Soler Eric, Le Saux Agnès, Guinut Frédéric, Passet Bruno, Cohen Ruxandra, Merle Christine, Charpilienne Annie, Fourgeux Cynthia, Sorel Véronique, Piriou Antoine, Schwartz-Cornil Isabelle, Cohen Jean, Houdebine Louis-Marie
Biologie du Développement et de la Reproduction, INRA, bât.440, Jouy-en-Josas, France.
Transgenic Res. 2005 Dec;14(6):833-44. doi: 10.1007/s11248-005-1771-0.
Rotaviruses are the main cause of infantile viral gastroenteritis worldwide leading to approximately 500,000 deaths each year mostly in the developing world. For unknown reasons, live attenuated viruses used in classical vaccine strategies were shown to be responsible for intussusception (a bowel obstruction). New strategies allowing production of safe recombinant non-replicating rotavirus candidate vaccine are thus clearly needed. In this study we utilized transgenic rabbit milk as a source of rotavirus antigens. Individual transgenic rabbit lines were able to produce several hundreds of micrograms per ml of secreted recombinant VP2 and VP6 proteins in their milk. Viral proteins expressed in our model were immunogenic and were shown to induce a significant reduction in viral antigen shedding after challenge with virulent rotavirus in the adult mouse model. To our knowledge, this is the first report of transgenic mammal bioreactors allowing the rapid co-production of two recombinant viral proteins in milk to be used as a vaccine.
轮状病毒是全球婴幼儿病毒性肠胃炎的主要病因,每年导致约50万人死亡,其中大部分发生在发展中世界。由于不明原因,传统疫苗策略中使用的减毒活病毒被证明是肠套叠(一种肠梗阻)的病因。因此,显然需要新的策略来生产安全的重组非复制型轮状病毒候选疫苗。在本研究中,我们利用转基因兔奶作为轮状病毒抗原的来源。单个转基因兔系能够在其乳汁中每毫升产生数百微克分泌型重组VP2和VP6蛋白。在我们的模型中表达的病毒蛋白具有免疫原性,并显示在成年小鼠模型中用强毒轮状病毒攻击后,能显著减少病毒抗原的脱落。据我们所知,这是关于转基因哺乳动物生物反应器在乳汁中快速共同生产两种重组病毒蛋白用作疫苗的首次报道。