Levy J A, Cheng-Mayer C, Dina D, Luciw P A
Science. 1986 May 23;232(4753):998-1001. doi: 10.1126/science.3010461.
A molecular clone of the AIDS-associated retrovirus (ARV-2) was transfected into human T lymphocyte and monocyte cell lines as well as mouse, mink, monkey, and human fibroblast lines. A replicating virus with cytopathic and biologic properties of ARV-2 was recovered from all the cell lines. The animal and human fibroblast cells are resistant to direct infection by ARV, and in these experiments virus production in the fibroblast lines, especially mouse, was reduced compared to human lymphocytes. However, human fibroblasts were more permissive to virus expression than mouse cells. These results show that, whereas the primary block to ARV infection in certain cells may occur at the cell surface, intracellular mechanisms can also participate in controlling virus replication. The results have relevance to vaccine development and encourage further work with modified molecular clones to examine regions of the ARV genome necessary for cytopathology and replication.
将艾滋病相关逆转录病毒(ARV - 2)的一个分子克隆转染到人类T淋巴细胞和单核细胞系以及小鼠、水貂、猴和人类成纤维细胞系中。从所有细胞系中都回收了具有ARV - 2细胞病变和生物学特性的复制病毒。动物和人类成纤维细胞对ARV的直接感染具有抗性,在这些实验中,与人类淋巴细胞相比,成纤维细胞系(尤其是小鼠成纤维细胞系)中的病毒产量有所降低。然而,人类成纤维细胞比小鼠细胞对病毒表达更具容许性。这些结果表明,虽然在某些细胞中ARV感染的主要障碍可能发生在细胞表面,但细胞内机制也可参与控制病毒复制。这些结果与疫苗开发相关,并鼓励进一步使用修饰的分子克隆进行研究,以检查ARV基因组中细胞病变和复制所需的区域。