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恶性疟原虫的抗原变异

Antigenic Variation in Plasmodium falciparum.

作者信息

Petter Michaela, Duffy Michael F

机构信息

Department of Medicine Royal Melbourne Hospital, Peter Doherty Institute, University of Melbourne, 792 Elizabeth Street, Melbourne, VIC, 3010, Australia.

出版信息

Results Probl Cell Differ. 2015;57:47-90. doi: 10.1007/978-3-319-20819-0_3.

Abstract

Plasmodium falciparum is the protozoan parasite that causes most malaria-associated morbidity and mortality in humans with over 500,000 deaths annually. The disease symptoms are associated with repeated cycles of invasion and asexual multiplication inside red blood cells of the parasite. Partial, non-sterile immunity to P. falciparum malaria develops only after repeated infections and continuous exposure. The successful evasion of the human immune system relies on the large repertoire of antigenically diverse parasite proteins displayed on the red blood cell surface and on the merozoite membrane where they are exposed to the human immune system. Expression switching of these polymorphic proteins between asexual parasite generations provides an efficient mechanism to adapt to the changing environment in the host and to maintain chronic infection. This chapter discusses antigenic diversity and variation in the malaria parasite and our current understanding of the molecular mechanisms that direct the expression of these proteins.

摘要

恶性疟原虫是一种原生动物寄生虫,它导致人类中大多数与疟疾相关的发病和死亡,每年造成超过50万人死亡。该疾病症状与寄生虫在红细胞内反复进行的入侵和无性繁殖周期有关。对恶性疟原虫疟疾的部分、非无菌免疫力只有在反复感染和持续接触后才会产生。成功逃避人类免疫系统依赖于红细胞表面和裂殖子膜上展示的大量抗原性多样的寄生虫蛋白,这些蛋白会暴露于人类免疫系统。这些多态性蛋白在无性繁殖的寄生虫世代之间的表达转换提供了一种有效机制,以适应宿主不断变化的环境并维持慢性感染。本章讨论疟原虫的抗原多样性和变异,以及我们目前对指导这些蛋白质表达的分子机制的理解。

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