逃避(道德)
疟疾
生物
疟原虫(生命周期)
寄生虫寄主
恶性疟原虫
免疫系统
多样性(控制论)
人类健康
计算生物学
光学(聚焦)
人命
钥匙(锁)
抗原变异
进化生物学
鉴定(生物学)
寄主(生物学)
生物进化
模式生物
计算机科学
作者
Thayne H. Dickey,Niraj H. Tolia
标识
DOI:10.1146/annurev-micro-042424-032639
摘要
Malaria remains a major global health burden despite decades of effort toward its prevention and treatment. Much of this difficulty stems from the complexity of the Plasmodium parasite's life cycle and its interactions with the human host. Here, we review receptor–ligand interactions between the Plasmodium parasite and human host, with a focus on clinically relevant antigens. The parasite uses a variety of proteins at each stage of its life cycle to achieve requisite functions such as motility, cell traversal, and invasion. In turn, the human immune response targets these key parasite antigens, and we review well-characterized antibody–antigen interactions. Finally, we describe several mechanisms the parasite uses to evade the human immune response. Understanding of this evolutionary back-and-forth has inspired several different vaccines and therapeutics, and we describe ongoing efforts to create improved next-generation versions.
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