• 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

麻疹卷土重来与药物研发。

Measles Resurgence and Drug Development.

机构信息

Institute for Biomedical Sciences, Georgia State University, Atlanta, GA 30303, USA.

出版信息

Curr Opin Virol. 2020 Apr;41:8-17. doi: 10.1016/j.coviro.2020.02.007. Epub 2020 Apr 1.

DOI:10.1016/j.coviro.2020.02.007
PMID:32247280
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7492439/
Abstract

Measles caused an estimated minimum of one million fatalities annually before vaccination. Outstanding progress towards controlling the virus has been made since the measles vaccine was introduced, but reduction of measles case-fatalities has stalled at around 100,000 annually for the last decade and a 2019 resurgence in several geographical regions threatens some of these past accomplishments. Whereas measles eradication through vaccination is feasible, a potentially open-ended endgame of elimination may loom. Other than doubling-down on existing approaches, is it worthwhile to augment vaccination efforts with antiviral therapeutics to solve the conundrum? This question is hypothetical at present, since no drugs have yet been approved specifically for the treatment of measles, or infection by any other pathogen of the paramyxovirus family. This article will consider obstacles that have hampered anti-measles and anti-paramyxovirus drug development, discuss MeV-specific challenges of clinical testing, and define drug properties suitable to address some of these problems.

摘要

在疫苗接种之前,麻疹每年估计导致至少 100 万人死亡。自麻疹疫苗问世以来,在控制该病毒方面取得了杰出进展,但在过去十年中,麻疹病例死亡率每年减少约 10 万,2019 年几个地理区域的疫情反弹威胁到了其中一些过去的成就。虽然通过疫苗接种根除麻疹是可行的,但可能会出现一个无限期的消灭终点。除了加倍现有方法之外,是否值得通过抗病毒疗法来加强疫苗接种工作,以解决这一难题?目前,这个问题还只是假设,因为还没有专门批准用于治疗麻疹或副粘病毒科任何其他病原体感染的药物。本文将考虑阻碍抗麻疹和抗副粘病毒药物开发的障碍,讨论 MeV 临床检测的具体挑战,并定义适合解决其中一些问题的药物特性。

相似文献

1
Measles Resurgence and Drug Development.麻疹卷土重来与药物研发。
Curr Opin Virol. 2020 Apr;41:8-17. doi: 10.1016/j.coviro.2020.02.007. Epub 2020 Apr 1.
2
Measles control--can measles virus inhibitors make a difference?麻疹控制——麻疹病毒抑制剂能发挥作用吗?
Curr Opin Investig Drugs. 2009 Aug;10(8):811-20.
3
Will Measles Virus or Humanity Win the International "Fitness" Challenge?麻疹病毒还是人类会赢得这场国际“适应性”挑战?
Annu Rev Virol. 2019 Sep 29;6(1):iii-vii. doi: 10.1146/annurev-vi-06-072619-100011.
4
Progress towards measles elimination -South-East Asia Region, 2003-2013.2003 - 2013年东南亚区域在消除麻疹方面取得的进展
Wkly Epidemiol Rec. 2015 Jun 12;90(24):297-305.
5
Measles outbreak after 12 years without endemic transmission, Portugal, February to May 2017.2017年2月至5月,葡萄牙在12年无本土传播后出现麻疹疫情。
Euro Surveill. 2017 Jun 8;22(23). doi: 10.2807/1560-7917.ES.2017.22.23.30548.
6
Measles virus.麻疹病毒
Hum Vaccin Immunother. 2015;11(1):21-6. doi: 10.4161/hv.34298. Epub 2014 Nov 1.
7
Measles, the need for a paradigm shift.麻疹,需要范式转变。
Eur J Epidemiol. 2019 Oct;34(10):897-915. doi: 10.1007/s10654-019-00569-4. Epub 2019 Oct 17.
8
The Americas: paving the road toward global measles eradication.美洲:为全球麻疹消除铺平道路。
J Infect Dis. 2011 Jul;204 Suppl 1:S270-8. doi: 10.1093/infdis/jir166.
9
Progress towards measles elimination, Philippines, 1998–2014.1998 - 2014年菲律宾在消除麻疹方面取得的进展。
Wkly Epidemiol Rec. 2015 Apr;90(15):149-59.
10
Measles.麻疹。
Lancet. 2017 Dec 2;390(10111):2490-2502. doi: 10.1016/S0140-6736(17)31463-0. Epub 2017 Jun 30.

