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Characterization of HIV-1 RNA forms in the plasma of patients undergoing successful HAART.对接受高效抗逆转录病毒治疗(HAART)的患者血浆中 HIV-1 RNA 形式的特征分析。
Arch Virol. 2010 Jun;155(6):895-903. doi: 10.1007/s00705-010-0659-3. Epub 2010 Apr 23.
2
HIV-1 infects multipotent progenitor cells causing cell death and establishing latent cellular reservoirs.HIV-1 感染多能祖细胞,导致细胞死亡并建立潜伏的细胞储库。
Nat Med. 2010 Apr;16(4):446-51. doi: 10.1038/nm.2109. Epub 2010 Mar 7.
3
Viral sanctuaries during highly active antiretroviral therapy in a nonhuman primate model for AIDS.在艾滋病非人灵长类动物模型中,高效抗逆转录病毒治疗期间的病毒避难所。
J Virol. 2010 Mar;84(6):2913-22. doi: 10.1128/JVI.02356-09. Epub 2009 Dec 23.
4
Failure to detect active virus replication in mast cells at various tissue sites of HIV patients by immunohistochemistry.免疫组织化学未能在 HIV 患者的各种组织部位的肥大细胞中检测到活跃的病毒复制。
Int J Biol Sci. 2009 Sep 22;5(6):603-10. doi: 10.7150/ijbs.5.603.
5
Profile of hematological abnormalities of Indian HIV infected individuals.印度艾滋病毒感染者的血液学异常情况概述。
BMC Blood Disord. 2009 Aug 13;9:5. doi: 10.1186/1471-2326-9-5.
6
Analysis of human immunodeficiency virus type 1 viremia and provirus in resting CD4+ T cells reveals a novel source of residual viremia in patients on antiretroviral therapy.对1型人类免疫缺陷病毒血症和静息CD4+ T细胞中前病毒的分析揭示了接受抗逆转录病毒治疗患者残余病毒血症的新来源。
J Virol. 2009 Sep;83(17):8470-81. doi: 10.1128/JVI.02568-08. Epub 2009 Jun 17.
7
IgE-FcepsilonRI interactions determine HIV coreceptor usage and susceptibility to infection during ontogeny of mast cells.IgE与FcεRI的相互作用决定了肥大细胞发育过程中HIV共受体的使用情况及感染易感性。
J Immunol. 2009 May 15;182(10):6401-9. doi: 10.4049/jimmunol.0801481.
8
HIV-1 infection of bone marrow hematopoietic progenitor cells and their role in trafficking and viral dissemination.人类免疫缺陷病毒1型对骨髓造血祖细胞的感染及其在细胞迁移和病毒播散中的作用。
PLoS Pathog. 2008 Dec;4(12):e1000215. doi: 10.1371/journal.ppat.1000215. Epub 2008 Dec 26.
9
Low-level plasma HIVs in patients on prolonged suppressive highly active antiretroviral therapy are produced mostly by cells other than CD4 T-cells.接受长期抑制性高效抗逆转录病毒治疗的患者体内的低水平血浆HIV大多由CD4 T细胞以外的细胞产生。
J Med Virol. 2009 Jan;81(1):9-15. doi: 10.1002/jmv.21366.
10
HIV rebounds from latently infected cells, rather than from continuing low-level replication.HIV从潜伏感染的细胞中反弹,而非源于持续的低水平复制。
Proc Natl Acad Sci U S A. 2008 Oct 28;105(43):16725-30. doi: 10.1073/pnas.0804192105. Epub 2008 Oct 20.

造血干细胞/祖细胞作为 HIV 的储存库。

Hematopoietic stem/precursor cells as HIV reservoirs.

机构信息

Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, USA.

出版信息

Curr Opin HIV AIDS. 2011 Jan;6(1):43-8. doi: 10.1097/COH.0b013e32834086b3.

DOI:10.1097/COH.0b013e32834086b3
PMID:21242893
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3045752/
Abstract

PURPOSE OF REVIEW

Although latent HIV-1 infection in CD4+ T cells contributes to HIV persistence, there is mounting evidence that other viral reservoirs exist. Here, we review recent data suggesting that the infection of hematopoietic progenitor cells creates additional reservoirs for HIV in vivo.

RECENT FINDINGS

New studies suggest that some types of hematopoietic progenitor cells have the potential to generate reservoirs for HIV. This review focuses on two types that can be infected by HIV in vitro and in vivo: multipotent hematopoietic progenitor cells in the bone marrow and circulating mast cell progenitors. Of these two types, only CD34+ bone marrow cells have been shown to harbor latent provirus in HIV-positive individuals with undetectable viral loads on highly active antiretroviral therapy (HAART). Latent infection of these long-lived cell types may create a significant barrier to HIV eradication; the infection of hematopoietic stem cells in particular could lead to an HIV reservoir that does not appreciably decay over the lifespan of the host.

SUMMARY

To eradicate HIV infection, it will be necessary to purge all viral reservoirs in the host. The findings highlighted here suggest that multipotent hematopoietic progenitor cells and possibly tissue mast cells may constitute significant reservoirs for HIV that must be addressed in order to eliminate HIV infection. Future studies are needed to determine which types of CD34+ cells are infected in vivo and whether infected CD34+ cells contribute to residual viremia in people with undetectable viral loads on HAART.

摘要

目的综述

虽然潜伏的 HIV-1 感染 CD4+T 细胞有助于 HIV 持续存在,但越来越多的证据表明存在其他病毒库。在这里,我们回顾了最近的数据,这些数据表明造血祖细胞的感染在体内为 HIV 创造了额外的储库。

最新发现

新的研究表明,某些类型的造血祖细胞有可能产生 HIV 的储库。这篇综述集中讨论了两种可在体外和体内被 HIV 感染的类型:骨髓中的多能造血祖细胞和循环中的肥大细胞祖细胞。在这些类型中,只有 CD34+骨髓细胞已被证明在接受高效抗逆转录病毒治疗(HAART)的 HIV 阳性个体中携带潜伏性前病毒,这些个体的病毒载量无法检测。这些长寿细胞类型的潜伏感染可能是 HIV 根除的一个重大障碍;特别是造血干细胞的感染可能导致 HIV 储库在宿主的寿命内不会明显衰减。

总结

为了根除 HIV 感染,有必要清除宿主中的所有病毒储库。这里强调的发现表明,多能造血祖细胞和可能的组织肥大细胞可能是 HIV 的重要储库,必须加以解决,以消除 HIV 感染。未来的研究需要确定哪种类型的 CD34+细胞在体内被感染,以及感染的 CD34+细胞是否会导致接受 HAART 治疗病毒载量无法检测的个体中残留病毒血症。