• 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

细胞内 Casp8p41 含量与 CD4 T 细胞计数呈负相关。

Intracellular Casp8p41 content is inversely associated with CD4 T cell count.

机构信息

Division of Infectious Diseases, Mayo Clinic, Rochester, Minnesota 55905, USA.

出版信息

J Infect Dis. 2010 Aug 15;202(3):386-91. doi: 10.1086/653705.

DOI:10.1086/653705
PMID:20565257
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2906377/
Abstract

Casp8p41 is a protein fragment generated by cleavage of procaspase 8 by human immunodeficiency virus (HIV) protease. We measured Casp8p41 content in memory CD4 T cells and analyzed the association of Casp8p41 content with CD4 T cell count, cross-sectionally and longitudinally. Casp8p41 content was inversely correlated with CD4 T cell count, and change in Casp8p41 content was associated with absolute CD4 T cell count with change over time. Casp8p41 change was a better predictor of CD4 T cell count change than activated CD8 T cell percentage or viral load and was comparable to bacterial 16s DNA levels. This suggests that Casp8p41 is a relevant mediator of CD4 T cell death during HIV infection.

摘要

Casp8p41 是由人类免疫缺陷病毒 (HIV) 蛋白酶切割 procaspase 8 产生的蛋白片段。我们测量了记忆性 CD4 T 细胞中的 Casp8p41 含量,并分析了 Casp8p41 含量与 CD4 T 细胞计数的横断面和纵向关联。Casp8p41 含量与 CD4 T 细胞计数呈负相关,Casp8p41 含量的变化与绝对 CD4 T 细胞计数随时间的变化相关。与激活的 CD8 T 细胞百分比或病毒载量相比,Casp8p41 的变化能更好地预测 CD4 T 细胞计数的变化,与细菌 16sDNA 水平相当。这表明 Casp8p41 是 HIV 感染期间 CD4 T 细胞死亡的相关介质。

相似文献

1
Intracellular Casp8p41 content is inversely associated with CD4 T cell count.细胞内 Casp8p41 含量与 CD4 T 细胞计数呈负相关。
J Infect Dis. 2010 Aug 15;202(3):386-91. doi: 10.1086/653705.
2
Short communication: CD4 T cell declines occurring during suppressive antiretroviral therapy reflect continued production of Casp8p41.简短通讯:在抗逆转录病毒抑制疗法期间发生的CD4 T细胞减少反映了Casp8p41的持续产生。
AIDS Res Hum Retroviruses. 2014 May;30(5):476-9. doi: 10.1089/AID.2013.0243. Epub 2014 Feb 14.
3
Prime, Shock, and Kill: Priming CD4 T Cells from HIV Patients with a BCL-2 Antagonist before HIV Reactivation Reduces HIV Reservoir Size.启动、冲击与清除:在HIV重新激活前用BCL-2拮抗剂预处理HIV患者的CD4 T细胞可减小HIV储存库规模。
J Virol. 2016 Mar 28;90(8):4032-4048. doi: 10.1128/JVI.03179-15. Print 2016 Apr.
4
Casp8p41 expression in primary T cells induces a proinflammatory response.Casp8p41 在原代 T 细胞中的表达诱导促炎反应。
AIDS. 2010 Jun 1;24(9):1251-8. doi: 10.1097/QAD.0b013e3283389e90.
5
Human immunodeficiency virus type 1 protease cleaves procaspase 8 in vivo.1型人类免疫缺陷病毒蛋白酶在体内切割前半胱天冬酶8。
J Virol. 2007 Jul;81(13):6947-56. doi: 10.1128/JVI.02798-06. Epub 2007 Apr 18.
6
Programmed death-1 expression on CD4⁺ and CD8⁺ T cells in treated and untreated HIV disease.接受治疗和未接受治疗的HIV疾病中CD4⁺和CD8⁺ T细胞上程序性死亡-1的表达
AIDS. 2014 Jul 31;28(12):1749-58. doi: 10.1097/QAD.0000000000000314.
7
HIV Protease-Generated Casp8p41, When Bound and Inactivated by Bcl2, Is Degraded by the Proteasome.HIV 蛋白酶生成的 Casp8p41,当其与 Bcl2 结合并失活时,会被蛋白酶体降解。
J Virol. 2018 Jun 13;92(13). doi: 10.1128/JVI.00037-18. Print 2018 Jul 1.
8
[Characteristics of immunophenotypic alterations in 263 HIV/AIDS patients].[263例HIV/AIDS患者免疫表型改变的特征]
Zhonghua Yi Xue Za Zhi. 2006 Apr 11;86(14):965-9.
9
Combined Env- and Gag-specific T cell responses in relation to programmed death-1 receptor and CD4 T cell loss rates in human immunodeficiency virus-1 infection.在人类免疫缺陷病毒 1 感染中,与程序性死亡受体 1 和 CD4 T 细胞丢失率相关的联合 Env 和 gag 特异性 T 细胞反应。
Clin Exp Immunol. 2010 Aug;161(2):315-23. doi: 10.1111/j.1365-2249.2010.04179.x. Epub 2010 May 10.
10
Association of immune complexes and plasma viral load with CD4+ cell depletion, CD8+ DR+ and CD16+ cell counts in HIV+ hemophilia patients. Implications for the immunopathogenesis of HIV-induced CD4+ lymphocyte depletion.免疫复合物和血浆病毒载量与HIV阳性血友病患者CD4 +细胞耗竭、CD8 + DR +和CD16 +细胞计数的关系。对HIV诱导的CD4 +淋巴细胞耗竭免疫发病机制的影响。
Immunol Lett. 2001 Mar 1;76(2):69-78. doi: 10.1016/s0165-2478(01)00181-x.

