Caravokyri C, Pringle C R, Leppard K N
Department of Biological Sciences, University of Warwick, Coventry, U.K.
J Gen Virol. 1993 Dec;74 ( Pt 12):2819-24. doi: 10.1099/0022-1317-74-12-2819.
The p55 gag gene of simian immunodeficiency virus macaque strain (SIVmac) and the core p27 gag component linked to a synthetic AUG codon have been cloned into adenovirus type 5 vectors to generate either viable E3-replacement or defective E1-replacement viruses. The viruses express the expected SIV proteins in both human and, for the non-defective viruses, monkey cells. A considerable proportion of the p55 produced is exported from the infected cell. These viruses should prove useful both in studies of the immune response to SIV and as components of candidate vaccines aimed specifically at provoking cytotoxic T cell responses.
猿猴免疫缺陷病毒猕猴株(SIVmac)的p55 gag基因以及与合成AUG密码子相连的核心p27 gag组分已被克隆到5型腺病毒载体中,以产生有活力的E3置换病毒或缺陷型E1置换病毒。这些病毒在人类细胞以及(对于无缺陷病毒而言)猴细胞中均表达预期的SIV蛋白。所产生的相当一部分p55从受感染细胞中输出。这些病毒在SIV免疫反应研究以及作为专门旨在激发细胞毒性T细胞反应的候选疫苗组分方面都应证明是有用的。