病毒学
病毒
大流行
干扰素
甲型流感病毒
生物
人流感
微生物学
医学
2019年冠状病毒病(COVID-19)
传染病(医学专业)
疾病
病理
作者
Chun’e Xu,Xiaohong Song,Ling Fu,Dayong Dong,Shipo Wu,Guanlin Li,Shaoqiong Yi,Ting Yu,Rui Yu,Lihua Hou,Wei Chen
出处
期刊:Viral Immunology
[Mary Ann Liebert]
日期:2011-10-01
卷期号:24 (5): 369-374
被引量:11
标识
DOI:10.1089/vim.2011.0003
摘要
The pandemic 2009 H1N1 influenza virus broke out in North America and spread rapidly throughout the world. The type I interferon (IFN) response represents one of the first lines of defense against influenza virus infections. In this study, the protective potential of human exogenous IFN-ω against pandemic 2009 A (H1N1) influenza virus was assessed both in vitro and in guinea pigs. The viral loads of pandemic 2009 A (H1N1) influenza virus strains A/California/04/2009 and A/Beijing/501/2009 were reduced by up to 5000-fold in Caco-2 cells by the addition of human IFN-ω. With daily intranasal treatment with human IFN-ω the viral load of pandemic 2009 A (H1N1) influenza virus strain A/California/04/2009 decreased by 1000-fold in lung tissues of guinea pigs. These results provide strong support for the application of human IFN-ω pretreatment to human influenza control.
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