University of Texas Medical Branch, Departments of Microbiology and Immunology and Internal Medicine, Division of Infectious Diseases, 301 University Boulevard, Galveston, TX 77555-0435, USA.
Trends Parasitol. 2012 Feb;28(2):73-82. doi: 10.1016/j.pt.2011.10.006. Epub 2011 Nov 17.
Malaria kills close to a million people every year, mostly children under the age of five. In the drive towards the development of an effective vaccine and new chemotherapeutic targets for malaria, field-based studies on human malaria infection and laboratory-based studies using animal models of malaria offer complementary opportunities to further our understanding of the mechanisms behind malaria infection and pathology. We outline here the parallels between the Plasmodium chabaudi mouse model of malaria and human malaria. We will highlight the contribution of P. chabaudi to our understanding of malaria in particular, how the immune response in malaria infection is initiated and regulated, its role in pathology, and how immunological memory is maintained. We will also discuss areas where new tools have opened up potential areas of exploration using this invaluable model system.
疟疾每年导致近 100 万人死亡,其中大多数是 5 岁以下的儿童。为了开发有效的疟疾疫苗和新的化学治疗靶点,基于现场的人类疟疾感染研究和基于实验室的疟疾动物模型研究为进一步了解疟疾感染和发病机制提供了互补的机会。本文概述了间日疟原虫(Plasmodium chabaudi)小鼠疟疾模型与人类疟疾之间的相似之处。我们将特别强调 P. chabaudi 对我们理解疟疾的贡献,包括疟疾感染中免疫反应的启动和调节、其在发病机制中的作用以及免疫记忆是如何维持的。我们还将讨论新工具在利用这一宝贵模型系统方面开辟了哪些具有探索潜力的新领域。