引用本文的文献

1
Prime, shock and kill: BCL-2 inhibition for HIV cure.首要、冲击和杀伤:BCL-2 抑制用于 HIV 治愈。
Front Immunol. 2022 Oct 20;13:1033609. doi: 10.3389/fimmu.2022.1033609. eCollection 2022.
2
HIV Protease-Generated Casp8p41, When Bound and Inactivated by Bcl2, Is Degraded by the Proteasome.HIV 蛋白酶生成的 Casp8p41,当其与 Bcl2 结合并失活时,会被蛋白酶体降解。
J Virol. 2018 Jun 13;92(13). doi: 10.1128/JVI.00037-18. Print 2018 Jul 1.
3
Increasing procaspase 8 expression using repurposed drugs to induce HIV infected cell death in ex vivo patient cells.利用重新利用的药物增加前半胱天冬酶8的表达,以诱导离体患者细胞中受HIV感染的细胞死亡。
PLoS One. 2017 Jun 19;12(6):e0179327. doi: 10.1371/journal.pone.0179327. eCollection 2017.
4
Maintenance of the HIV Reservoir Is Antagonized by Selective BCL2 Inhibition.选择性抑制BCL2可对抗HIV储存库的维持。
J Virol. 2017 May 12;91(11). doi: 10.1128/JVI.00012-17. Print 2017 Jun 1.
5
Casp8p41: The Protean Mediator of Death in CD4 T-cells that Replicate HIV.Casp8p41:复制HIV的CD4 T细胞中多变的死亡介质。
J Cell Death. 2016 Sep 27;9:9-17. doi: 10.4137/JCD.S39872. eCollection 2016.
6
Prime, Shock, and Kill: Priming CD4 T Cells from HIV Patients with a BCL-2 Antagonist before HIV Reactivation Reduces HIV Reservoir Size.启动、冲击与清除:在HIV重新激活前用BCL-2拮抗剂预处理HIV患者的CD4 T细胞可减小HIV储存库规模。
J Virol. 2016 Mar 28;90(8):4032-4048. doi: 10.1128/JVI.03179-15. Print 2016 Apr.
7
Casp8p41 and HIV.半胱天冬酶8 p41与人类免疫缺陷病毒
Oncotarget. 2015 Sep 15;6(27):23042-3. doi: 10.18632/oncotarget.5238.
8
Making sense of how HIV kills infected CD4 T cells: implications for HIV cure.了解HIV如何杀死被感染的CD4 T细胞:对治愈HIV的意义。
Mol Cell Ther. 2014 Jul 3;2:20. doi: 10.1186/2052-8426-2-20. eCollection 2014.
9
Human immunodeficiency virus-1 (HIV-1)-mediated apoptosis: new therapeutic targets.人类免疫缺陷病毒1型(HIV-1)介导的细胞凋亡:新的治疗靶点。
Viruses. 2014 Aug 19;6(8):3181-227. doi: 10.3390/v6083181.
10
Short communication: CD4 T cell declines occurring during suppressive antiretroviral therapy reflect continued production of Casp8p41.简短通讯:在抗逆转录病毒抑制疗法期间发生的CD4 T细胞减少反映了Casp8p41的持续产生。
AIDS Res Hum Retroviruses. 2014 May;30(5):476-9. doi: 10.1089/AID.2013.0243. Epub 2014 Feb 14.

