Blalock J E, Stanton G J
J Gen Virol. 1978 Nov;41(2):325-31. doi: 10.1099/0022-1317-41-2-325.
The rate of development of interferon-induced virus resistance in a mixture of two human cell types (U and WISH) is determined by the cell type (WISH) in the mixture which responds first. This phenomenon has been shown with two types of interferon assay procedure, and with both vesicular stomatitis virus and Sindbis virus. The transfer of virus resistance from one human cell (WISH) to another (U) (homospecific transfer) is much more efficient than the transfer from mouse L cells to WISH cells (heterospecific transfer), as shown by a much lower ratio of donor to recipient cells required for maximum transfer as well as a more rapid transfer. Thus, virus protection afforded by the interferon system is amplified more efficiently in mixtures of different human cells than in mixtures of mouse and human cells. These results suggest that, in a mixed population of cells such as occurs in vivo, more slowly responding cells might be influenced by cells which respond more rapidly to interferon. A defensive role is suggested for this mechanism which amplifies protection due to interferon.
在两种人类细胞类型(U细胞和WISH细胞)的混合物中,干扰素诱导的病毒抗性的发展速率由混合物中首先做出反应的细胞类型(WISH细胞)决定。这一现象在两种干扰素检测程序中均有体现,并且在水疱性口炎病毒和辛德毕斯病毒中也得到了证实。如最大转移所需的供体细胞与受体细胞的比例更低以及转移速度更快所示,病毒抗性从一种人类细胞(WISH细胞)转移到另一种人类细胞(U细胞)(同种特异性转移)比从小鼠L细胞转移到WISH细胞(异种特异性转移)效率更高。因此,与小鼠和人类细胞的混合物相比,干扰素系统提供的病毒保护在不同人类细胞的混合物中得到了更有效的放大。这些结果表明,在诸如体内出现的混合细胞群体中,反应较慢的细胞可能会受到对干扰素反应更快的细胞的影响。这种放大干扰素诱导保护作用的机制被认为具有防御作用。