Johnson H M, Baron S
CRC Crit Rev Biochem. 1976 Nov;4(2):203-27. doi: 10.3109/10409237609105459.
The discovery of interferon in 1957 by Drs. Isaacs and Lindenmann led to major revisions in the concepts of man's defenses against viral infections. There are at least two types of interferon. Along with their antiviral properties, they have recently been shown to exert a suppressive effect on the humoral and cellular immune response; they affect both B and T lymphocytes. A variety of substances, including virus, polyribonucleotides, and mitogens for T lymphocytes, are good interferon inducers. T lymphocytes seem to be necessary for these inducers to exert their immunosuppressive effects. The immunosuppressive effects of interferon inducers suggests that interferons may be mediators of suppressor T lymphocyte effects. In the virus system, interferon does not exert its antiviral effects by direct action on the virus, but rather derepresses a cell gene that results in the production of an antiviral protein. This antiviral protein is probably the mediator of inhibition of virus replication. This is a complex sequence of events that results in the interaction of interferon with the cell membrane and the resulting production of the antiviral state in the cell. This review will examine the various steps of this involved process.
1957年,艾萨克斯博士和林登曼博士发现了干扰素,这使得人们对人体抵御病毒感染的概念有了重大修正。干扰素至少有两种类型。除了具有抗病毒特性外,它们最近还被证明对体液免疫和细胞免疫反应有抑制作用;它们对B淋巴细胞和T淋巴细胞都有影响。多种物质,包括病毒、多聚核糖核苷酸和T淋巴细胞的促有丝分裂原,都是良好的干扰素诱导剂。T淋巴细胞似乎是这些诱导剂发挥免疫抑制作用所必需的。干扰素诱导剂的免疫抑制作用表明,干扰素可能是抑制性T淋巴细胞作用的介质。在病毒系统中,干扰素并非通过直接作用于病毒来发挥其抗病毒作用,而是解除对一个细胞基因的抑制,该基因导致产生一种抗病毒蛋白。这种抗病毒蛋白可能是抑制病毒复制的介质。这是一系列复杂的事件,导致干扰素与细胞膜相互作用,并在细胞中产生抗病毒状态。这篇综述将探讨这一复杂过程的各个步骤。