Suppr超能文献

一种被CD8 + T细胞识别的源自SV40 VP1的表位可被HLA - A*0201自然加工和呈递,并与人多瘤病毒决定簇发生交叉反应。

An SV40 VP1-derived epitope recognized by CD8+ T cells is naturally processed and presented by HLA-A*0201 and cross-reactive with human polyomavirus determinants.

作者信息

Tagaram Hephzibah Rani S, Watson Alan M, Lemonnier Francois A, Staveley-O'Carroll Kevin, Tevethia Satvir S, Schell Todd D

机构信息

Department of Surgery, The Pennsylvania State University College of Medicine, Hershey, PA 17033, USA.

出版信息

Virology. 2008 Jun 20;376(1):183-90. doi: 10.1016/j.virol.2008.02.033. Epub 2008 Apr 10.

Abstract

The CD8+ T cell responses directed toward the VP1 antigens of human polyomaviruses JC and BK recently were shown to be cross-reactive. Two HLA-A0201-restricted determinants from each virus have been defined and include JCp100-108 (ILMWEAVTL) and BKp108-116 (LLMWEAVTV) as well as JCp36-44 (SITEVECFL) and BKp44-52 (AITEVECFL). We asked whether VP1 from the related SV40 contains similar HLA-A0201-restricted determinants. In this study, we demonstrate that CD8+ T cells specific for SV40 VP1 p110-118 (ILMWEAVTV), but not p46-54 (SFTEVECFL), can be induced in HLA-A0201-transgenic mice and that these CD8+ T cells cross-react with the corresponding determinants from JC and BK virus. The SV40 p110 determinant was found to be processed and presented in SV40-infected cells. These results indicate that the JCp36/BKp44 determinants are distinctive for the human polyomaviruses while the JCp100/BKp108/SVp110 determinants are shared by all three viruses, providing a target for CD8+ T cell cross-reactivity.

摘要

最近研究表明,针对人多瘤病毒JC和BK的VP1抗原的CD8 + T细胞反应具有交叉反应性。已确定了每种病毒的两个HLA - A0201限制性决定簇,包括JCp100 - 108(ILMWEAVTL)和BKp108 - 116(LLMWEAVTV)以及JCp36 - 44(SITEVECFL)和BKp44 - 52(AITEVECFL)。我们询问相关的SV40病毒的VP1是否含有类似的HLA - A0201限制性决定簇。在本研究中,我们证明在HLA - A0201转基因小鼠中可诱导出对SV40 VP1 p110 - 118(ILMWEAVTV)特异的CD8 + T细胞,而对p46 - 54(SFTEVECFL)无反应,并且这些CD8 + T细胞与JC和BK病毒的相应决定簇发生交叉反应。发现SV40 p110决定簇在SV40感染的细胞中被加工并呈递。这些结果表明,JCp36 / BKp44决定簇是人多瘤病毒所特有的,而JCp100 / BKp108 / SVp110决定簇为三种病毒所共有,为CD8 + T细胞交叉反应提供了一个靶点。

相似文献

8
HLA-A01-, -A03-, and -A024-binding nanomeric epitopes in polyomavirus BK large T antigen.
Hum Immunol. 2009 Sep;70(9):722-8. doi: 10.1016/j.humimm.2009.05.003. Epub 2009 May 14.

引用本文的文献

1
Schweinfurthin induces ICD without ER stress and caspase activation.
Oncoimmunology. 2022 Aug 3;11(1):2104551. doi: 10.1080/2162402X.2022.2104551. eCollection 2022.
2
BK Polyomavirus: Clinical Aspects, Immune Regulation, and Emerging Therapies.
Clin Microbiol Rev. 2017 Apr;30(2):503-528. doi: 10.1128/CMR.00074-16.
3
Phenotypic and functional characterization of circulating polyomavirus BK VP1-specific CD8+ T cells in healthy adults.
J Virol. 2013 Sep;87(18):10263-72. doi: 10.1128/JVI.01540-13. Epub 2013 Jul 17.
5
HLA-A01-, -A03-, and -A024-binding nanomeric epitopes in polyomavirus BK large T antigen.
Hum Immunol. 2009 Sep;70(9):722-8. doi: 10.1016/j.humimm.2009.05.003. Epub 2009 May 14.

本文引用的文献

1
SV40 and human cancer: a review of recent data.
Int J Cancer. 2007 Jan 15;120(2):215-23. doi: 10.1002/ijc.22425.
3
BK virus infection in transplant recipients: an overview and update.
Am J Transplant. 2006 Sep;6(9):2000-5. doi: 10.1111/j.1600-6143.2006.01403.x. Epub 2006 Jun 9.
7
Emergent human pathogen simian virus 40 and its role in cancer.
Clin Microbiol Rev. 2004 Jul;17(3):495-508, table of contents. doi: 10.1128/CMR.17.3.495-508.2004.
10
Development of tumors in hamsters inoculated in the neonatal period with vacuolating virus, SV-40.
Proc Soc Exp Biol Med. 1962 Mar;109:649-60. doi: 10.3181/00379727-109-27298.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验