Hayashi T, Hotta H, Itoh M, Homma M
Department of Microbiology, Kobe University School of Medicine, Hyogo, Japan.
J Gen Virol. 1991 Apr;72 ( Pt 4):979-82. doi: 10.1099/0022-1317-72-4-979.
Proteolytic activation of Sendai virus in the lungs of mice is necessary to cause pneumopathogenicity. Using Sendai virus-infected lung block cultures, protease inhibitors were tested for their antiviral effect by examining inhibition of proteolytic activation. Among the inhibitors tested, a serine protease, aprotinin, was shown to be most effective. In vivo protection experiments demonstrated that aprotinin, when administered intranasally, could confer protection on mice against lethal Sendai virus pneumonia through the same mechanism as observed in the in vitro system. The present study provides an experimental basis for the use of protease inhibitors as antiviral drugs.
仙台病毒在小鼠肺部的蛋白水解激活对于引发肺致病性是必要的。利用感染仙台病毒的肺组织块培养物,通过检测对蛋白水解激活的抑制作用来测试蛋白酶抑制剂的抗病毒效果。在所测试的抑制剂中,丝氨酸蛋白酶抑肽酶显示出最有效。体内保护实验表明,经鼻给药时,抑肽酶可通过与体外系统中观察到的相同机制,为小鼠提供针对致死性仙台病毒肺炎的保护作用。本研究为使用蛋白酶抑制剂作为抗病毒药物提供了实验依据。