Department of Microbiology and Immunology, Weill Medical College of Cornell University, New York, NY 10065; email:
Department of Microbiology and Molecular Genetics, Institute for Medical Research Israel-Canada and Kuvin Center for the Study of Infectious and Tropical Diseases, Hebrew University Hadassah Medical School, Jerusalem 91120, Israel; email:
Annu Rev Microbiol. 2017 Sep 8;71:625-641. doi: 10.1146/annurev-micro-090816-093841. Epub 2017 Jul 11.
Malaria is a significant threat throughout the developing world. Among the most fascinating aspects of the protozoan parasites responsible for this disease are the methods they employ to avoid the immune system and perpetuate chronic infections. Key among these is antigenic variation: By systematically altering antigens that are displayed to the host's immune system, the parasite renders the adaptive immune response ineffective. For Plasmodium falciparum, the species responsible for the most severe form of human malaria, this process involves a complicated molecular mechanism that results in continuously changing patterns of variant-antigen-encoding gene expression. Although many features of this process remain obscure, significant progress has been made in recent years to decipher various molecular aspects of the regulatory cascade that causes chronic infection.
疟疾在发展中国家是一个严重的威胁。引起这种疾病的原生动物寄生虫最吸引人的方面之一是它们用来逃避免疫系统和维持慢性感染的方法。其中关键的是抗原变异:寄生虫通过系统地改变向宿主免疫系统展示的抗原,使适应性免疫反应失效。对于引起最严重人类疟疾的疟原虫,这个过程涉及一个复杂的分子机制,导致变异抗原编码基因表达的模式不断变化。尽管这个过程的许多特征仍然不清楚,但近年来在破译导致慢性感染的调节级联的各个分子方面取得了重大进展。