Pasini Erica M, van der Wel Annemarie Voorberg, Heijmans Nicole, Klop Onny, Zeeman Anne-Marie, Oostermeijer Herman, Nieuwenhuis Ivonne, Garcia Roberto Rodriguez, van der Werff Nicole Onur, Hofman Sam O, Verreck Frank A W, Remarque Edmond J, Faber Bart W, Kocken Clemens H M
Department of Parasitology, Biomedical Primate Research Centre, Rijswijk, The Netherlands.
Department of Virology, Biomedical Primate Research Centre, Rijswijk, The Netherlands.
NPJ Vaccines. 2022 Oct 27;7(1):126. doi: 10.1038/s41541-022-00555-0.
Vaccine development for Plasmodium vivax, an important human relapsing malaria, is lagging behind. In the case of the most deadly human malaria P. falciparum, unprecedented high levels of protection have been obtained by immunization with live sporozoites under accompanying chemoprophylaxis, which prevents the onset of blood-stage malaria. Such an approach has not been fully evaluated for relapsing malaria. Here, in the P. cynomolgi-rhesus macaque model for relapsing malaria, we employ the parasites' natural relapsing phenotype to self-boost the immune response against liver-stage parasites, following a single-shot high-dose live sporozoite vaccination. This approach resulted in sterile protection against homologous sporozoite challenge in three out of four animals in the group that was also exposed for several days to blood stages during primary infection and relapses. One out of four animals in the group that received continuous chemoprophylaxis to abort blood-stage exposure was also protected from sporozoite challenge. Although obtained in a small number of animals as part of a Proof-of-Concept study, these results suggest that limited blood-stage parasite exposure may augment protection in this model. We anticipate our data are a starting point for further research into correlates of protection and extrapolation of the single-shot approach to develop efficacious malaria vaccines against relapsing human malaria.
间日疟原虫是一种重要的人类复发性疟疾,针对它的疫苗研发一直滞后。对于最致命的人类疟疾——恶性疟原虫,在进行化学预防以防止血期疟疾发作的同时,通过接种活子孢子免疫已获得了前所未有的高保护水平。但这种方法尚未在复发性疟疾中得到充分评估。在此,在用于复发性疟疾的食蟹猴 - 恒河猴模型中,我们采用寄生虫的自然复发表型,在单次高剂量活子孢子疫苗接种后,自我增强针对肝期寄生虫的免疫反应。这种方法在该组四分之三的动物中产生了针对同源子孢子攻击的无菌保护,这些动物在初次感染和复发期间也有几天暴露于血期。在接受持续化学预防以中止血期暴露的组中,四分之一的动物也受到了子孢子攻击的保护。尽管这些结果是在作为概念验证研究一部分的少数动物中获得的,但这些结果表明,有限的血期寄生虫暴露可能会增强该模型中的保护作用。我们预计我们的数据是进一步研究保护相关因素以及将单次接种方法外推以开发针对人类复发性疟疾的有效疟疾疫苗的起点。