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AIDS Res Hum Retroviruses. 2012 Mar;28(3):295-8. doi: 10.1089/aid.2011.0003. Epub 2011 Jul 8.
2
IL-7 and the HIV Tat protein act synergistically to down-regulate CD127 expression on CD8 T cells.白细胞介素-7(IL-7)与人类免疫缺陷病毒反式激活蛋白(HIV Tat蛋白)协同作用,下调CD8 T细胞上CD127的表达。
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Progressive CD127 down-regulation correlates with increased apoptosis of CD8 T cells during chronic HIV-1 infection.在慢性HIV-1感染期间,CD127的逐渐下调与CD8 T细胞凋亡增加相关。
Eur J Immunol. 2009 May;39(5):1425-34. doi: 10.1002/eji.200839059.
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CD127 expression and regulation are altered in the memory CD8 T cells of HIV-infected patients--reversal by highly active anti-retroviral therapy (HAART).HIV感染患者记忆性CD8 T细胞中CD127的表达及调控发生改变——高效抗逆转录病毒疗法(HAART)可使其逆转
Clin Exp Immunol. 2006 Mar;143(3):398-403. doi: 10.1111/j.1365-2249.2006.03022.x.
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HIV infection of thymocytes inhibits IL-7 activity without altering CD127 expression.HIV 感染胸腺细胞会抑制 IL-7 活性,而不改变 CD127 的表达。
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[A cross-sectional study on the effect of virological response after HAART on subsets of T lymphocytes and expression of CD127 in pediatric AIDS patients with different viral loads].[高效抗逆转录病毒治疗后病毒学应答对不同病毒载量儿童艾滋病患者T淋巴细胞亚群及CD127表达影响的横断面研究]
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IL-7 induces sCD127 release and mCD127 downregulation in human CD8 T cells by distinct yet overlapping mechanisms, both of which are impaired in HIV infection.白细胞介素 7(IL-7)通过不同但重叠的机制诱导人 CD8 T 细胞释放可溶性 CD127(sCD127)并下调膜结合 CD127(mCD127),这两种机制在 HIV 感染中均受损。
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The N-Terminal Region of HIV-1 Tat Protein Binds CD127 in Human CD8 T Cells to Target the Receptor for Down Regulation Through Tat's Basic Region.HIV-1反式激活蛋白(Tat)的N端区域在人类CD8 T细胞中与CD127结合,通过Tat的碱性区域靶向该受体进行下调。
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Generalized Liver- and Blood-Derived CD8+ T-Cell Impairment in Response to Cytokines in Chronic Hepatitis C Virus Infection.慢性丙型肝炎病毒感染中,肝脏和血液来源的CD8 + T细胞对细胞因子应答的全身性损害
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1
IL-7-dependent STAT-5 activation and CD8+ T cell proliferation are impaired in HIV infection.HIV 感染会损害依赖 IL-7 的 STAT-5 激活和 CD8+ T 细胞增殖。
J Leukoc Biol. 2011 Apr;89(4):499-506. doi: 10.1189/jlb.0710430. Epub 2010 Dec 21.
2
Interleukin-4 downregulates CD127 expression and activity on human thymocytes and mature CD8+ T cells.白细胞介素-4 下调人胸腺细胞和成熟 CD8+T 细胞上的 CD127 表达和活性。
Eur J Immunol. 2010 May;40(5):1396-407. doi: 10.1002/eji.200940093.
3
IL-7 induces rapid clathrin-mediated internalization and JAK3-dependent degradation of IL-7Ralpha in T cells.白细胞介素-7(IL-7)诱导 T 细胞中 IL-7Rα 的网格蛋白介导的快速内化和 JAK3 依赖性降解。
Blood. 2010 Apr 22;115(16):3269-77. doi: 10.1182/blood-2009-10-246876. Epub 2010 Feb 26.
4
Dual mechanism of impairment of interleukin-7 (IL-7) responses in human immunodeficiency virus infection: decreased IL-7 binding and abnormal activation of the JAK/STAT5 pathway.人类免疫缺陷病毒感染中白细胞介素-7(IL-7)反应受损的双重机制:IL-7 结合减少和 JAK/STAT5 途径的异常激活。
J Virol. 2010 Jan;84(1):96-108. doi: 10.1128/JVI.01475-09.
5
IL-7 decreases IL-7 receptor alpha (CD127) expression and induces the shedding of CD127 by human CD8+ T cells.白细胞介素-7可降低白细胞介素-7受体α(CD127)的表达,并诱导人CD8 + T细胞使其CD127脱落。
Int Immunol. 2007 Dec;19(12):1329-39. doi: 10.1093/intimm/dxm102. Epub 2007 Oct 22.
6
Loss of IL-7 receptor alpha-chain (CD127) expression in acute HCV infection associated with viral persistence.急性丙型肝炎病毒感染中白细胞介素-7受体α链(CD127)表达缺失与病毒持续存在相关。
Hepatology. 2006 Nov;44(5):1098-109. doi: 10.1002/hep.21365.
7
Interleukin-7 receptor expression on CD8 T-cells is downregulated by the HIV Tat protein.白细胞介素-7受体在CD8 T细胞上的表达被HIV反式激活蛋白下调。
J Acquir Immune Defic Syndr. 2006 Nov 1;43(3):257-69. doi: 10.1097/01.qai.0000230319.78288.f4.
8
CD127 expression and regulation are altered in the memory CD8 T cells of HIV-infected patients--reversal by highly active anti-retroviral therapy (HAART).HIV感染患者记忆性CD8 T细胞中CD127的表达及调控发生改变——高效抗逆转录病毒疗法(HAART)可使其逆转
Clin Exp Immunol. 2006 Mar;143(3):398-403. doi: 10.1111/j.1365-2249.2006.03022.x.
9
Increased plasma interleukin-7 level correlates with decreased CD127 and Increased CD132 extracellular expression on T cell subsets in patients with HIV-1 infection.在HIV-1感染患者中,血浆白细胞介素-7水平升高与T细胞亚群上CD127表达降低及CD132细胞外表达增加相关。
J Infect Dis. 2006 Feb 15;193(4):505-14. doi: 10.1086/499309. Epub 2006 Jan 17.
10
IL-7Ralpha expression on CD4+ T lymphocytes decreases with HIV disease progression and inversely correlates with immune activation.CD4+ T淋巴细胞上的白细胞介素-7受体α(IL-7Rα)表达随着HIV疾病进展而降低,且与免疫激活呈负相关。
Eur J Immunol. 2006 Feb;36(2):336-44. doi: 10.1002/eji.200535111.

