• 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

麻疹病毒经甲醛灭活后,可消除核蛋白依赖CD46向小鼠I类限制性细胞毒性T淋巴细胞的呈递,但对II类限制性辅助性T细胞的呈递无影响。

Formaldehyde inactivation of measles virus abolishes CD46-dependent presentation of nucleoprotein to murine class I-restricted CTLs but not to class II-restricted helper T cells.

作者信息

Cardoso A I, Beauverger P, Gerlier D, Wild T F, Rabourdin-Combe C

机构信息

CNRS, UMR 49, Ecole Normale Supérieure de Lyon, France.

出版信息

Virology. 1995 Sep 10;212(1):255-8. doi: 10.1006/viro.1995.1479.

DOI:10.1006/viro.1995.1479
PMID:7676641
Abstract

To induce an MHC-restricted specific CTL or Th response, an antigen must be delivered into the appropriate cellular compartment. We explored the role of CD46 in the presentation of measles virus (MV) nucleoprotein (NP) to murine NP-specific and MHC Class I-restricted polyclonal CTLs and the effect of inactivating MV by uv or formaldehyde. CD46(-)- and CD46(+)-transfected murine cells were used as target cells. After MV infection, only the targets which expressed CD46 were lysed by NP-specific class I-restricted CTLs. When MV was uv-inactivated, NP presentation by MHC class I molecules was retained but could be blocked by fusion inhibitors which block virus cell entry. When MV was inactivated with formaldehyde, NP was no longer presented by MHC class I molecules, although it was still presented by MHC class II molecules to a NP-specific class II-restricted T cell hybridoma. These data show that MV binding to the CD46 molecule is a prerequisite for virus-to-cell fusion and that cytosolic delivery of NP is necessary for presentation by class I molecules. Moreover, formaldehyde inactivation of virus induces the loss of class I-restricted presentation of NP due to selective abrogation of fusion and cytosolic delivery of NP.

摘要

为诱导MHC限制的特异性CTL或Th应答,抗原必须被递送至适当的细胞区室。我们探究了CD46在将麻疹病毒(MV)核蛋白(NP)呈递给鼠NP特异性且MHC I类限制的多克隆CTL中的作用,以及紫外线或甲醛使MV失活的影响。用CD46(-)和CD46(+)转染的鼠细胞作为靶细胞。MV感染后,只有表达CD46的靶细胞被NP特异性I类限制的CTL裂解。当MV经紫外线失活后,MHC I类分子对NP的呈递得以保留,但可被阻断病毒进入细胞的融合抑制剂所阻断。当MV用甲醛失活后,NP不再由MHC I类分子呈递,尽管它仍由MHC II类分子呈递给NP特异性II类限制的T细胞杂交瘤。这些数据表明,MV与CD46分子的结合是病毒与细胞融合的先决条件,且NP的胞质递送对于I类分子的呈递是必需的。此外,病毒的甲醛失活导致NP的I类限制呈递丧失,这是由于融合和NP的胞质递送被选择性废除所致。

