Van Den Steen P E, Deroost K, Geurts N, Heremans H, Van Damme J, Opdenakker G
Laboratory of Immunobiology, Rega Institute for Medical Research--KULeuven, Minderbroedersstraat 10--B 3000 Leuven.
Verh K Acad Geneeskd Belg. 2011;73(1-2):123-51.
Malaria is a global tropical disease causing more than 1 million deaths and 300 million clinical cases every year. It is caused by parasites from the genus Plasmodium and is transmitted by Anopheles mosquitoes. Approximately 3 billion people live in malaria-endemic regions and a majority of them are infected. In this review, we discuss the life cycle of the parasite, the complex interactions with the human host and the ensuing immune reactions and complications. The immune system plays a dual role in malaria, by providing life-saving immunity against the parasite, but also by causing often lethal complications in a number of patients. Cytokines, chemokines and proteases are key players in the immunopathological complications, and we propose immunomodulation with dexamethasone as a promising strategy for the therapy of malaria-associated acute respiratory distress syndrome.
疟疾是一种全球性热带疾病,每年导致超过100万人死亡和3亿例临床病例。它由疟原虫属的寄生虫引起,通过按蚊传播。约30亿人生活在疟疾流行地区,其中大多数人受到感染。在本综述中,我们讨论了寄生虫的生命周期、与人类宿主的复杂相互作用以及随之而来的免疫反应和并发症。免疫系统在疟疾中发挥双重作用,既提供针对寄生虫的救命免疫,也在许多患者中引发往往致命的并发症。细胞因子、趋化因子和蛋白酶是免疫病理并发症的关键因素,我们提出用地塞米松进行免疫调节是治疗疟疾相关急性呼吸窘迫综合征的一种有前景的策略。