• 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

CD8 + T淋巴细胞选择在猴免疫缺陷病毒序列变异中起主导作用。

A dominant role for CD8+-T-lymphocyte selection in simian immunodeficiency virus sequence variation.

作者信息

O'Connor David H, McDermott Adrian B, Krebs Kendall C, Dodds Elizabeth J, Miller Jacqueline E, Gonzalez Edna J, Jacoby Timothy J, Yant Levi, Piontkivska Helen, Pantophlet Ralph, Burton Dennis R, Rehrauer William M, Wilson Nancy, Hughes Austin L, Watkins David I

机构信息

Wisconsin Primate Research Center, Department of Pathology, Laboratoty of Medicine, University of Wisconsin, 1300 University Ave., Madison, WI 53706, USA.

出版信息

J Virol. 2004 Dec;78(24):14012-22. doi: 10.1128/JVI.78.24.14012-14022.2004.

DOI:10.1128/JVI.78.24.14012-14022.2004
PMID:15564508
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC533930/
Abstract

CD8(+) T lymphocytes (CD8-TL) select viral escape variants in both human immunodeficiency virus and simian immunodeficiency virus (SIV) infections. The frequency of CD8-TL viral escape as well as the contribution of escape to overall virus diversification has not been assessed. We quantified CD8-TL selection in SIV infections by sequencing viral genomes from 35 SIVmac239-infected animals at the time of euthanasia. Here we show that positive selection for sequences encoding 46 known CD8-TL epitopes is comparable to the positive selection observed for the variable loops of env. We also found that >60% of viral variation outside of the viral envelope occurs within recognized CD8-TL epitopes. Therefore, we conclude that CD8-TL selection is the dominant cause of SIV diversification outside of the envelope.

摘要

CD8(+) T淋巴细胞(CD8-TL)在人类免疫缺陷病毒和猴免疫缺陷病毒(SIV)感染中均会选择病毒逃逸变体。尚未评估CD8-TL病毒逃逸的频率以及逃逸对整体病毒多样性的贡献。我们通过在安乐死时对35只感染SIVmac239的动物的病毒基因组进行测序,量化了SIV感染中CD8-TL的选择。在此我们表明,对编码46个已知CD8-TL表位的序列的阳性选择与对env可变环观察到的阳性选择相当。我们还发现,病毒包膜外>60%的病毒变异发生在公认的CD8-TL表位内。因此,我们得出结论,CD8-TL选择是包膜外SIV多样性的主要原因。

相似文献

1
A dominant role for CD8+-T-lymphocyte selection in simian immunodeficiency virus sequence variation.CD8 + T淋巴细胞选择在猴免疫缺陷病毒序列变异中起主导作用。
J Virol. 2004 Dec;78(24):14012-22. doi: 10.1128/JVI.78.24.14012-14022.2004.
2
Ultradeep pyrosequencing detects complex patterns of CD8+ T-lymphocyte escape in simian immunodeficiency virus-infected macaques.超深度焦磷酸测序检测猿猴免疫缺陷病毒感染猕猴中CD8 + T淋巴细胞逃逸的复杂模式。
J Virol. 2009 Aug;83(16):8247-53. doi: 10.1128/JVI.00897-09. Epub 2009 Jun 10.
3
Tertiary mutations stabilize CD8+ T lymphocyte escape-associated compensatory mutations following transmission of simian immunodeficiency virus.在猴免疫缺陷病毒传播后,三级突变稳定了与 CD8+T 淋巴细胞逃逸相关的补偿性突变。
J Virol. 2014 Mar;88(6):3598-604. doi: 10.1128/JVI.03304-13. Epub 2013 Dec 26.
4
SIV genome-wide pyrosequencing provides a comprehensive and unbiased view of variation within and outside CD8 T lymphocyte epitopes.SIV 全基因组焦磷酸测序为 CD8 T 淋巴细胞表位内外的变异提供了全面、无偏的视角。
PLoS One. 2012;7(10):e47818. doi: 10.1371/journal.pone.0047818. Epub 2012 Oct 24.
5
Maintenance of AP-2-Dependent Functional Activities of Nef Restricts Pathways of Immune Escape from CD8 T Lymphocyte Responses.Nef依赖AP-2的功能活性的维持限制了从CD8 T淋巴细胞反应中免疫逃逸的途径。
J Virol. 2018 Feb 12;92(5). doi: 10.1128/JVI.01822-17. Print 2018 Mar 1.
6
Comprehensive immunological evaluation reveals surprisingly few differences between elite controller and progressor Mamu-B*17-positive simian immunodeficiency virus-infected rhesus macaques.全面的免疫学评估显示,在精英控制者和疾病进展者中,感染猴免疫缺陷病毒且Mamu - B*17呈阳性的恒河猴之间的差异出奇地少。
J Virol. 2008 Jun;82(11):5245-54. doi: 10.1128/JVI.00292-08. Epub 2008 Apr 2.
7
Acute phase CD8+ T lymphocytes against alternate reading frame epitopes select for rapid viral escape during SIV infection.急性相 CD8+ T 淋巴细胞针对交替阅读框表位选择在 SIV 感染期间快速发生病毒逃逸。
PLoS One. 2013 May 6;8(5):e61383. doi: 10.1371/journal.pone.0061383. Print 2013.
8
Patterns of CD8+ immunodominance may influence the ability of Mamu-B*08-positive macaques to naturally control simian immunodeficiency virus SIVmac239 replication.CD8 +免疫显性模式可能会影响Mamu - B*08阳性猕猴自然控制猿猴免疫缺陷病毒SIVmac239复制的能力。
J Virol. 2008 Feb;82(4):1723-38. doi: 10.1128/JVI.02084-07. Epub 2007 Dec 5.
9
Conditional Immune Escape during Chronic Simian Immunodeficiency Virus Infection.慢性猿猴免疫缺陷病毒感染期间的条件性免疫逃逸
J Virol. 2015 Oct 21;90(1):545-52. doi: 10.1128/JVI.02587-15. Print 2016 Jan 1.
10
Epitope-specific CD8+ T lymphocytes cross-recognize mutant simian immunodeficiency virus (SIV) sequences but fail to contain very early evolution and eventual fixation of epitope escape mutations during SIV infection.表位特异性 CD8+ T 淋巴细胞可交叉识别突变的猴免疫缺陷病毒 (SIV) 序列,但无法在 SIV 感染过程中阻止早期进化和最终固定表位逃逸突变。
J Virol. 2011 Apr;85(8):3746-57. doi: 10.1128/JVI.02420-10. Epub 2011 Feb 9.