本文引用的文献

1
Plasma levels of bacterial DNA correlate with immune activation and the magnitude of immune restoration in persons with antiretroviral-treated HIV infection.接受抗逆转录病毒治疗的HIV感染者血浆中细菌DNA水平与免疫激活及免疫恢复程度相关。
J Infect Dis. 2009 Apr 15;199(8):1177-85. doi: 10.1086/597476.
2
HIV Protease Cleavage of Procaspase 8 is Necessary for Death of HIV-Infected Cells.HIV蛋白酶切割前半胱天冬酶8是HIV感染细胞死亡所必需的。
Open Virol J. 2008;2:1-7. doi: 10.2174/1874357900802010001.
3
Analysis of HIV Protease Killing Through Caspase 8 Reveals a Novel Interaction Between Caspase 8 and Mitochondria.通过半胱天冬酶8分析HIV蛋白酶杀伤作用揭示了半胱天冬酶8与线粒体之间的新型相互作用。
Open Virol J. 2007 Dec 27;1:39-46. doi: 10.2174/1874357900701010039.
4
Infected cell killing by HIV-1 protease promotes NF-kappaB dependent HIV-1 replication.HIV-1蛋白酶介导的受感染细胞杀伤促进NF-κB依赖性HIV-1复制。
PLoS One. 2008 May 7;3(5):e2112. doi: 10.1371/journal.pone.0002112.
5
Human immunodeficiency virus type 1 protease cleaves procaspase 8 in vivo.1型人类免疫缺陷病毒蛋白酶在体内切割前半胱天冬酶8。
J Virol. 2007 Jul;81(13):6947-56. doi: 10.1128/JVI.02798-06. Epub 2007 Apr 18.
6
Predictive value of plasma HIV RNA level on rate of CD4 T-cell decline in untreated HIV infection.血浆HIV RNA水平对未经治疗的HIV感染中CD4 T细胞下降速率的预测价值。
JAMA. 2006 Sep 27;296(12):1498-506. doi: 10.1001/jama.296.12.1498.
7
T-cell subsets that harbor human immunodeficiency virus (HIV) in vivo: implications for HIV pathogenesis.体内携带人类免疫缺陷病毒(HIV)的T细胞亚群:对HIV发病机制的影响
J Virol. 2004 Feb;78(3):1160-8. doi: 10.1128/jvi.78.3.1160-1168.2004.
8
Immune reconstitution is comparable in antiretroviral-naive subjects after 1 year of successful therapy with a nucleoside reverse-transcriptase inhibitor- or protease inhibitor-containing antiretroviral regimen.在使用含核苷逆转录酶抑制剂或蛋白酶抑制剂的抗逆转录病毒方案进行1年成功治疗后,初治抗逆转录病毒治疗的患者免疫重建情况相当。
J Infect Dis. 2003 Nov 15;188(10):1444-54. doi: 10.1086/379041. Epub 2003 Nov 13.
9
HIV-1 protease processes procaspase 8 to cause mitochondrial release of cytochrome c, caspase cleavage and nuclear fragmentation.HIV-1蛋白酶作用于procaspase 8,导致细胞色素c从线粒体释放、半胱天冬酶裂解及细胞核碎片化。
Cell Death Differ. 2002 Nov;9(11):1172-84. doi: 10.1038/sj.cdd.4401094.
10
Apoptosis of CD4+ and CD19+ cells during human immunodeficiency virus type 1 infection--correlation with clinical progression, viral load, and loss of humoral immunity.1型人类免疫缺陷病毒感染期间CD4+和CD19+细胞的凋亡——与临床进展、病毒载量及体液免疫丧失的相关性
Virology. 1997 Nov 24;238(2):180-8. doi: 10.1006/viro.1997.8790.