Pfeffer L M, Dinarello C A, Herberman R B, Williams B R, Borden E C, Bordens R, Walter M R, Nagabhushan T L, Trotta P P, Pestka S
Department of Pathology, University of Tennessee Health Science Center, Memphis 38163, USA.
Cancer Res. 1998 Jun 15;58(12):2489-99.
IFNs were first described as potent antiviral agents 40 years ago, and recombinant IFN-alpha2a and IFN-alpha2b were approved for the treatment of hairy cell leukemia just 11 years ago. Today, alpha-IFNs are approved worldwide for the treatment of a variety of malignancies and virologic diseases. Although the exact mechanism of action of IFN-alpha in the treatment of such diseases is not fully understood, many advances have been made in the characterization of the physicochemical and diverse biological properties of this highly pleiotropic cytokine. Here we review recent developments in our understanding of the antiviral and immunoregulatory properties of IFN-alpha, the nature of the multisubunit IFN-alpha receptor, and the molecular mechanisms of signal transduction. Where available, we have included comparative data on recombinant alpha-IFNs derived from both naturally occurring and nonnaturally occurring synthetic genes. We also review clinical data and data on the side effects and antigenicity of different sources of recombinant alpha-IFNs in humans. These latter topics are of clinical interest, because they may potentially affect the efficacy of these various products. Hopefully, what is already known about IFN will prompt further exploration into the mechanism(s) of action of IFN-alpha and thus deliver new applications for this prototypic cytokine, whose full therapeutic potential is yet to be realized.
40年前,干扰素首次被描述为强效抗病毒剂,而重组干扰素α2a和干扰素α2b在仅仅11年前才被批准用于治疗毛细胞白血病。如今,α干扰素在全球范围内被批准用于治疗多种恶性肿瘤和病毒疾病。尽管干扰素α治疗此类疾病的确切作用机制尚未完全明了,但在表征这种具有高度多效性的细胞因子的物理化学及多种生物学特性方面已取得了许多进展。在此,我们综述了近期在理解干扰素α的抗病毒和免疫调节特性、多亚基干扰素α受体的性质以及信号转导分子机制方面的进展。在可行的情况下,我们纳入了来自天然和非天然合成基因的重组α干扰素的比较数据。我们还综述了临床数据以及不同来源的重组α干扰素在人体中的副作用和抗原性数据。后述这些主题具有临床意义,因为它们可能会潜在影响这些不同产品的疗效。希望已有的关于干扰素的知识能促使人们进一步探索干扰素α的作用机制,从而为这种原型细胞因子带来新的应用,其全部治疗潜力尚未得到充分发挥。