• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

在非洲绿猴长期感染猿猴免疫缺陷病毒期间,外周血与淋巴结病毒载量不存在二分法。

Lack of dichotomy between virus load of peripheral blood and lymph nodes during long-term simian immunodeficiency virus infection of African green monkeys.

作者信息

Beer B, Scherer J, zur Megede J, Norley S, Baier M, Kurth R

机构信息

Paul-Ehrlich-Institute Langen, Germany.

出版信息

Virology. 1996 May 15;219(2):367-75. doi: 10.1006/viro.1996.0262.

DOI:10.1006/viro.1996.0262
PMID:8638402
Abstract

During the asymptomatic phase of human immunodeficiency virus 1 (HIV-1) infection the lymphatic tissues seem to function as a major reservoir of HIV. We have examined the viral load in peripheral blood mononuclear cells (PBMC) and lymph node mononuclear cells (LNMC) of 12 naturally and 4 experimentally long-term simian Immunodeficiency virus (SIV)-infected African green monkeys (AGM) to help explain the apathogenicity of the AGM isolates of SIV (SIVagm) in their natural host. The mean number of SIVagm producing cells determined by limiting dilution assay was found to be 1.7 +/- 2.2 and 2.1 +/- 3.3 per 10(5) PBMC or LNMC, respectively. Similarly, polymerase chain reaction analysis of serially diluted cells showed the mean provirus carrying cell number to be 2.8 +/- 3.7 per 10(5) PBMC and 4.0 +/- 5.5 per 10(5) LNMC. When normalized for CD4+ cells the provirus and infectious virus loads in the LNMC and PBMC were also similar. No trapping of virus particles could be detected by in situ hybridization or immunohistochemistry. The data demonstrate that in contrast to HIV-1-infected humans, the viral burden in the lymph nodes of long-term SIV(agm)-infected AGMs is comparable to that in the PBMC.

摘要

在人类免疫缺陷病毒1型(HIV-1)感染的无症状期,淋巴组织似乎是HIV的主要储存库。我们检测了12只自然感染和4只实验性长期感染猿猴免疫缺陷病毒(SIV)的非洲绿猴(AGM)外周血单个核细胞(PBMC)和淋巴结单个核细胞(LNMC)中的病毒载量,以帮助解释SIV非洲绿猴分离株(SIVagm)在其自然宿主中的无致病性。通过有限稀释法测定,每10⁵个PBMC或LNMC中产生SIVagm的细胞平均数分别为1.7±2.2和2.1±3.3。同样,对连续稀释细胞进行的聚合酶链反应分析显示,每10⁵个PBMC中携带前病毒的细胞平均数为2.8±3.7,每10⁵个LNMC中为4.0±5.5。以CD4⁺细胞进行标准化后,LNMC和PBMC中的前病毒和感染性病毒载量也相似。通过原位杂交或免疫组织化学未检测到病毒颗粒的滞留。数据表明,与HIV-1感染的人类不同,长期感染SIV(agm)的AGM淋巴结中的病毒载量与PBMC中的相当。

相似文献

1
Lack of dichotomy between virus load of peripheral blood and lymph nodes during long-term simian immunodeficiency virus infection of African green monkeys.在非洲绿猴长期感染猿猴免疫缺陷病毒期间,外周血与淋巴结病毒载量不存在二分法。
Virology. 1996 May 15;219(2):367-75. doi: 10.1006/viro.1996.0262.
2
High levels of viral replication during primary simian immunodeficiency virus SIVagm infection are rapidly and strongly controlled in African green monkeys.在非洲绿猴原发性猿猴免疫缺陷病毒SIVagm感染期间,高水平的病毒复制会迅速且有力地受到控制。
J Virol. 2000 Aug;74(16):7538-47. doi: 10.1128/jvi.74.16.7538-7547.2000.
3
Quantitation of a lentivirus in its natural host: simian immunodeficiency virus in African green monkeys.慢病毒在其自然宿主中的定量分析:非洲绿猴中的猿猴免疫缺陷病毒
J Virol. 1992 Apr;66(4):2143-9. doi: 10.1128/JVI.66.4.2143-2149.1992.
4
CD8+ T lymphocytes of African green monkeys secrete an immunodeficiency virus-suppressing lymphokine.非洲绿猴的CD8 + T淋巴细胞分泌一种抑制免疫缺陷病毒的淋巴因子。
Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):7207-11. doi: 10.1073/pnas.91.15.7207.
5
DC-SIGN from African green monkeys is expressed in lymph nodes and mediates infection in trans of simian immunodeficiency virus SIVagm.来自非洲绿猴的DC-SIGN在淋巴结中表达,并介导猴免疫缺陷病毒SIVagm的跨细胞感染。
J Virol. 2004 Jan;78(2):798-810. doi: 10.1128/jvi.78.2.798-810.2004.
6
Wide range of viral load in healthy african green monkeys naturally infected with simian immunodeficiency virus.自然感染猿猴免疫缺陷病毒的健康非洲绿猴体内病毒载量范围广泛。
J Virol. 2000 Dec;74(24):11744-53. doi: 10.1128/jvi.74.24.11744-11753.2000.
7
CXCR6-Mediated Simian Immunodeficiency Virus SIVagmSab Entry into Sabaeus African Green Monkey Lymphocytes Implicates Widespread Use of Non-CCR5 Pathways in Natural Host Infections.CXCR6介导的猴免疫缺陷病毒SIVagmSab进入非洲绿猴淋巴细胞表明非CCR5途径在自然宿主感染中广泛使用。
J Virol. 2017 Jan 31;91(4). doi: 10.1128/JVI.01626-16. Print 2017 Feb 15.
8
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.
9
Simian immunodeficiency virus SIVagm.sab infection of Caribbean African green monkeys: a new model for the study of SIV pathogenesis in natural hosts.猿猴免疫缺陷病毒SIVagm.sab对加勒比非洲绿猴的感染:一种研究自然宿主中SIV发病机制的新模型。
J Virol. 2006 May;80(10):4858-67. doi: 10.1128/JVI.80.10.4858-4867.2006.
10
SIVagm: genetic and biological features associated with replication.猴免疫缺陷病毒(SIVagm):与复制相关的遗传和生物学特征
Front Biosci. 2003 Sep 1;8:d1170-85. doi: 10.2741/1130.

