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急性呼吸道感染的抗病毒化疗方法。

Approaches to antiviral chemotherapy for acute respiratory infections.

作者信息

Shigeta S

机构信息

Department of Microbiology, Fukushima Medical College, Japan.

出版信息

Antivir Chem Chemother. 1998 Mar;9(2):93-107. doi: 10.1177/095632029800900201.

Abstract

The causative agents of acute respiratory infections (ARI) in infants and children are mostly thought to be viruses. Some ARI in adult patients may be caused by bacteria but most often the causes are virus infections. When ARI affect immunocompromised patients or the elderly the mortality rates are significantly higher than in immunocompetent individuals. Many types of viruses cause ARI. Among them, influenza viruses A and B and respiratory syncytial virus (RSV) are thought to be the most important because of the severity of illness after infection and their high communicability in the human population. Recently, several novel antiviral drugs against ARI have been developed and some are proceeding in clinical trials. This review covers current investigations into antiviral compounds targeted at several points in the virus life-cycle. This includes PM-523, which broadly inhibits ortho- and paramyxo-viruses, two neuraminidase inhibitors for influenza virus, neutralizing antibody to RSV and chimeric soluble ICAM-1-IgA molecules targeted against rhinoviruses.

摘要

婴幼儿急性呼吸道感染(ARI)的致病原大多被认为是病毒。成年患者的一些ARI可能由细菌引起,但大多数情况下病因是病毒感染。当ARI影响免疫功能低下的患者或老年人时,死亡率显著高于免疫功能正常的个体。许多类型的病毒会引发ARI。其中,甲型和乙型流感病毒以及呼吸道合胞病毒(RSV)被认为是最重要的,因为感染后病情严重且在人群中传播性高。最近,已经研发出几种针对ARI的新型抗病毒药物,有些正在进行临床试验。本综述涵盖了针对病毒生命周期中几个环节的抗病毒化合物的当前研究。这包括能广泛抑制正粘病毒和副粘病毒的PM - 523、两种用于流感病毒的神经氨酸酶抑制剂、针对RSV的中和抗体以及针对鼻病毒的嵌合可溶性细胞间粘附分子1 - IgA分子。

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