Bijker Else M, Borrmann Steffen, Kappe Stefan H, Mordmüller Benjamin, Sack Brandon K, Khan Shahid M
Radboud University Medical Center, Department of Medical Microbiology, PO Box 9101, 6500 HB Nijmegen, The Netherlands.
Institute for Tropical Medicine, University of Tübingen, Tübingen, Germany; German Centre for Infection Research, University of Tübingen, Tübingen, Germany; Kenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi, Kenya.
Vaccine. 2015 Dec 22;33(52):7462-8. doi: 10.1016/j.vaccine.2015.09.095. Epub 2015 Oct 23.
The parasitic disease malaria threatens more than 3 billion people worldwide, resulting in more than 200 million clinical cases and almost 600,000 deaths annually. Vaccines remain crucial for prevention and ultimately eradication of infectious diseases and, for malaria, whole sporozoite based immunization has been shown to be the most effective in experimental settings. In addition to immunization with radiation-attenuated sporozoites, chemoprophylaxis and sporozoites (CPS) is a highly efficient strategy to induce sterile protection in humans. Genetically attenuated parasites (GAP) have demonstrated significant protection in rodent studies, and are now being advanced into clinical testing. This review describes the existing pre-clinical and clinical data on CPS and GAP, discusses recent developments and examines how to transform these immunization approaches into vaccine candidates for clinical development.
寄生虫病疟疾威胁着全球超过30亿人,每年导致超过2亿例临床病例和近60万人死亡。疫苗对于预防乃至根除传染病仍然至关重要,对于疟疾而言,基于全子孢子的免疫在实验环境中已被证明是最有效的。除了用辐射减毒子孢子进行免疫外,化学预防和子孢子(CPS)是在人类中诱导无菌保护的高效策略。基因减毒寄生虫(GAP)在啮齿动物研究中已显示出显著的保护作用,目前正在推进到临床试验阶段。本综述描述了关于CPS和GAP的现有临床前和临床数据,讨论了最近的进展,并研究了如何将这些免疫方法转化为用于临床开发的候选疫苗。