Crance J M, Deloince R, Leveque F, Jouan A, Trépo C
Unité de Biologie Moléculaire, Centre de Recherches du Service de Santé des Armées, La Tronche, France.
C R Acad Sci III. 1994 Jan;317(1):94-7.
Two recombinant interferons-alpha (IFNs-alpha) were assayed for their antiviral effect on hepatitis A virus (HAV) replication in the human hepatoma cell line PLC/PRF/5. IFN alpha-2a and IFN alpha-2b resulted in concentration-dependent inhibition of HAV antigen expression and HAV infectivity at non toxic concentrations. Their selectivity indices, calculated as the ratio of the dose that reduced the number of viable cells to 50% (CD50) to the effective dose that inhibited 50% of viral antigen expression (ED50) were > 1000. Recombinant IFN-alpha emerged, from the present study, as a promising candidate for chemotherapy of hepatitis A.
检测了两种重组α干扰素(IFNs-α)对甲型肝炎病毒(HAV)在人肝癌细胞系PLC/PRF/5中复制的抗病毒作用。IFNα-2a和IFNα-2b在无毒浓度下导致HAV抗原表达和HAV感染性呈浓度依赖性抑制。它们的选择性指数(计算为使活细胞数量减少50%的剂量(CD50)与抑制50%病毒抗原表达的有效剂量(ED50)之比)>1000。从本研究来看,重组α干扰素成为甲型肝炎化疗的一个有前景的候选药物。