Stanisic Danielle I, Good Michael F
Institute for Glycomics, Griffith University, Gold Coast Campus, Parklands Drive, Southport, Queensland 4222, Australia.
Vaccine. 2015 Dec 22;33(52):7469-75. doi: 10.1016/j.vaccine.2015.09.057. Epub 2015 Oct 1.
Despite a century of research focused on the development and implementation of effective control strategies, infection with the malaria parasite continues to result in significant morbidity and mortality worldwide. An effective malaria vaccine is considered by many to be the definitive solution. Yet, after decades of research, we are still without a vaccine that is capable of inducing robust, long lasting protection in naturally exposed individuals. Extensive sub-unit vaccine development focused on the blood stage of the malaria parasite has thus far yielded disappointing results. There is now a renewed focus on whole parasite vaccine strategies, particularly as they may overcome some of the inherent weaknesses deemed to be associated with the sub-unit approach. This review discusses the whole parasite vaccine strategy focusing on the blood stage of the malaria parasite, with an emphasis on recent advances and challenges in the development of killed and live attenuated vaccines.
尽管一个世纪以来的研究都聚焦于有效控制策略的开发与实施,但疟原虫感染在全球范围内仍导致了严重的发病和死亡情况。许多人认为有效的疟疾疫苗是最终的解决方案。然而,经过数十年的研究,我们仍未找到一种能够在自然暴露个体中诱导强大、持久保护作用的疫苗。迄今为止,针对疟原虫血液阶段的广泛亚单位疫苗开发取得的结果令人失望。现在人们重新将重点放在全寄生虫疫苗策略上,特别是因为它们可能克服一些被认为与亚单位方法相关的固有弱点。本综述讨论了针对疟原虫血液阶段的全寄生虫疫苗策略,重点是灭活疫苗和减毒活疫苗开发方面的最新进展和挑战。