体外1型人类免疫缺陷病毒感染间接改变CD8(+) T细胞上CD127的表达。

In vitro HIV Type 1 infection indirectly alters CD127 expression on CD8(+) T cells.

作者信息

Vranjkovic Agatha, Crawley Angela M, Angel Jonathan B

机构信息

Ottawa Hospital Research Institute, Ontario, K1H 8L6, Canada.

出版信息

AIDS Res Hum Retroviruses. 2012 Mar;28(3):295-8. doi: 10.1089/aid.2011.0003. Epub 2011 Jul 8.

DOI:10.1089/aid.2011.0003
PMID:21740271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3292746/
Abstract

Decreased expression of interleukin (IL)-7 receptor α (CD127) on CD8(+) T cells in progressive HIV disease suggests a role for CD127 regulation in HIV immunopathogenesis. The direct effect of HIV on CD127 expression has not been explored to explain these in vivo findings. Peripheral blood mononuclear cells (PBMCs) or isolated CD8(+) T cells from healthy individuals were cultured with either X4 (HIV-1(IIIB)), R5 (HIV-1(BaL)), dual tropic (HIV-1(CS204)), or replication-incompetent (HIV(8E5)) strains of HIV. Both X4 and R5 strains transiently decreased CD127 expression on CD8(+) T cells in PBMC cultures but had no effect on isolated CD8(+) T cell cultures. Isolated CD8(+) T cells exposed to either (1) PBMCs incubated with HIV and cultured in a transwell or (2) supernatants from PBMCs incubated with HIV resulted in decreased CD127 expression. Under no conditions did the replication-incompetent HIV strain affect CD127 expression. As observed in vivo, infection of PBMCs with HIV in vitro results in the downregulation of CD127 surface expression on CD8(+) T cells. Collectively, these data indicate that soluble factor(s) released as a result of HIV infection regulate CD127 expression. Further elucidation of the mechanism(s) of CD127 downregulation will provide important insights into the immunopathogenesis of HIV disease.

摘要

在进展性HIV疾病中,CD8(+) T细胞上白细胞介素(IL)-7受体α(CD127)的表达降低,提示CD127调节在HIV免疫发病机制中发挥作用。尚未探究HIV对CD127表达的直接影响,以解释这些体内研究结果。将来自健康个体的外周血单核细胞(PBMC)或分离的CD8(+) T细胞与X4(HIV-1(IIIB))、R5(HIV-1(BaL))、双嗜性(HIV-1(CS204))或无复制能力(HIV(8E5))的HIV毒株一起培养。X4和R5毒株均可使PBMC培养物中CD8(+) T细胞上的CD127表达短暂降低,但对分离的CD8(+) T细胞培养物无影响。分离的CD8(+) T细胞暴露于以下两种情况均可导致CD127表达降低:(1)与HIV一起孵育并在Transwell中培养的PBMC;(2)与HIV一起孵育的PBMC的上清液。在任何情况下,无复制能力的HIV毒株均不影响CD127表达。正如在体内观察到的那样,体外HIV感染PBMC会导致CD8(+) T细胞上CD127表面表达下调。总的来说,这些数据表明,HIV感染释放的可溶性因子调节CD127表达。进一步阐明CD127下调的机制将为深入了解HIV疾病的免疫发病机制提供重要线索。