缺陷病毒SIVagm的猪尾猕猴中,病毒血症的平台期水平与CD4 + T细胞损失程度相关:天然SIVagm分离株的致病性各异 。
J Virol. 2005 Apr;79(8):5153-62. doi: 10.1128/JVI.79.8.5153-5162.2005.
10
Cytidine deamination and resistance to retroviral infection: towards a structural understanding of the APOBEC proteins.胞苷脱氨基作用与抗逆转录病毒感染:对载脂蛋白B mRNA编辑酶催化多肽样蛋白(APOBEC)的结构理解
Virology. 2005 Apr 10;334(2):147-53. doi: 10.1016/j.virol.2005.01.038.

不同谱系的原发性猴免疫缺陷病毒(SIVsmm)分离株的体外特性。在恒河猴细胞上的体外生长情况并不能预测其在恒河猴体内的复制情况。

In vitro characterization of primary SIVsmm isolates belonging to different lineages. In vitro growth on rhesus macaque cells is not predictive for in vivo replication in rhesus macaques.

作者信息

Gautam Rajeev, Carter Anders Chase, Katz Nathalia, Butler Isolde F, Barnes Mary, Hasegawa Atsuhiko, Ratterree Marion, Silvestri Guido, Marx Preston A, Hirsch Vanessa M, Pandrea Ivona, Apetrei Cristian

机构信息

Division of Microbiology, Tulane National Primate Research Center, Covington, LA 70433, USA.

出版信息

Virology. 2007 Jun 5;362(2):257-70. doi: 10.1016/j.virol.2006.12.037. Epub 2007 Feb 15.

DOI:10.1016/j.virol.2006.12.037
PMID:17303205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1936220/
Abstract

We report in vitro characterization of 11 SIVsmm strains of six lineages co-circulating in naturally infected sooty mangabeys (SMs) from US Primate Centers and showed no major differences in the in vitro replication pattern between different SIVsmm lineages. Primary SIVsmm isolates utilized CCR5 and Bonzo co-receptors in vitro. SIVsmm growth in human T cell lines was isolate-, not lineage-specific, with poor replication on Molt4-Clone8, CEMss and PM1 cells and better replication on MT2, SupT1 and CEMx174 cells. All primary SIVsmm isolates replicated on SM and human PBMCs. In vitro replication in macaques varied widely, with moderate to high replication in pig-tailed macaque PBMCs, enhanced by CD8+ T cell depletion, and highly variable replication on rhesus macaque (Rh) PBMCs. Primary SIVsmm isolates replicated in Rh monocyte-derived dendritic cells (MDDCs) and monocyte-derived macrophages (MDMs). In vivo, SIVsmm isolates replicated at high levels in all SIVsmm-infected Rh. The poor in vitro replication of primary SIVsmm isolates in Rh cells did not correlate with in vivo replication, emphasizing the value of in vivo studies.

摘要

我们报告了来自美国灵长类动物中心自然感染的乌黑白眉猴(SM)中共同传播的六个谱系的11种SIVsmm毒株的体外特性,结果显示不同SIVsmm谱系之间的体外复制模式没有重大差异。原发性SIVsmm分离株在体外利用CCR5和Bonzo共受体。SIVsmm在人T细胞系中的生长具有分离株特异性,而非谱系特异性,在Molt4-Clone8、CEMss和PM1细胞上复制较差,在MT2、SupT1和CEMx174细胞上复制较好。所有原发性SIVsmm分离株均能在SM和人外周血单核细胞(PBMC)上复制。在猕猴中的体外复制差异很大,在猪尾猕猴PBMC中复制为中度至高,CD8 + T细胞耗竭可增强复制,而在恒河猴(Rh)PBMC上的复制高度可变。原发性SIVsmm分离株能在Rh单核细胞衍生的树突状细胞(MDDC)和单核细胞衍生的巨噬细胞(MDM)中复制。在体内,SIVsmm分离株在所有感染SIVsmm的Rh中高水平复制。原发性SIVsmm分离株在Rh细胞中的体外复制较差与体内复制无关,强调了体内研究的价值。