Wang Lina, Webster Diane E, Campbell Alison E, Dry Ian B, Wesselingh Steve L, Coppel Ross L
Department of Microbiology, Monash University, Clayton, Vic. 3800, Australia.
Int J Parasitol. 2008 Jan;38(1):103-10. doi: 10.1016/j.ijpara.2007.06.005. Epub 2007 Jul 5.
Malaria is a major global health problem for which effective control measures are urgently needed. Considerable effort has been focused on the development of effective vaccines against the causative parasite and protective vaccine trials are now being reported. Due to the relative poverty and lack of infrastructure in malaria-endemic areas, a successful immunisation strategy will depend critically on cheap and scaleable methods of vaccine production, distribution and delivery. One promising technology is transgenic plants, both as a bioreactor for the vaccine-manufacturing process as well as a matrix for oral immunisation. In this study, we investigated the feasibility of using transgenic plants to induce protective immunity against malaria infection using Plasmodium yoelii merozoite surface protein 4/5 (PyMSP4/5) in a mouse model of malaria infection. Our data show that the PyMSP4/5 protein can be produced in plants in a configuration that reacts with protective antibodies. Optimisation of codon usage for the PyMSP4/5 gene resulted in significantly increased antigen expression in plants. PyMSP4/5 protein from the codon-optimised construct accumulated to 0.25% of total soluble protein, a sixfold increase over the native gene sequence. Tobacco-made PyMSP4/5 was able to induce antigen-specific antibodies in mice following parenteral delivery, as well as boost the antibody responses induced by DNA vaccination when delivered parenterally or orally. We believe this is the first report to show that plant-made malaria antigens are immunogenic. However, the antibody levels were not high enough to protect the immunised mice against a lethal challenge with P. yoelii. Further strategies are needed to achieve a protective dose, including improvements to antigen expression levels in plants and strategies to enhance the immunogenicity of the expressed antigen.
疟疾是一个重大的全球健康问题,迫切需要有效的控制措施。大量努力都集中在研发针对致病寄生虫的有效疫苗上,目前已有关于保护性疫苗试验的报道。由于疟疾流行地区相对贫困且缺乏基础设施,成功的免疫策略将严重依赖于廉价且可扩展的疫苗生产、分发和接种方法。一种有前景的技术是转基因植物,它既可以作为疫苗生产过程的生物反应器,也可以作为口服免疫的载体。在本研究中,我们在疟疾感染小鼠模型中研究了利用转基因植物表达约氏疟原虫裂殖子表面蛋白4/5(PyMSP4/5)来诱导针对疟疾感染的保护性免疫的可行性。我们的数据表明,PyMSP4/5蛋白能够在植物中以与保护性抗体发生反应的形式产生。对PyMSP4/5基因的密码子使用进行优化后,植物中的抗原表达显著增加。来自密码子优化构建体的PyMSP4/5蛋白积累至总可溶性蛋白的0.25%,比天然基因序列增加了六倍。烟草表达的PyMSP4/5在经肠胃外给药后能够在小鼠体内诱导抗原特异性抗体,并且在经肠胃外或口服给药时能够增强DNA疫苗诱导的抗体反应。我们认为这是首次表明植物表达的疟疾抗原具有免疫原性的报告。然而,抗体水平不足以保护免疫小鼠免受约氏疟原虫的致死性攻击。需要进一步的策略来达到保护性剂量,包括提高植物中抗原的表达水平以及增强所表达抗原免疫原性的策略。