引用本文的文献

1
Preferential selection of viral escape mutants by CD8+ T cell 'sieving' of SIV reactivation from latency.CD8+ T 细胞“筛选”潜伏状态下 SIV 的再激活,有利于病毒逃逸突变体的选择。
PLoS Pathog. 2023 Nov 30;19(11):e1011755. doi: 10.1371/journal.ppat.1011755. eCollection 2023 Nov.
2
APOBEC3G Regulation of the Evolutionary Race Between Adaptive Immunity and Viral Immune Escape Is Deeply Imprinted in the HIV Genome.APOBEC3G 对适应性免疫与病毒免疫逃逸之间进化竞争的调控在 HIV 基因组中留下了深刻的印记。
Front Immunol. 2019 Jan 11;9:3032. doi: 10.3389/fimmu.2018.03032. eCollection 2018.
3
Maintenance of AP-2-Dependent Functional Activities of Nef Restricts Pathways of Immune Escape from CD8 T Lymphocyte Responses.Nef依赖AP-2的功能活性的维持限制了从CD8 T淋巴细胞反应中免疫逃逸的途径。
J Virol. 2018 Feb 12;92(5). doi: 10.1128/JVI.01822-17. Print 2018 Mar 1.
4
Acute Viral Escape Selectively Impairs Nef-Mediated Major Histocompatibility Complex Class I Downmodulation and Increases Susceptibility to Antiviral T Cells.急性病毒逃逸选择性损害Nef介导的主要组织相容性复合体I类下调并增加对抗病毒T细胞的易感性。
J Virol. 2015 Dec 4;90(4):2119-26. doi: 10.1128/JVI.01975-15. Print 2016 Feb 15.
5
Noncytolytic CD8+ Cell Mediated Antiviral Response Represents a Strong Element in the Immune Response of Simian Immunodeficiency Virus-Infected Long-Term Non-Progressing Rhesus Macaques.非细胞溶解性CD8 +细胞介导的抗病毒反应是猿猴免疫缺陷病毒感染的长期不进展恒河猴免疫反应中的一个重要因素。
PLoS One. 2015 Nov 9;10(11):e0142086. doi: 10.1371/journal.pone.0142086. eCollection 2015.
6
A Novel Codon-optimized SIV Gag-pol Immunogen for Gene-based Vaccination.一种用于基因疫苗接种的新型密码子优化的猴免疫缺陷病毒Gag-pol免疫原。
Virol Rep. 2015 Dec 1;5:47-55. doi: 10.1016/j.virep.2015.03.002. Epub 2015 Mar 10.
7
Conditional Immune Escape during Chronic Simian Immunodeficiency Virus Infection.慢性猿猴免疫缺陷病毒感染期间的条件性免疫逃逸
J Virol. 2015 Oct 21;90(1):545-52. doi: 10.1128/JVI.02587-15. Print 2016 Jan 1.
8
Tertiary mutations stabilize CD8+ T lymphocyte escape-associated compensatory mutations following transmission of simian immunodeficiency virus.在猴免疫缺陷病毒传播后,三级突变稳定了与 CD8+T 淋巴细胞逃逸相关的补偿性突变。
J Virol. 2014 Mar;88(6):3598-604. doi: 10.1128/JVI.03304-13. Epub 2013 Dec 26.
9
Acute phase CD8+ T lymphocytes against alternate reading frame epitopes select for rapid viral escape during SIV infection.急性相 CD8+ T 淋巴细胞针对交替阅读框表位选择在 SIV 感染期间快速发生病毒逃逸。
PLoS One. 2013 May 6;8(5):e61383. doi: 10.1371/journal.pone.0061383. Print 2013.
10
Hepatitis C virus adaptation to T-cell immune pressure.丙型肝炎病毒对T细胞免疫压力的适应性
ScientificWorldJournal. 2013;2013:673240. doi: 10.1155/2013/673240. Epub 2013 Mar 11.

