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本文引用的文献

1
Inability of plasmacytoid dendritic cells to directly lyse HIV-infected autologous CD4+ T cells despite induction of tumor necrosis factor-related apoptosis-inducing ligand.尽管诱导了肿瘤坏死因子相关凋亡诱导配体,但浆细胞样树突状细胞无法直接裂解感染 HIV 的自体 CD4+ T 细胞。
J Virol. 2010 Mar;84(6):2762-73. doi: 10.1128/JVI.01350-09. Epub 2009 Dec 30.
2
Nonpathogenesis of simian immunodeficiency virus infection is associated with reduced inflammation and recruitment of plasmacytoid dendritic cells to lymph nodes, not to lack of an interferon type I response, during the acute phase.在急性期,非致病性猴免疫缺陷病毒感染与炎症减少和浆细胞样树突状细胞向淋巴结的募集有关,而与缺乏Ⅰ型干扰素反应无关。
J Virol. 2010 Feb;84(4):1838-46. doi: 10.1128/JVI.01496-09. Epub 2009 Nov 25.
3
Defective plasmacytoid dendritic cell-NK cell cross-talk in HIV infection.HIV感染中浆细胞样树突状细胞与自然杀伤细胞之间的串扰缺陷。
AIDS Res Hum Retroviruses. 2009 Oct;25(10):1029-37. doi: 10.1089/aid.2008.0311.
4
Impaired plasmacytoid dendritic cell (PDC)-NK cell activity in viremic human immunodeficiency virus infection attributable to impairments in both PDC and NK cell function.在病毒血症性人类免疫缺陷病毒感染中,浆细胞样树突状细胞(PDC)-自然杀伤细胞(NK细胞)活性受损,这归因于PDC和NK细胞功能均受损。
J Virol. 2009 Nov;83(21):11175-87. doi: 10.1128/JVI.00753-09. Epub 2009 Aug 19.
5
Plasmacytoid dendritic cells express TRAIL and induce CD4+ T-cell apoptosis in HIV-1 viremic patients.浆细胞样树突状细胞表达肿瘤坏死因子相关凋亡诱导配体(TRAIL)并在HIV-1病毒血症患者中诱导CD4 + T细胞凋亡。
Blood. 2009 Oct 29;114(18):3854-63. doi: 10.1182/blood-2009-04-217927. Epub 2009 Aug 18.
6
Sex differences in the Toll-like receptor-mediated response of plasmacytoid dendritic cells to HIV-1.浆细胞样树突状细胞对HIV-1的Toll样受体介导反应中的性别差异。
Nat Med. 2009 Aug;15(8):955-9. doi: 10.1038/nm.2004. Epub 2009 Jul 13.
7
Exogenous HIV-1 Vpr disrupts IFN-alpha response by plasmacytoid dendritic cells (pDCs) and subsequent pDC/NK interplay.外源性HIV-1病毒蛋白R(Vpr)破坏浆细胞样树突状细胞(pDCs)的Ⅰ型干扰素(IFN-α)应答以及随后的pDC/自然杀伤细胞(NK)相互作用。
Immunol Lett. 2009 Aug 15;125(2):100-4. doi: 10.1016/j.imlet.2009.06.008. Epub 2009 Jun 25.
8
Rapid influx and death of plasmacytoid dendritic cells in lymph nodes mediate depletion in acute simian immunodeficiency virus infection.淋巴结中浆细胞样树突状细胞的快速流入和死亡介导了急性猿猴免疫缺陷病毒感染中的细胞耗竭。
PLoS Pathog. 2009 May;5(5):e1000413. doi: 10.1371/journal.ppat.1000413. Epub 2009 May 8.
9
Plasmacytoid dendritic cells accumulate in spleens from chronically HIV-infected patients but barely participate in interferon-alpha expression.浆细胞样树突状细胞在慢性HIV感染患者的脾脏中积聚,但几乎不参与α干扰素的表达。
Blood. 2009 Jun 11;113(24):6112-9. doi: 10.1182/blood-2008-07-170803. Epub 2009 Apr 14.
10
Surface phenotype and rapid quantification of blood dendritic cell subsets in the rhesus macaque.恒河猴血液中树突状细胞亚群的表面表型及快速定量分析
J Med Primatol. 2009 Aug;38(4):272-8. doi: 10.1111/j.1600-0684.2009.00353.x. Epub 2009 Mar 31.

HIV 感染中的浆细胞样树突状细胞:微妙的平衡。

Plasmacytoid dendritic cells in HIV infection: striking a delicate balance.

机构信息

New Jersey Medical School, University of Medicine and Dentistry of New Jersey, Newark, New Jersey, USA.

出版信息

J Leukoc Biol. 2010 Apr;87(4):609-20. doi: 10.1189/jlb.0909635. Epub 2010 Feb 9.

DOI:10.1189/jlb.0909635
PMID:20145197
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2858309/
Abstract

pDC are the most potent IFN-alpha-producing cells in the body and serve as a vital link between innate and adaptive immunity. Deficiencies in pDC function were among the earliest observations of immune dysfunction in HIV-1 infection. Herein, we review the status of pDC in individuals with HIV-1 infection and the potential role of these cells in pathogenesis. We begin by reviewing the basic properties of pDC and then discuss the compromise in circulating pDC numbers and function in early and viremic HIV-1 infection and mechanisms that might account for their depletion in HIV-infected patients. In addition, we review the evidence that chronic production of IFN-alpha, probably through the chronic activation of pDC, is central to the immune activation that is so detrimental in HIV infection. Finally, we discuss the importance of balance in pDC numbers and function and the potential value of using absolute pDC counts and function as a biomarker, along with CD4(+) cell counts and VL in HIV-1-infected patients.

摘要

pDC 是体内最具效产生 IFN-α 的细胞,是固有免疫和适应性免疫之间的重要纽带。在 HIV-1 感染中,pDC 功能缺陷是最早观察到的免疫功能障碍之一。在此,我们回顾了 HIV-1 感染者中 pDC 的状况,以及这些细胞在发病机制中的潜在作用。我们首先回顾 pDC 的基本特性,然后讨论循环 pDC 数量和功能在早期和病毒血症 HIV-1 感染中的受损情况,以及可能导致 HIV 感染者中 pDC 耗竭的机制。此外,我们还回顾了慢性产生 IFN-α 的证据,这可能是通过 pDC 的慢性激活,是 HIV 感染中对免疫激活如此有害的关键。最后,我们讨论了 pDC 数量和功能平衡的重要性,以及使用绝对 pDC 计数和功能作为生物标志物的潜在价值,以及 HIV-1 感染者的 CD4(+)细胞计数和 VL。