禽流感。

Tsung-Zu Wu, Li-Min Huang
{"title":"禽流感。","authors":"Tsung-Zu Wu, Li-Min Huang","doi":"10.32388/y54t02","DOIUrl":null,"url":null,"abstract":"Influenza is an old disease but remains vital nowadays. Three types of influenza viruses, namely A, B, C, have been identified; among them influenza A virus has pandemic potential. The first outbreak of human illness due to avian influenza virus (H5N1) occurred in 1997 in Hong Kong with a mortality of 30%. The most recent outbreak of the avian influenza epidemic has been going on in Asian countries since 2003. As of March 2005, 44 incidental human infections and 32 deaths have been documented. Human influenza viruses differ with other avian influenza viruses on the choice of cellular receptors. Avian influenza viruses bind to cell-surface glycoproteins or glycolipids containing terminal sialyl-galactosyl residues linked by 2-3-linkage [Neu5Ac(alpha2-3)Gal], whereas human viruses, including the earliest available isolates from the 1957 and 1968 pandemics, bind to receptors that contain terminal 2-6-linked sialyl-galactosyl moieties [Neu5Ac(alpha2-6)Gal]. Recent evidence suggests that human bronchial ciliated epithelial cells contain Neu5Ac(alpha2-3)Gal and can be infected with avian influenza viruses. Nevertheless, avian influenza viruses can not infect non-ciliated bronchial epithelial cells. Hence, adaptation of the avian influenza virus to nonciliated cells is a prerequisite for a pandemic virus to emerge. Biological behaviors of influenza viruses indicate that once a pandemic virus emerges, isolation is not likely to contain this epidemic. A specific vaccine against the pandemic strain will not be available until 6 to 12 months after the inception of the pandemic. Judicious use of antiviral agents and stringent disease control measures are imperative to decrease the impact of a future pandemic.","PeriodicalId":10018,"journal":{"name":"Chang Gung medical journal","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2020-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Avian influenza.\",\"authors\":\"Tsung-Zu Wu, Li-Min Huang\",\"doi\":\"10.32388/y54t02\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Influenza is an old disease but remains vital nowadays. Three types of influenza viruses, namely A, B, C, have been identified; among them influenza A virus has pandemic potential. The first outbreak of human illness due to avian influenza virus (H5N1) occurred in 1997 in Hong Kong with a mortality of 30%. The most recent outbreak of the avian influenza epidemic has been going on in Asian countries since 2003. As of March 2005, 44 incidental human infections and 32 deaths have been documented. Human influenza viruses differ with other avian influenza viruses on the choice of cellular receptors. Avian influenza viruses bind to cell-surface glycoproteins or glycolipids containing terminal sialyl-galactosyl residues linked by 2-3-linkage [Neu5Ac(alpha2-3)Gal], whereas human viruses, including the earliest available isolates from the 1957 and 1968 pandemics, bind to receptors that contain terminal 2-6-linked sialyl-galactosyl moieties [Neu5Ac(alpha2-6)Gal]. Recent evidence suggests that human bronchial ciliated epithelial cells contain Neu5Ac(alpha2-3)Gal and can be infected with avian influenza viruses. Nevertheless, avian influenza viruses can not infect non-ciliated bronchial epithelial cells. Hence, adaptation of the avian influenza virus to nonciliated cells is a prerequisite for a pandemic virus to emerge. Biological behaviors of influenza viruses indicate that once a pandemic virus emerges, isolation is not likely to contain this epidemic. A specific vaccine against the pandemic strain will not be available until 6 to 12 months after the inception of the pandemic. Judicious use of antiviral agents and stringent disease control measures are imperative to decrease the impact of a future pandemic.\",\"PeriodicalId\":10018,\"journal\":{\"name\":\"Chang Gung medical journal\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-02-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chang Gung medical journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32388/y54t02\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chang Gung medical journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32388/y54t02","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

流行性感冒是一种古老的疾病,但现在仍然很严重。已经确定了三种流感病毒,即A、B、C型;其中甲型流感病毒具有大流行的潜力。香港于1997年首次爆发由禽流感病毒(H5N1)引起的人类疾病,死亡率为30%。最近一次禽流感疫情自2003年以来一直在亚洲国家爆发。截至2005年3月,已记录有44人意外感染和32人死亡。人流感病毒与其他禽流感病毒在细胞受体的选择上不同。禽流感病毒与细胞表面糖蛋白或糖脂结合,这些糖蛋白或糖脂含有由2-3连锁连接的末端唾液-半乳糖基残基[Neu5Ac(alpha2-3)Gal],而人类病毒,包括1957年和1968年大流行中最早可获得的分离株,与含有末端2-6连锁的唾液-半乳糖基片段[Neu5Ac(alpha2-6)Gal]的受体结合。最近的证据表明,人支气管纤毛上皮细胞含有Neu5Ac(alpha2-3)Gal,可感染禽流感病毒。然而,禽流感病毒不能感染非纤毛支气管上皮细胞。因此,禽流感病毒对非纤毛细胞的适应是大流行病毒出现的先决条件。流感病毒的生物学行为表明,一旦出现大流行病毒,隔离不太可能遏制这种流行病。针对大流行毒株的特异性疫苗要到大流行开始后6至12个月才能获得。明智地使用抗病毒药物和严格的疾病控制措施是减少未来大流行影响的必要条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Avian influenza.
Influenza is an old disease but remains vital nowadays. Three types of influenza viruses, namely A, B, C, have been identified; among them influenza A virus has pandemic potential. The first outbreak of human illness due to avian influenza virus (H5N1) occurred in 1997 in Hong Kong with a mortality of 30%. The most recent outbreak of the avian influenza epidemic has been going on in Asian countries since 2003. As of March 2005, 44 incidental human infections and 32 deaths have been documented. Human influenza viruses differ with other avian influenza viruses on the choice of cellular receptors. Avian influenza viruses bind to cell-surface glycoproteins or glycolipids containing terminal sialyl-galactosyl residues linked by 2-3-linkage [Neu5Ac(alpha2-3)Gal], whereas human viruses, including the earliest available isolates from the 1957 and 1968 pandemics, bind to receptors that contain terminal 2-6-linked sialyl-galactosyl moieties [Neu5Ac(alpha2-6)Gal]. Recent evidence suggests that human bronchial ciliated epithelial cells contain Neu5Ac(alpha2-3)Gal and can be infected with avian influenza viruses. Nevertheless, avian influenza viruses can not infect non-ciliated bronchial epithelial cells. Hence, adaptation of the avian influenza virus to nonciliated cells is a prerequisite for a pandemic virus to emerge. Biological behaviors of influenza viruses indicate that once a pandemic virus emerges, isolation is not likely to contain this epidemic. A specific vaccine against the pandemic strain will not be available until 6 to 12 months after the inception of the pandemic. Judicious use of antiviral agents and stringent disease control measures are imperative to decrease the impact of a future pandemic.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信