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2
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Monotypic low-level HIV viremias during antiretroviral therapy are associated with disproportionate production of X4 virions and systemic immune activation.在抗逆转录病毒治疗期间,单型低水平 HIV 病毒血症与不成比例的 X4 病毒粒子产生和全身免疫激活有关。
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1
Monotypic low-level HIV viremias during antiretroviral therapy are associated with disproportionate production of X4 virions and systemic immune activation.在抗逆转录病毒治疗期间,单型低水平 HIV 病毒血症与不成比例的 X4 病毒粒子产生和全身免疫激活有关。
AIDS. 2018 Jul 17;32(11):1389-1401. doi: 10.1097/QAD.0000000000001824.
2
Clonal Expansion of Human Immunodeficiency Virus-Infected Cells and Human Immunodeficiency Virus Persistence During Antiretroviral Therapy.抗逆转录病毒治疗期间人类免疫缺陷病毒感染细胞的克隆扩增及人类免疫缺陷病毒持续存在
J Infect Dis. 2017 Mar 15;215(suppl_3):S119-S127. doi: 10.1093/infdis/jiw636.
3
Quantification of Residual Germinal Center Activity and HIV-1 DNA and RNA Levels Using Fine Needle Biopsies of Lymph Nodes During Antiretroviral Therapy.在抗逆转录病毒治疗期间,使用淋巴结细针穿刺活检对残留生发中心活性以及HIV-1 DNA和RNA水平进行定量分析。
AIDS Res Hum Retroviruses. 2017 Jul;33(7):648-657. doi: 10.1089/aid.2016.0171. Epub 2017 Mar 13.
4
Therapeutic Immune Recovery and Reduction of CXCR4-Tropic HIV-1.治疗性免疫恢复和降低 CXCR4 嗜性 HIV-1。
Clin Infect Dis. 2017 Feb 1;64(3):295-300. doi: 10.1093/cid/ciw737. Epub 2016 Nov 12.
5
New insights into the heterogeneity of Th17 subsets contributing to HIV-1 persistence during antiretroviral therapy.关于抗逆转录病毒治疗期间促成HIV-1持续存在的Th17亚群异质性的新见解。
Retrovirology. 2016 Aug 24;13(1):59. doi: 10.1186/s12977-016-0293-6.
6
Clonally expanded CD4+ T cells can produce infectious HIV-1 in vivo.克隆扩增的CD4+ T细胞可在体内产生具有传染性的HIV-1。
Proc Natl Acad Sci U S A. 2016 Feb 16;113(7):1883-8. doi: 10.1073/pnas.1522675113. Epub 2016 Feb 8.
7
Origin of Rebound Plasma HIV Includes Cells with Identical Proviruses That Are Transcriptionally Active before Stopping of Antiretroviral Therapy.反弹血浆HIV的起源包括在抗逆转录病毒治疗停止前具有转录活性的携带相同前病毒的细胞。
J Virol. 2015 Nov 18;90(3):1369-76. doi: 10.1128/JVI.02139-15. Print 2016 Feb 1.
8
Large number of rebounding/founder HIV variants emerge from multifocal infection in lymphatic tissues after treatment interruption.治疗中断后,大量反弹/失活的HIV变异体在淋巴组织的多灶性感染中出现。
Proc Natl Acad Sci U S A. 2015 Mar 10;112(10):E1126-34. doi: 10.1073/pnas.1414926112. Epub 2015 Feb 23.
9
Inguinal lymph node and anorectal mucosal biopsies for human immunodeficiency virus research protocols in an emerging nation: patient outcomes and lessons learned.新兴国家中用于人类免疫缺陷病毒研究方案的腹股沟淋巴结和肛门直肠黏膜活检:患者结局及经验教训
Surg Infect (Larchmt). 2015 Feb;16(1):68-71. doi: 10.1089/sur.2013.179. Epub 2015 Feb 4.
10
The importance of viral blips and duration of therapy initiated in primary infection in maintaining viral control after stopping cART.原发性感染中出现的病毒波动及开始治疗的持续时间对于停止抗逆转录病毒治疗(cART)后维持病毒控制的重要性。
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将病毒学失败时血浆中的HIV序列与先前抗逆转录病毒治疗抑制时宫颈与血液序列进行比较的系统发育分析。

Phylogenetic Analyses Comparing HIV Sequences from Plasma at Virologic Failure to Cervix Versus Blood Sequences from Antecedent Antiretroviral Therapy Suppression.

