• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

尽管循环中的HIV水平较低,但CD4 T细胞计数仍低:对接受抗逆转录病毒治疗反应不一致的HIV-1感染患者与未经治疗的晚期HIV-2疾病患者进行比较的见解。

Low CD4 T-cell counts despite low levels of circulating HIV: insights from the comparison of HIV-1 infected patients with a discordant response to antiretroviral therapy to patients with untreated advanced HIV-2 disease.

作者信息

Albuquerque Adriana S, Foxall Russell B, Cortesão Catarina S, Soares Rui S, Doroana Manuela, Ribeiro Alice, Lucas Margarida, Antunes Francisco, Victorino Rui M M, Sousa Ana E

机构信息

Unidade de Imunologia Clínica, Instituto de Medicina Molecular, Faculdade de Medicina de Lisboa, Av Prof Egas Moniz, 1649-028, Lisboa, Portugal.

出版信息

Clin Immunol. 2007 Oct;125(1):67-75. doi: 10.1016/j.clim.2007.07.001. Epub 2007 Aug 9.

DOI:10.1016/j.clim.2007.07.001
PMID:17692571
Abstract

A significant proportion of HIV-1+ patients with suppression of viremia under antiretroviral therapy fail to recover CD4(+) T-cell counts (ART-Discordants). Similarly, untreated HIV-2+ patients can also exhibit major CD4 depletion in spite of undetectable viremia. We characterize here the immunological disturbances associated with major CD4-lymphopenia in these two scenarios as compared to untreated viremic HIV-1+ patients with similar CD4-lymphopenia and HIV-1+ patients with successful immunological and virological responses under ART. Low CD4 counts were associated with major naive CD4 and CD8 depletion, irrespective of type of infection or ART-exposure. However, ART-Discordants exhibited lower levels of T-cell activation as compared to both untreated HIV-2 and HIV-1 cohorts, and a less marked increase in circulating IL-7 despite similar CD4 depletion. Nevertheless, ART-Discordants showed a preserved Bcl-2 expression, suggesting increased IL-7 consumption, which in conjunction with the relatively lower T-cell activation may contribute to their CD4 count stability and low rate of opportunistic infections.

摘要

相当一部分接受抗逆转录病毒治疗后病毒血症得到抑制的HIV-1阳性患者未能恢复CD4(+) T细胞计数(抗逆转录病毒治疗反应不一致者)。同样,未经治疗的HIV-2阳性患者尽管病毒血症检测不到,但也可能出现严重的CD4细胞耗竭。与未经治疗、病毒血症阳性且CD4淋巴细胞减少情况相似的HIV-1阳性患者以及接受抗逆转录病毒治疗后免疫和病毒学反应成功的HIV-1阳性患者相比,我们在此描述了这两种情况下与严重CD4淋巴细胞减少相关的免疫紊乱。无论感染类型或是否接受抗逆转录病毒治疗,低CD4计数都与主要的初始CD4和CD8细胞耗竭有关。然而,与未经治疗的HIV-2和HIV-1队列相比,抗逆转录病毒治疗反应不一致者的T细胞活化水平较低,尽管CD4细胞耗竭情况相似,但循环IL-7的增加不太明显。尽管如此,抗逆转录病毒治疗反应不一致者的Bcl-2表达保持不变,提示IL-7消耗增加,这与相对较低的T细胞活化可能共同导致其CD4计数稳定以及机会性感染发生率较低。

