Fediakina I T, Shchelkanov M Iu, Deriabin P G, Leneva I A, Gudova N V, Kondrat'eva T V, L'vov D K
Antibiot Khimioter. 2011;56(3-4):3-9.
The data on cytotoxicity and antiviral activity of commercial antivirals, such as Remantadine, Oseltamivir, Arbidol and Ribavirin in the MDCK cell culture infected with highly pathogenic (H5N1) and pandemic 2009 (H1N1) influenza A viruses are presented. The study of the antiviral activity of antivirals in the MDCK cells culture demonstrated that Arbidol, Rimantadine and Ribavirin efficiently inhibited reproduction of the highly pathogenic H5N1 influenza viruses isolated from sick birds. Arbidol and Oseltamivir carboxylate selectively inhibited reproduction of the pandemic 2009 H1N1 influenza A viruses with changed specificity to the cell receptors, causing severe influenza in men, while remantadine had no effect on their reproduction.
本文展示了在感染高致病性(H5N1)和2009年大流行(H1N1)甲型流感病毒的MDCK细胞培养物中,金刚乙胺、奥司他韦、阿比朵尔和利巴韦林等商用抗病毒药物的细胞毒性和抗病毒活性数据。在MDCK细胞培养物中对抗病毒药物的抗病毒活性研究表明,阿比朵尔、金刚乙胺和利巴韦林可有效抑制从病禽中分离出的高致病性H5N1流感病毒的繁殖。阿比朵尔和奥司他韦羧酸盐选择性地抑制了对细胞受体特异性发生改变的2009年大流行H1N1甲型流感病毒的繁殖,这种病毒会在人类中引发严重流感,而金刚乙胺对其繁殖没有影响。