作者信息

Bull Marta E, McKernan Jennifer L, Styrchak Sheila, Kraft Kelli, Hitti Jane, Cohn Susan E, Tapia Kenneth, Deng Wenjie, Holte Sarah, Mullins James I, Coombs Robert W, Frenkel Lisa M

机构信息

1 Department of Pediatrics, University of Washington, Seattle, Washington.

2 Center Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, Washington.

出版信息

AIDS Res Hum Retroviruses. 2019 Jun;35(6):557-566. doi: 10.1089/AID.2018.0211. Epub 2019 Apr 30.

DOI:10.1089/AID.2018.0211
PMID:30892052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6588103/
Abstract

Identifying tissue sources of HIV that rebound following "failure" of antiretroviral therapy (ART) is critical to evaluating cure strategies. To assess the role of the uterine cervix and peripheral blood mononuclear cells (PBMC) as viral reservoirs, nearest-neighbor phylogenetic analyses compared genetic relatedness of tissue sequences during ART suppression to those detected in plasma at viral rebound. Blood and genital tract specimens from a natural history cohort of HIV-infected women were collected over 5 years. HIV DNA sequences extracted from PBMC and cervical biopsies during ART suppression and plasma RNA from rebound (defined as HIV RNA >3 log copies/mL) were derived by single-genome amplification. Phylogenetic and nearest-neighbor analyses of HIV sequences and drug resistance in sequences were compared between tissues. Nine instances of plasma viral rebound (median HIV RNA 3.6 log c/mL; IQR: 3.1-3.8) were detected in 7 of 57 women. Nearest-neighbor analyses found rebound plasma sequences were closer to uterine cervical sequences in 4/9 (44%), closer to PBMC in 3/9 (33%), and ambiguous in 2/9 (22%) cases. Rebound plasma clades ( = 27) shared identical sequences in seven instances with the cervix versus two with PBMC. Novel drug resistance mutations were detected in 4/9 (44%) rebounds. The observed tendency for greater sharing of identical HIV variants and greater nearest-neighbor association between rebounding plasma and uterine cervical versus PBMC sequences suggests that the uterine cervix may be a relevant HIV reservoir. The cervix, a readily accessible tissue in women that can be repeatedly sampled, could help assess the HIV reservoir when evaluating cure strategies.

摘要

确定抗逆转录病毒疗法(ART)“失败”后反弹的HIV组织来源对于评估治愈策略至关重要。为了评估子宫颈和外周血单个核细胞(PBMC)作为病毒储存库的作用,最近邻系统发育分析比较了ART抑制期间组织序列与病毒反弹时血浆中检测到的序列的遗传相关性。在5年多的时间里收集了来自HIV感染女性自然史队列的血液和生殖道标本。通过单基因组扩增获得ART抑制期间从PBMC和宫颈活检中提取的HIV DNA序列以及反弹时(定义为HIV RNA>3 log拷贝/mL)的血浆RNA。比较了组织之间HIV序列的系统发育和最近邻分析以及序列中的耐药性。在57名女性中的7名中检测到9例血浆病毒反弹(HIV RNA中位数为3.6 log c/mL;IQR:3.1-3.8)。最近邻分析发现,在4/9(44%)的病例中,反弹血浆序列更接近子宫颈序列,在3/9(33%)的病例中更接近PBMC,在2/9(22%)的病例中不明确。反弹血浆分支(=27)在7例中与子宫颈共享相同序列,而与PBMC共享相同序列的有2例。在4/9(44%)的反弹中检测到新的耐药突变。观察到的相同HIV变体更大程度共享的趋势以及反弹血浆与子宫颈序列而非PBMC序列之间更强的最近邻关联表明,子宫颈可能是一个相关的HIV储存库。子宫颈是女性中易于获取且可重复采样的组织,在评估治愈策略时有助于评估HIV储存库。