相似文献

1
Low CD4 T-cell counts despite low levels of circulating HIV: insights from the comparison of HIV-1 infected patients with a discordant response to antiretroviral therapy to patients with untreated advanced HIV-2 disease.尽管循环中的HIV水平较低,但CD4 T细胞计数仍低:对接受抗逆转录病毒治疗反应不一致的HIV-1感染患者与未经治疗的晚期HIV-2疾病患者进行比较的见解。
Clin Immunol. 2007 Oct;125(1):67-75. doi: 10.1016/j.clim.2007.07.001. Epub 2007 Aug 9.
2
Determinants of CD4+ T cell recovery during suppressive antiretroviral therapy: association of immune activation, T cell maturation markers, and cellular HIV-1 DNA.抑制性抗逆转录病毒治疗期间CD4 + T细胞恢复的决定因素:免疫激活、T细胞成熟标志物与细胞内HIV-1 DNA的关联
J Infect Dis. 2006 Jul 1;194(1):29-37. doi: 10.1086/504718. Epub 2006 May 18.
3
HIV-1-infected children on HAART: immunologic features of three different levels of viral suppression.接受高效抗逆转录病毒治疗的HIV-1感染儿童:三种不同病毒抑制水平的免疫学特征。
Cytometry B Clin Cytom. 2007 Jan 15;72(1):14-21. doi: 10.1002/cyto.b.20152.
4
T cell activation in HIV-seropositive Ugandans: differential associations with viral load, CD4+ T cell depletion, and coinfection.乌干达艾滋病毒血清阳性者的T细胞激活:与病毒载量、CD4 + T细胞耗竭及合并感染的不同关联
J Infect Dis. 2005 Mar 1;191(5):694-701. doi: 10.1086/427516. Epub 2005 Jan 31.
5
Similar changes in plasmacytoid dendritic cell and CD4 T-cell counts during primary HIV-1 infection and treatment.原发性HIV-1感染及治疗期间浆细胞样树突状细胞和CD4 T细胞计数的类似变化。
AIDS. 2006 Jun 12;20(9):1247-52. doi: 10.1097/01.aids.0000232231.34253.bd.
6
Proportions of circulating T cells with a regulatory cell phenotype increase with HIV-associated immune activation and remain high on antiretroviral therapy.具有调节性细胞表型的循环T细胞比例随HIV相关免疫激活而增加,并在抗逆转录病毒治疗期间保持高位。
AIDS. 2007 Jul 31;21(12):1525-34. doi: 10.1097/QAD.0b013e32825eab8b.
7
Antiretroviral therapy-induced dominant interleukin-2 HIV-1 Gag CD4+ T cell response: evidence of functional recovery of HIV-1-specific CD4+ T cells.抗逆转录病毒疗法诱导的占主导地位的白细胞介素-2 HIV-1 Gag CD4+ T 细胞反应:HIV-1 特异性 CD4+ T 细胞功能恢复的证据。
Scand J Immunol. 2011 Mar;73(3):256-65. doi: 10.1111/j.1365-3083.2010.02502.x.
8
Loss of correlation between HIV viral load and CD4+ T-cell counts in HIV/HTLV-1 co-infection in treatment naive Mozambican patients.初治莫桑比克患者HIV/HTLV-1合并感染时,HIV病毒载量与CD4+ T细胞计数之间的相关性丧失。
Int J STD AIDS. 2009 Dec;20(12):863-8. doi: 10.1258/ijsa.2008.008401.
9
Biological determinants of immune reconstitution in HIV-infected patients receiving antiretroviral therapy: the role of interleukin 7 and interleukin 7 receptor α and microbial translocation.抗逆转录病毒治疗的 HIV 感染患者免疫重建的生物学决定因素:白细胞介素 7 和白细胞介素 7 受体 α 及微生物易位的作用。
J Infect Dis. 2010 Oct 15;202(8):1254-64. doi: 10.1086/656369.
10
Altered clonogenic capability and stromal cell function characterize bone marrow of HIV-infected subjects with low CD4+ T cell counts despite viral suppression during HAART.尽管在高效抗逆转录病毒治疗(HAART)期间病毒得到抑制,但克隆形成能力和基质细胞功能的改变是CD4 + T细胞计数低的HIV感染受试者骨髓的特征。
Clin Infect Dis. 2008 Jun 15;46(12):1902-10. doi: 10.1086/588480.

引用本文的文献

1
HIV Nef and Antiretroviral Therapy Have an Inhibitory Effect on Autophagy in Human Astrocytes that May Contribute to HIV-Associated Neurocognitive Disorders.HIV Nef 和抗逆转录病毒疗法对人星形胶质细胞自噬具有抑制作用,可能导致与 HIV 相关的神经认知障碍。
Cells. 2020 Jun 9;9(6):1426. doi: 10.3390/cells9061426.
2
Major CD4 T-Cell Depletion and Immune Senescence in a Patient with Chronic Granulomatous Disease.一名慢性肉芽肿病患者出现主要CD4 T细胞耗竭和免疫衰老
Front Immunol. 2017 May 11;8:543. doi: 10.3389/fimmu.2017.00543. eCollection 2017.