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Confronting the next influenza pandemic with anti-inflammatory and immunomodulatory agents: why they are needed and how they might work

机译:用抗炎和免疫调节剂应对下一次流感大流行:为什么需要它们以及它们如何起作用

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Despite the best efforts of influenza scientists, companies and health officials to prepare for the next pandemic, most of the world's people will not have access to affordable supplies of vaccines and antiviral agents. They will have to rely on 19th century public health 'technologies' to see them through. In the 21st century, science ought to be able to provide something better. Influenza scientists study the molecular characteristics of influenza viruses and their signaling effects in cell culture and animal models of infection. While these studies have been enormously informative, they have been unable to explain the system-wide effects of influenza on the host, the increased mortality of younger adults in the 1918 influenza pandemic and the much lower mortality rates in children who were more commonly infected with the 1918 virus. Experiments by non-influenza scientists have defined common cell signaling pathways for acute lung injury caused by different agents, including inactivated H5N1 influenza virus. These pathways include several molecular targets that are up-regulated in acute lung injury and down-regulated by anti-inflammatory and immunomodulatory agents, including statins, fibrates, and glitazones. These agents also help reverse the mitochondrial dysfunction that accompanies multi-organ failure, something often seen in fatal Influenza. Observational studies suggest that statins are beneficial in treating patients with pneumonia (there are no such studies for fibrates and glitazones). Other studies suggest that these agents might be able to 'roll back' the self-damaging host response of young adults to the less damaging response of children and thus save lives. Research is urgently needed to determine whether these and other agents that modify the host response might be useful in managing H5N1 influenza and the next pandemic.
机译:尽管流感科学家,公司和卫生官员尽了最大的努力为下一次大流行做准备,但世界上大多数人将无法获得负担得起的疫苗和抗病毒剂。他们将不得不依靠19世纪的公共卫生“技术”来了解它们。在21世纪,科学应该能够提供更好的东西。流感科学家研究了流感病毒的分子特征及其在细胞培养和感染动物模型中的信号传导作用。尽管这些研究提供了极大的信息,但它们无法解释流感对宿主的全系统影响,1918年流感大流行中年轻成年人的死亡率增加以及更常见的感染儿童的死亡率低得多1918年的病毒。非流感科学家的实验已经定义了由不同因素(包括灭活的H5N1流感病毒)引起的急性肺损伤的常见细胞信号通路。这些途径包括在急性肺损伤中上调而在抗炎药和免疫调节剂(包括他汀类,贝特类和格列酮类)中下调的几种分子靶标。这些药物还有助于逆转伴随多器官衰竭的线粒体功能障碍,这在致命的流感中经常可见。观察性研究表明,他汀类药物在治疗肺炎患者方面是有益的(没有关于贝特类和格列酮类的研究)。其他研究表明,这些因素可能能够使年轻人的自我伤害性宿主反应“退缩”到对儿童危害较小的反应中,从而挽救生命。迫切需要进行研究以确定这些和改变宿主反应的其他药物在管理H5N1流感和下一次大流行中是否有用。

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