相似文献

1
Formaldehyde inactivation of measles virus abolishes CD46-dependent presentation of nucleoprotein to murine class I-restricted CTLs but not to class II-restricted helper T cells.麻疹病毒经甲醛灭活后,可消除核蛋白依赖CD46向小鼠I类限制性细胞毒性T淋巴细胞的呈递,但对II类限制性辅助性T细胞的呈递无影响。
Virology. 1995 Sep 10;212(1):255-8. doi: 10.1006/viro.1995.1479.
2
Efficient MHC class II-restricted presentation of measles virus to T cells relies on its targeting to its cellular receptor human CD46 and involves an endosomal pathway.麻疹病毒向T细胞的高效MHC II类限制性呈递依赖于其靶向细胞受体人类CD46,并涉及内体途径。
Cell Biol Int. 1994 May;18(5):315-20. doi: 10.1006/cbir.1994.1080.
3
Serotype-specific and canine distemper virus cross-reactive H-2Kk-restricted cytotoxic T lymphocyte epitopes in the measles virus nucleoprotein.麻疹病毒核蛋白中血清型特异性及犬瘟热病毒交叉反应性的H-2Kk限制性细胞毒性T淋巴细胞表位
Virology. 1994 Aug 15;203(1):172-7. doi: 10.1006/viro.1994.1470.
4
Analysis of the contribution of CTL epitopes in the immunobiology of morbillivirus infection.麻疹病毒感染免疫生物学中细胞毒性T淋巴细胞表位的贡献分析。
Virology. 1996 May 1;219(1):133-9. doi: 10.1006/viro.1996.0230.
5
Efficient major histocompatibility complex class II-restricted presentation of measles virus relies on hemagglutinin-mediated targeting to its cellular receptor human CD46 expressed by murine B cells.麻疹病毒高效的主要组织相容性复合体II类限制性提呈依赖于血凝素介导的靶向作用,靶向作用于由鼠B细胞表达的其细胞受体人类CD46。
J Exp Med. 1994 Jan 1;179(1):353-8. doi: 10.1084/jem.179.1.353.
6
The predominance of CD8+ T cells after infection with measles virus suggests a role for CD8+ class I MHC-restricted cytotoxic T lymphocytes (CTL) in recovery from measles. Clonal analyses of human CD8+ class I MHC-restricted CTL.感染麻疹病毒后CD8 + T细胞占优势,提示CD8 + I类MHC限制性细胞毒性T淋巴细胞(CTL)在麻疹恢复过程中发挥作用。对人类CD8 + I类MHC限制性CTL进行克隆分析。
J Immunol. 1990 Mar 15;144(6):2394-9.
7
Identification and characterization of T helper epitopes in the nucleoprotein of influenza A virus.甲型流感病毒核蛋白中辅助性T细胞表位的鉴定与特性分析
J Immunol. 1989 Nov 1;143(9):3007-14.
8
Dendritic cells process exogenous viral proteins and virus-like particles for class I presentation to CD8+ cytotoxic T lymphocytes.树突状细胞处理外源性病毒蛋白和病毒样颗粒,以便将其呈递给I类分子,进而呈递给CD8+细胞毒性T淋巴细胞。
Eur J Immunol. 1996 Nov;26(11):2595-600. doi: 10.1002/eji.1830261109.
9
A dominant Th epitope in influenza nucleoprotein. Analysis of the fine specificity and functional repertoire of T cells recognizing a single determinant.流感核蛋白中的一个显性Th表位。识别单一决定簇的T细胞的精细特异性和功能谱分析。
J Immunol. 1990 Apr 1;144(7):2730-7.
10
CTL escape viral variants. I. Generation and molecular characterization.细胞毒性T淋巴细胞逃逸病毒变体。I. 产生及分子特征
Virology. 1995 Jun 20;210(1):29-40. doi: 10.1006/viro.1995.1314.

引用本文的文献

1
Biotechnological Applications of an Insect-Specific Alphavirus.一种昆虫特异性甲病毒的生物技术应用
DNA Cell Biol. 2017 Dec;36(12):1045-1049. doi: 10.1089/dna.2017.4019. Epub 2017 Nov 21.
2
A chikungunya fever vaccine utilizing an insect-specific virus platform.一种利用昆虫特异性病毒平台的基孔肯雅热疫苗。
Nat Med. 2017 Feb;23(2):192-199. doi: 10.1038/nm.4253. Epub 2016 Dec 19.
3
Emerging roles and new functions of CD46.CD46的新作用与新功能
Springer Semin Immunopathol. 2005 Nov;27(3):345-58. doi: 10.1007/s00281-005-0002-3. Epub 2005 Nov 11.
4
Requirements for measles virus induction of RANTES chemokine in human astrocytoma-derived U373 cells.麻疹病毒在人星形细胞瘤来源的U373细胞中诱导RANTES趋化因子的条件
J Virol. 1999 Apr;73(4):3117-24. doi: 10.1128/JVI.73.4.3117-3124.1999.
5
Processing of the DRB1*1103-restricted measles virus nucleoprotein determinant 185-199 in the endosomal compartment.DRB1*1103限制的麻疹病毒核蛋白决定簇185 - 199在内体区室中的加工过程。
Clin Exp Immunol. 1998 Nov;114(2):228-35. doi: 10.1046/j.1365-2249.1998.00716.x.