• 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

[使用疫苗株MVA对人和动物进行正痘病毒免疫接种的经验]

[Experiences with immunization against orthopox viruses of humans and animals using vaccine strain MVA].

作者信息

Mahnel H, Mayr A

机构信息

Lehrstuhl für Mikrobiologie und Seuchenlehre, Infektions- und Seuchenmedizin, Tierärztliche Fakultät der Universität München.

出版信息

Berl Munch Tierarztl Wochenschr. 1994 Aug;107(8):253-6.

PMID:7945180
Abstract

Immunizations against orthopox virus infections require a replicating, but safe vaccinia virus. The strain MVA is well suited concerning this matter. Human beings and animals can be vaccinated without any risk. The virus propagated in cell culture is non-virulent and lost its contagiosity. Multiplication in vaccinated men and animals is limited and excretion does not happen. As known for other attenuated virus strains, there must be a minimal effective virus concentration in the vaccine, which is 10(7.5) TCID50 per ml for MVA. To achieve a solid basic immunity which endures for a minimal of one year, two parenteral applications of MVA at intervals of at least 3 weeks are necessary.

摘要

针对正痘病毒感染的免疫接种需要一种具有复制能力但安全的痘苗病毒。MVA毒株在这方面非常合适。人类和动物接种该疫苗均无任何风险。在细胞培养中繁殖的这种病毒无毒力且失去了传染性。在接种疫苗的人和动物体内的繁殖受到限制,不会发生病毒排泄。正如其他减毒病毒株一样,疫苗中必须有最低有效病毒浓度,MVA的最低有效病毒浓度为每毫升10(7.5) 半数组织培养感染剂量(TCID50)。为了获得至少持续一年的稳固基础免疫力,需要至少间隔3周进行两次MVA的肠胃外接种。

相似文献

1
[Experiences with immunization against orthopox viruses of humans and animals using vaccine strain MVA].[使用疫苗株MVA对人和动物进行正痘病毒免疫接种的经验]
Berl Munch Tierarztl Wochenschr. 1994 Aug;107(8):253-6.
2
Protection induced in mice against a lethal orthopox virus by the Lister strain of vaccinia virus and modified vaccinia virus Ankara (MVA).用痘苗病毒李斯特株和安卡拉改良痘苗病毒(MVA)诱导小鼠产生针对致死性正痘病毒的保护作用。
Vaccine. 2006 May 8;24(19):4152-60. doi: 10.1016/j.vaccine.2006.02.012. Epub 2006 Feb 20.
3
[TC marker of the attenuated vaccinia vaccide strain "MVA" in human cell cultures and protective immunization against orthopox diseases in animals].[人细胞培养物中减毒痘苗疫苗株“MVA”的TC标志物及动物中针对正痘病毒疾病的保护性免疫]
Zentralbl Veterinarmed B. 1976 Jun;23(5-6):417-30.
4
Vaccination against pox diseases under immunosuppressive conditions.免疫抑制条件下针对痘病的疫苗接种。
Dev Biol Stand. 1978;41:225-34.
5
[The resistance of a maternally-derived immunity of baby mice against mousepox--experiments regarding a special possibility of immunization with orthopox viruses (author's transl)].[幼鼠母源免疫对鼠痘的抵抗力——关于正痘病毒特殊免疫可能性的实验(作者译)]
Zentralbl Bakteriol B. 1979;169(5-6):495-509.
6
[The effectiveness of immunization with vaccinia virus type "MVA" against an infection with cowpox virus type "OPV 85" in rabbits].[痘苗病毒“MVA”免疫对兔感染牛痘病毒“OPV 85”的有效性]
Zentralbl Veterinarmed B. 1993 Mar;40(2):131-40.
7
Highly attenuated smallpox vaccine protects rabbits and mice against pathogenic orthopoxvirus challenge.高度减毒的天花疫苗可保护兔和小鼠免受致病性正痘病毒的攻击。
Vaccine. 2006 Apr 24;24(17):3686-94. doi: 10.1016/j.vaccine.2005.03.029.
8
Enhanced immunogenicity and protective effect conferred by vaccination with combinations of modified vaccinia virus Ankara and licensed smallpox vaccine Dryvax in a mouse model.在小鼠模型中,用改良安卡拉痘苗病毒和已获许可的天花疫苗Dryvax联合接种所赋予的增强免疫原性和保护作用。
Virology. 2005 Sep 1;339(2):164-75. doi: 10.1016/j.virol.2005.06.002.
9
Reexamination of the efficacy of vaccination against mousepox.对小鼠痘疫苗接种效果的重新检验。
Lab Anim Sci. 1985 Oct;35(5):473-6.
10
Controlling orthopoxvirus infections--200 years after Jenner's revolutionary immunization.控制正痘病毒感染——詹纳革命性免疫接种200年后
Arch Immunol Ther Exp (Warsz). 1996;44(5-6):373-8.