引用本文的文献

1
[Programmed cell death in paramyxovirus infection].[副粘病毒感染中的程序性细胞死亡]
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2025 May 25;54(3):399-410. doi: 10.3724/zdxbyxb-2024-0512.
2
Structural basis of paramyxo- and pneumovirus polymerase inhibition by non-nucleoside small-molecule antivirals.副黏病毒和肺病毒聚合酶非核苷小分子抗病毒药物抑制的结构基础。
Antimicrob Agents Chemother. 2024 Oct 8;68(10):e0080024. doi: 10.1128/aac.00800-24. Epub 2024 Aug 20.
3
Design and Execution of In Vitro Polymerase Assays for Measles Virus and Related Mononegaviruses.用于麻疹病毒和相关副黏液病毒的体外聚合酶检测的设计与执行。
Methods Mol Biol. 2024;2808:19-33. doi: 10.1007/978-1-0716-3870-5_3.
4
Helical peptides with disordered regions for measles viruses provide new generalized insights into fusion inhibitors.具有针对麻疹病毒无序区域的螺旋肽为融合抑制剂提供了新的普遍见解。
iScience. 2024 Jan 17;27(2):108961. doi: 10.1016/j.isci.2024.108961. eCollection 2024 Feb 16.
5
Therapeutic mitigation of measles-like immune amnesia and exacerbated disease after prior respiratory virus infections in ferrets.雪貂中先前呼吸道病毒感染后麻疹样免疫遗忘和加重疾病的治疗缓解。
Nat Commun. 2024 Feb 8;15(1):1189. doi: 10.1038/s41467-024-45418-5.
6
Paramyxoviruses: Pathogenesis, Vaccines, Antivirals, and Prototypes for Pandemic Preparedness.副黏液病毒:发病机制、疫苗、抗病毒药物以及大流行防范的原型。
J Infect Dis. 2023 Oct 18;228(Suppl 6):S390-S397. doi: 10.1093/infdis/jiad123.
7
Effect of remdesivir post-exposure prophylaxis and treatment on pathogenesis of measles in rhesus macaques.瑞德西韦暴露后预防和治疗对恒河猴麻疹发病机制的影响。
Sci Rep. 2023 Apr 20;13(1):6463. doi: 10.1038/s41598-023-33572-7.
8
C Proteins: Controllers of Orderly Paramyxovirus Replication and of the Innate Immune Response.C 蛋白:调节副黏病毒复制和固有免疫反应的控制器。
Viruses. 2022 Jan 12;14(1):137. doi: 10.3390/v14010137.
9
Highly Potent Host-Specific Small-Molecule Inhibitor of Paramyxovirus and Pneumovirus Replication with High Resistance Barrier.高效能、宿主特异性的小分子量病毒抑制剂,对副黏病毒和肺炎病毒具有高效抵抗屏障的复制能力。
mBio. 2021 Dec 21;12(6):e0262121. doi: 10.1128/mBio.02621-21. Epub 2021 Nov 2.
10
An update on the progress of galidesivir (BCX4430), a broad-spectrum antiviral.加拉西韦(BCX4430)作为一种广谱抗病毒药物的研究进展更新。
Antiviral Res. 2021 Nov;195:105180. doi: 10.1016/j.antiviral.2021.105180. Epub 2021 Sep 20.

本文引用的文献

1
A Phase 2, Randomized, Double-blind, Placebo-Controlled Trial of Presatovir for the Treatment of Respiratory Syncytial Virus Upper Respiratory Tract Infection in Hematopoietic-Cell Transplant Recipients.一项评估 Presatovir 治疗造血干细胞移植受者呼吸道合胞病毒上呼吸道感染的 2 期、随机、双盲、安慰剂对照研究。
Clin Infect Dis. 2020 Dec 31;71(11):2777-2786. doi: 10.1093/cid/ciz1166.
2
Measles virus infection diminishes preexisting antibodies that offer protection from other pathogens.麻疹病毒感染会削弱提供针对其他病原体保护的预先存在的抗体。
Science. 2019 Nov 1;366(6465):599-606. doi: 10.1126/science.aay6485.
3
Incomplete genetic reconstitution of B cell pools contributes to prolonged immunosuppression after measles.麻疹后 B 细胞池不完全遗传重建导致免疫抑制延长。
Sci Immunol. 2019 Nov 1;4(41). doi: 10.1126/sciimmunol.aay6125.
4
Small molecule grp94 inhibitors block dengue and Zika virus replication.小分子 Grp94 抑制剂可阻断登革热和 Zika 病毒复制。
Antiviral Res. 2019 Nov;171:104590. doi: 10.1016/j.antiviral.2019.104590. Epub 2019 Aug 14.
5
Response to Comment on "Long-term measles-induced immunomodulation increases overall childhood infectious disease mortality".对“麻疹长期诱导的免疫调节增加儿童期整体传染病死亡率”一文的评论的回复。
Science. 2019 Jul 12;365(6449). doi: 10.1126/science.aax6498.
6
Identification and Efficacy Assessment of Approved Orally Bioavailable Human Host Protein-Targeting Drugs With Broad Anti-influenza A Activity.鉴定和评估具有广谱抗甲型流感活性的已批准口服生物利用度的人源宿主蛋白靶向药物。
Front Immunol. 2019 Jun 5;10:1097. doi: 10.3389/fimmu.2019.01097. eCollection 2019.
7
Measles Virus Bearing Measles Inclusion Body Encephalitis-Derived Fusion Protein Is Pathogenic after Infection via the Respiratory Route.麻疹病毒携带麻疹包涵体脑炎衍生融合蛋白经呼吸道感染后具有致病性。
J Virol. 2019 Apr 3;93(8). doi: 10.1128/JVI.01862-18. Print 2019 Apr 15.
8
Progress Toward Regional Measles Elimination - Worldwide, 2000-2017.迈向区域消除麻疹目标的进展 - 全球,2000-2017 年。
MMWR Morb Mortal Wkly Rep. 2018 Nov 30;67(47):1323-1329. doi: 10.15585/mmwr.mm6747a6.
9
Post-exposure prophylaxis for measles with immunoglobulins revised recommendations of the standing committee on vaccination in Germany.接触后用免疫球蛋白预防麻疹——德国疫苗接种常设委员会的修订建议。
Vaccine. 2018 Dec 18;36(52):7916-7922. doi: 10.1016/j.vaccine.2018.10.070. Epub 2018 Nov 23.
10
Impact and longevity of measles-associated immune suppression: a matched cohort study using data from the THIN general practice database in the UK.麻疹相关免疫抑制的影响和持久性:一项基于英国 THIN 全科医生数据库的匹配队列研究。
BMJ Open. 2018 Nov 8;8(11):e021465. doi: 10.1136/bmjopen-2017-021465.