Widman Douglas G, Ishikawa Tomohiro, Fayzulin Rafik, Bourne Nigel, Mason Peter W
Department of Microbiology and Immunology, University of Texas Medical Branch (UTMB), Galveston, TX 77555, USA.
Vaccine. 2008 May 23;26(22):2762-71. doi: 10.1016/j.vaccine.2008.03.009. Epub 2008 Mar 31.
Safer vaccines are needed to prevent flavivirus diseases. To help develop these products we have produced a pseudoinfectious West Nile virus (WNV) lacking a functional C gene which we have named RepliVAX WN. Here we demonstrate that RepliVAX WN can be safely propagated at high titer in BHK cells and vaccine-certified Vero cells engineered to stably express the C protein needed to trans-complement RepliVAX WN growth. Using these BHK cells we selected a better growing mutant RepliVAX WN population and used this to generate a second-generation RepliVAX WN (RepliVAX WN.2). RepliVAX WN.2 grown in these C-expressing cell lines safely elicit strong protective immunity against WNV disease in mice and hamsters. Taken together, these results indicate the clinical utility of RepliVAX WN.2 as a vaccine candidate against West Nile encephalitis.
需要更安全的疫苗来预防黄病毒疾病。为了帮助开发这些产品,我们制备了一种缺乏功能性C基因的伪感染性西尼罗河病毒(WNV),我们将其命名为RepliVAX WN。在此我们证明,RepliVAX WN可以在BHK细胞和经过疫苗认证的、经基因工程改造以稳定表达反式互补RepliVAX WN生长所需C蛋白的Vero细胞中以高滴度安全繁殖。利用这些BHK细胞,我们筛选出了生长更好的突变型RepliVAX WN群体,并以此制备出了第二代RepliVAX WN(RepliVAX WN.2)。在这些表达C蛋白的细胞系中培养的RepliVAX WN.2能在小鼠和仓鼠中安全地引发针对西尼罗河病毒疾病的强大保护性免疫。综上所述,这些结果表明RepliVAX WN.2作为一种抗西尼罗河脑炎疫苗候选物的临床应用价值。