引用本文的文献

1
Whole genome sequencing of recombinant viruses obtained from co-infection and superinfection of Vero cells with modified vaccinia virus ankara vectored influenza vaccine and a naturally occurring cowpox virus.从感染和重组牛痘病毒的vero 细胞中同时感染和超感染的改良安卡拉痘苗病毒载体流感疫苗和天然牛痘病毒获得的重组病毒的全基因组测序。
Front Immunol. 2024 Apr 3;15:1277447. doi: 10.3389/fimmu.2024.1277447. eCollection 2024.
2
The Brighton Collaboration standardized template for collection of key information for risk/benefit assessment of a Modified Vaccinia Ankara (MVA) vaccine platform.布莱顿合作组织的改良安卡拉病毒(MVA)疫苗平台风险/效益评估关键信息采集标准化模板。
Vaccine. 2021 May 21;39(22):3067-3080. doi: 10.1016/j.vaccine.2020.08.050. Epub 2020 Oct 17.
3
Modulation of Cell Surface Receptor Expression by Modified Vaccinia Virus Ankara in Leukocytes of Healthy and HIV-Infected Individuals.修饰安卡拉痘苗病毒对健康个体和 HIV 感染者白细胞表面受体表达的调节作用。
Front Immunol. 2020 Sep 8;11:2096. doi: 10.3389/fimmu.2020.02096. eCollection 2020.
4
[Vaccine of the future].[未来的疫苗]
Rev Francoph Lab. 2019 May;2019(512):52-63. doi: 10.1016/S1773-035X(19)30258-8. Epub 2019 Apr 24.
5
Field Trial Vaccination against Cowpox in Two Alpaca Herds.在两个羊驼群中进行牛痘疫苗现场试验。
Viruses. 2020 Feb 20;12(2):234. doi: 10.3390/v12020234.
6
Modified Vaccinia Virus Ankara: History, Value in Basic Research, and Current Perspectives for Vaccine Development.安卡拉改良牛痘病毒:历史、基础研究价值及疫苗开发的当前展望
Adv Virus Res. 2017;97:187-243. doi: 10.1016/bs.aivir.2016.07.001. Epub 2016 Aug 1.
7
The influence of delivery vectors on HIV vaccine efficacy.不同载体对 HIV 疫苗效力的影响。
Front Microbiol. 2014 Aug 22;5:439. doi: 10.3389/fmicb.2014.00439. eCollection 2014.
8
Environmental risk assessment of clinical trials involving modified vaccinia virus Ankara (MVA)-based vectors.基于改良安卡拉痘苗病毒(MVA)载体的临床试验的环境风险评估。
Curr Gene Ther. 2013 Dec;13(6):413-20. doi: 10.2174/156652321306140103221941.
9
Clinical Efficacy of TroVax in the Treatment of Progressive Castration-resistant Prostate Cancer.特罗瓦克斯治疗进展性去势抵抗性前列腺癌的临床疗效。
Clin Med Insights Oncol. 2012;6:67-73. doi: 10.4137/CMO.S7654. Epub 2012 Jan 5.
10
Deletion of the A35 gene from Modified Vaccinia Virus Ankara increases immunogenicity and isotype switching.从改良安卡拉痘苗病毒中删除 A35 基因可提高免疫原性和同种型转换。
Vaccine. 2011 Apr 12;29(17):3276-83. doi: 10.1016/j.vaccine.2011.02.023. Epub 2011 Feb 23.