本文引用的文献

1
Identification of seventeen new simian immunodeficiency virus-derived CD8+ T cell epitopes restricted by the high frequency molecule, Mamu-A*02, and potential escape from CTL recognition.鉴定出17个由高频分子Mamu - A*02限制的新的猿猴免疫缺陷病毒衍生的CD8 + T细胞表位以及潜在的CTL识别逃逸情况。
J Immunol. 2004 Oct 15;173(8):5064-76. doi: 10.4049/jimmunol.173.8.5064.
2
Immune selection for altered antigen processing leads to cytotoxic T lymphocyte escape in chronic HIV-1 infection.针对抗原加工改变的免疫选择导致慢性HIV-1感染中细胞毒性T淋巴细胞逃逸。
J Exp Med. 2004 Apr 5;199(7):905-15. doi: 10.1084/jem.20031982.
3
Repeated low-dose mucosal simian immunodeficiency virus SIVmac239 challenge results in the same viral and immunological kinetics as high-dose challenge: a model for the evaluation of vaccine efficacy in nonhuman primates.重复低剂量黏膜猴免疫缺陷病毒SIVmac239攻击导致与高剂量攻击相同的病毒和免疫动力学:一种用于评估非人灵长类动物疫苗效力的模型
J Virol. 2004 Mar;78(6):3140-4. doi: 10.1128/jvi.78.6.3140-3144.2004.
4
Extraepitopic compensatory substitutions partially restore fitness to simian immunodeficiency virus variants that escape from an immunodominant cytotoxic-T-lymphocyte response.表位外补偿性替换可部分恢复从免疫显性细胞毒性T淋巴细胞应答中逃逸的猿猴免疫缺陷病毒变体的适应性。
J Virol. 2004 Mar;78(5):2581-5. doi: 10.1128/jvi.78.5.2581-2585.2004.
5
Removal of N-linked glycosylation sites in the V1 region of simian immunodeficiency virus gp120 results in redirection of B-cell responses to V3.去除猿猴免疫缺陷病毒gp120 V1区域的N-连接糖基化位点会导致B细胞反应重定向至V3区域。
J Virol. 2004 Feb;78(3):1525-39. doi: 10.1128/jvi.78.3.1525-1539.2004.
6
Impaired processing and presentation of cytotoxic-T-lymphocyte (CTL) epitopes are major escape mechanisms from CTL immune pressure in human immunodeficiency virus type 1 infection.细胞毒性T淋巴细胞(CTL)表位的加工与呈递受损是1型人类免疫缺陷病毒感染中CTL免疫压力主要的逃逸机制。
J Virol. 2004 Feb;78(3):1324-32. doi: 10.1128/jvi.78.3.1324-1332.2004.
7
Persistent recognition of autologous virus by high-avidity CD8 T cells in chronic, progressive human immunodeficiency virus type 1 infection.在慢性进行性1型人类免疫缺陷病毒感染中,高亲和力CD8 T细胞对自体病毒的持续识别。
J Virol. 2004 Jan;78(2):630-41. doi: 10.1128/jvi.78.2.630-641.2004.
8
Simian-human immunodeficiency virus escape from cytotoxic T-lymphocyte recognition at a structurally constrained epitope.猿猴-人类免疫缺陷病毒在结构受限表位处逃避细胞毒性T淋巴细胞识别。
J Virol. 2003 Dec;77(23):12572-8. doi: 10.1128/jvi.77.23.12572-12578.2003.
9
Major histocompatibility complex class I alleles associated with slow simian immunodeficiency virus disease progression bind epitopes recognized by dominant acute-phase cytotoxic-T-lymphocyte responses.与猿猴免疫缺陷病毒疾病进展缓慢相关的主要组织相容性复合体I类等位基因结合优势急性期细胞毒性T淋巴细胞反应所识别的表位。
J Virol. 2003 Aug;77(16):9029-40. doi: 10.1128/jvi.77.16.9029-9040.2003.
10
Viral escape from dominant simian immunodeficiency virus epitope-specific cytotoxic T lymphocytes in DNA-vaccinated rhesus monkeys.在接种DNA疫苗的恒河猴中,病毒从主要的猿猴免疫缺陷病毒表位特异性细胞毒性T淋巴细胞中逃逸。
J Virol. 2003 Jul;77(13):7367-75. doi: 10.1128/jvi.77.13.7367-7375.2003.