Rubin B Y, Gupta S L
Proc Natl Acad Sci U S A. 1980 Oct;77(10):5928-32. doi: 10.1073/pnas.77.10.5928.
Treatment of human fibroblast FS-4 cultures with human type II interferon preparations induced the synthesis of at least four proteins that were similar in size to four of the five proteins induced by type I interferons (Mr 120,000, 88,000, 67,000, and 56,000). However, the Mr 67,000 and 56,000 proteins were induced more strongly by type II than by type I interferon, and a counterpart of a Mr 80,000 protein induced by type I interferons was not noticeably induced by type II interferon preparations. We therefore compared type I and type II interferons for relative antiviral activities against different viruses (vesicular stomatitis, encephalomyocarditis, and vaccinia viruses and reovirus) and for cell growth-inhibitory activities on various cell types. The replication of vesicular stomatitis and encephalomyocarditis viruses was inhibited more strongly by type I interferon, whereas reovirus and vaccinia virus showed greater sensitivity to type II interferon preparations. This indicates that viruses may differ in their sensitivity to human type I and type II interferons and that the antiviral mechanisms induced by type I and type II interferons may have significant differences. The type I and type II interferons may have significant differences. The type I and type II interferons may also differ in their efficacies as antiproliferative agents. Type II interferon preparations at 2.5 units/ml inhibited the incorporatin of [3H]thymidine to a greater extent than did type I interferon at 400 units/ml. (For both type I and type II interferons, the unit of interferon activity was defined as the concentration that decreased the yield of vesicular stomatitis virus by 50% in FS-4 cultures.) Furthermore, whereas type II interferon preparations had a reversible cytostatic effect on normal human fibroblasts at 10 units/ml, the transformed cells tested (HeLa, osteosarcoma, U-amnion) showed extensive cell death, thus indicating that it may have a cytocidal effect on certain tumor cells. It appears that human type II interferon (or a factor present in these preparations) may be a potent antitumor agent.
用人Ⅱ型干扰素制剂处理人成纤维细胞FS - 4培养物,诱导产生了至少四种蛋白质,其大小与Ⅰ型干扰素诱导产生的五种蛋白质中的四种相似(分子量分别为120,000、88,000、67,000和56,000)。然而,Ⅱ型干扰素诱导产生的分子量为67,000和56,000的蛋白质比Ⅰ型干扰素诱导产生的更强,并且Ⅰ型干扰素诱导产生的分子量为80,000的蛋白质的对应物在Ⅱ型干扰素制剂处理下未明显诱导产生。因此,我们比较了Ⅰ型和Ⅱ型干扰素对不同病毒(水疱性口炎病毒、脑心肌炎病毒、痘苗病毒和呼肠孤病毒)的相对抗病毒活性以及对各种细胞类型的细胞生长抑制活性。水疱性口炎病毒和脑心肌炎病毒的复制受Ⅰ型干扰素抑制更强,而呼肠孤病毒和痘苗病毒对Ⅱ型干扰素制剂表现出更高的敏感性。这表明病毒对人Ⅰ型和Ⅱ型干扰素的敏感性可能不同,并且Ⅰ型和Ⅱ型干扰素诱导的抗病毒机制可能存在显著差异。Ⅰ型和Ⅱ型干扰素可能存在显著差异。Ⅰ型和Ⅱ型干扰素作为抗增殖剂的效力也可能不同。2.5单位/毫升的Ⅱ型干扰素制剂比400单位/毫升的Ⅰ型干扰素更能抑制[³H]胸腺嘧啶核苷的掺入。(对于Ⅰ型和Ⅱ型干扰素,干扰素活性单位定义为在FS - 4培养物中使水疱性口炎病毒产量降低50%的浓度。)此外,虽然10单位/毫升的Ⅱ型干扰素制剂对正常人成纤维细胞有可逆的细胞生长抑制作用,但所测试的转化细胞(HeLa细胞、骨肉瘤细胞、羊膜细胞)出现广泛细胞死亡,因此表明它可能对某些肿瘤细胞有杀细胞作用。看来人Ⅱ型干扰素(或这些制剂中存在的一种因子)可能是一种有效的抗肿瘤剂。