引用本文的文献

1
DNA methylation changes in metabolic and immune-regulatory pathways in blood and lymph node CD4 + T cells in response to SIV infections.针对 SIV 感染,血液和淋巴结 CD4+T 细胞中代谢和免疫调节途径中的 DNA 甲基化变化。
Clin Epigenetics. 2020 Dec 9;12(1):188. doi: 10.1186/s13148-020-00971-w.
2
Lymph Node Cellular and Viral Dynamics in Natural Hosts and Impact for HIV Cure Strategies.在天然宿主中淋巴结细胞和病毒动态及其对 HIV 治愈策略的影响。
Front Immunol. 2018 Apr 19;9:780. doi: 10.3389/fimmu.2018.00780. eCollection 2018.
3
Loss of CXCR6 coreceptor usage characterizes pathogenic lentiviruses.
CXCR6 辅助受体使用的丧失是致病性慢病毒的特征。
PLoS Pathog. 2018 Apr 16;14(4):e1007003. doi: 10.1371/journal.ppat.1007003. eCollection 2018 Apr.
4
Control of HIV-1 Pathogenesis in Viremic Nonprogressors Is Independent of Gag-Specific Cytotoxic T Lymphocyte Responses.病毒血症非进展者中 HIV-1 发病机制的控制与 Gag 特异性细胞毒性 T 淋巴细胞反应无关。
J Virol. 2018 May 29;92(12). doi: 10.1128/JVI.00346-18. Print 2018 Jun 15.
5
Predominant envelope variable loop 2-specific and gp120-specific antibody-dependent cellular cytotoxicity antibody responses in acutely SIV-infected African green monkeys.急性 SIV 感染的非洲绿猴中优势包膜可变环 2 特异性和 gp120 特异性抗体依赖性细胞细胞毒性抗体反应。
Retrovirology. 2018 Mar 9;15(1):24. doi: 10.1186/s12977-018-0406-5.
6
The B-Cell Follicle in HIV Infection: Barrier to a Cure.HIV 感染中的 B 细胞滤泡:治愈的障碍。
Front Immunol. 2018 Jan 25;9:20. doi: 10.3389/fimmu.2018.00020. eCollection 2018.
7
Natural killer cells migrate into and control simian immunodeficiency virus replication in lymph node follicles in African green monkeys.自然杀伤细胞迁移至非洲绿猴的淋巴结滤泡中,并控制猿猴免疫缺陷病毒在其中的复制。
Nat Med. 2017 Nov;23(11):1277-1286. doi: 10.1038/nm.4421. Epub 2017 Oct 16.
8
CXCR6-Mediated Simian Immunodeficiency Virus SIVagmSab Entry into Sabaeus African Green Monkey Lymphocytes Implicates Widespread Use of Non-CCR5 Pathways in Natural Host Infections.CXCR6介导的猴免疫缺陷病毒SIVagmSab进入非洲绿猴淋巴细胞表明非CCR5途径在自然宿主感染中广泛使用。
J Virol. 2017 Jan 31;91(4). doi: 10.1128/JVI.01626-16. Print 2017 Feb 15.
9
Envelope-specific B-cell populations in African green monkeys chronically infected with simian immunodeficiency virus.慢性感染猴免疫缺陷病毒的非洲绿猴体内的信封特异性 B 细胞群体。
Nat Commun. 2016 Jul 6;7:12131. doi: 10.1038/ncomms12131.
10
HIV-associated chronic immune activation.HIV 相关的慢性免疫激活。
Immunol Rev. 2013 Jul;254(1):78-101. doi: 10.1111/imr.12079.