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本文引用的文献

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Defining HIV and SIV Reservoirs in Lymphoid Tissues.确定淋巴组织中的HIV和SIV储存库。
Pathog Immun. 2016 Spring;1(1):68-106. doi: 10.20411/pai.v1i1.100.
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Diversity of HIV-1 reservoirs in CD4+ T-cell subpopulations.CD4+ T细胞亚群中HIV-1储存库的多样性。
Curr Opin HIV AIDS. 2016 Jul;11(4):383-7. doi: 10.1097/COH.0000000000000281.
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Dissecting How CD4 T Cells Are Lost During HIV Infection.剖析HIV感染期间CD4 T细胞是如何丧失的。
Cell Host Microbe. 2016 Mar 9;19(3):280-91. doi: 10.1016/j.chom.2016.02.012.
4
Loss of Function of Intestinal IL-17 and IL-22 Producing Cells Contributes to Inflammation and Viral Persistence in SIV-Infected Rhesus Macaques.肠道中产生白细胞介素-17和白细胞介素-22的细胞功能丧失导致了感染猴免疫缺陷病毒的恒河猴的炎症和病毒持续存在。
PLoS Pathog. 2016 Feb 1;12(2):e1005412. doi: 10.1371/journal.ppat.1005412. eCollection 2016 Feb.
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Persistent HIV-1 replication maintains the tissue reservoir during therapy.在治疗期间,持续的HIV-1复制维持着组织储存库。
Nature. 2016 Feb 4;530(7588):51-56. doi: 10.1038/nature16933. Epub 2016 Jan 27.
6
HIV-1 Env Glycoprotein Phenotype along with Immune Activation Determines CD4 T Cell Loss in HIV Patients.HIV-1包膜糖蛋白表型与免疫激活共同决定HIV患者CD4 T细胞的损失。
J Immunol. 2016 Feb 15;196(4):1768-79. doi: 10.4049/jimmunol.1501588. Epub 2016 Jan 13.
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Follicular Dendritic Cells Retain Infectious HIV in Cycling Endosomes.滤泡树突状细胞在循环内体中保留感染性HIV。
PLoS Pathog. 2015 Dec 1;11(12):e1005285. doi: 10.1371/journal.ppat.1005285. eCollection 2015 Dec.
8
Persistent Simian Immunodeficiency Virus Infection Causes Ultimate Depletion of Follicular Th Cells in AIDS.持续性猿猴免疫缺陷病毒感染导致艾滋病患者滤泡辅助性T细胞最终耗竭。
J Immunol. 2015 Nov 1;195(9):4351-7. doi: 10.4049/jimmunol.1501273. Epub 2015 Sep 25.
9
Decreased T Follicular Regulatory Cell/T Follicular Helper Cell (TFH) in Simian Immunodeficiency Virus-Infected Rhesus Macaques May Contribute to Accumulation of TFH in Chronic Infection.感染猿猴免疫缺陷病毒的恒河猴中滤泡调节性T细胞/滤泡辅助性T细胞(TFH)减少可能导致慢性感染中TFH的积累。
J Immunol. 2015 Oct 1;195(7):3237-47. doi: 10.4049/jimmunol.1402701. Epub 2015 Aug 21.
10
Experimental colitis in SIV-uninfected rhesus macaques recapitulates important features of pathogenic SIV infection.未感染SIV的恒河猴的实验性结肠炎重现了致病性SIV感染的重要特征。
Nat Commun. 2015 Aug 18;6:8020. doi: 10.1038/ncomms9020.

对非人灵长类动物的淋巴组织进行成像以了解猴免疫缺陷病毒的发病机制和持续性。

Imaging lymphoid tissues in nonhuman primates to understand SIV pathogenesis and persistence.

作者信息

Deleage Claire, Turkbey Baris, Estes Jacob D

机构信息

AIDS and Cancer Virus Program, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, BG 535, Post Office Box B, Frederick, MD 21702, USA.

Molecular Imaging Program, National Cancer Institute, Building 10, Room B3B69F, Bethesda, MD 20814, USA.

出版信息

Curr Opin Virol. 2016 Aug;19:77-84. doi: 10.1016/j.coviro.2016.07.002. Epub 2016 Aug 1.

DOI:10.1016/j.coviro.2016.07.002
PMID:27490446
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5021606/
Abstract

CD4+ T cells are the primary HIV-1 target cell, with the vast majority of these cells residing within lymphoid tissue compartments throughout the body. Predictably, HIV-1 infection, replication, localization, reservoir establishment and persistence, as well as associated host immune and inflammatory responses and disease pathology principally take place within the tissues of the immune system. By virture of the fact that the virus-host struggle is played out within lymphoid and additional tissues compartments in HIV-1 infected individuals it is critical to understand HIV-1 infection and disease within these relevant tissue sites; however, there are obvious limitations to studying these dynamic processes in humans. Nonhuman primate (NHP) research has provided a vital bridge between basic and preclinical research and clinical studies, with experimental SIV infection of NHP models offering unique opportunities to understand key processes of HIV-1 infection and disease that are either not practically feasible or ethical in HIV-1 infected humans. In this review we will discuss current approaches to studying the tissue based immunopathogenesis of AIDS virus infection in NHPs, including both analyses of tissues obtained at biopsy or necropsy and complementary non-invasive imaging approaches that may have practical utility in monitoring HIV-1 disease in the clinical setting.

摘要

CD4+ T细胞是HIV-1的主要靶细胞,其中绝大多数细胞存在于全身的淋巴组织隔室中。可以预见的是,HIV-1感染、复制、定位、储存库的建立和维持,以及相关的宿主免疫和炎症反应及疾病病理主要发生在免疫系统组织内。由于病毒与宿主的斗争在HIV-1感染个体的淋巴组织和其他组织隔室中展开,了解这些相关组织部位的HIV-1感染和疾病至关重要;然而,在人体中研究这些动态过程存在明显局限性。非人灵长类动物(NHP)研究在基础研究、临床前研究和临床研究之间架起了一座重要桥梁,对NHP模型进行实验性SIV感染为了解HIV-1感染和疾病的关键过程提供了独特机会,而这些过程在HIV-1感染的人类中要么在实际操作上不可行,要么不符合伦理。在本综述中,我们将讨论目前研究NHP中艾滋病病毒感染的组织免疫发病机制的方法,包括对活检或尸检获取的组织进行分析,以及在临床环境中监测HIV-1疾病可能具有实际应用价值的补充性非侵入性成像方法。