Beeson James G, Drew Damien R, Boyle Michelle J, Feng Gaoqian, Fowkes Freya J I, Richards Jack S
Burnet Institute for Medical Research and Public Health, 85 Commercial Road, Melbourne, Victoria, Australia Department of Microbiology, Monash University, Clayton, Victoria, Australia Department of Medicine, University of Melbourne, Parkville, Victoria, Australia
Burnet Institute for Medical Research and Public Health, 85 Commercial Road, Melbourne, Victoria, Australia.
FEMS Microbiol Rev. 2016 May;40(3):343-72. doi: 10.1093/femsre/fuw001. Epub 2016 Jan 31.
Malaria accounts for an enormous burden of disease globally, with Plasmodium falciparum accounting for the majority of malaria, and P. vivax being a second important cause, especially in Asia, the Americas and the Pacific. During infection with Plasmodium spp., the merozoite form of the parasite invades red blood cells and replicates inside them. It is during the blood-stage of infection that malaria disease occurs and, therefore, understanding merozoite invasion, host immune responses to merozoite surface antigens, and targeting merozoite surface proteins and invasion ligands by novel vaccines and therapeutics have been important areas of research. Merozoite invasion involves multiple interactions and events, and substantial processing of merozoite surface proteins occurs before, during and after invasion. The merozoite surface is highly complex, presenting a multitude of antigens to the immune system. This complexity has proved challenging to our efforts to understand merozoite invasion and malaria immunity, and to developing merozoite antigens as malaria vaccines. In recent years, there has been major progress in this field, and several merozoite surface proteins show strong potential as malaria vaccines. Our current knowledge on this topic is reviewed, highlighting recent advances and research priorities.
疟疾在全球造成了巨大的疾病负担,其中恶性疟原虫导致的疟疾占多数,间日疟原虫是第二大重要病因,尤其在亚洲、美洲和太平洋地区。在疟原虫感染期间,寄生虫的裂殖子形式侵入红细胞并在其中复制。正是在感染的血液阶段发生疟疾,因此,了解裂殖子入侵、宿主对裂殖子表面抗原的免疫反应,以及通过新型疫苗和治疗方法靶向裂殖子表面蛋白和入侵配体,一直是重要的研究领域。裂殖子入侵涉及多种相互作用和事件,并且在入侵之前、期间和之后,裂殖子表面蛋白会发生大量加工。裂殖子表面高度复杂,向免疫系统呈现多种抗原。这种复杂性已证明对我们理解裂殖子入侵和疟疾免疫以及开发裂殖子抗原作为疟疾疫苗的努力构成挑战。近年来,该领域取得了重大进展,几种裂殖子表面蛋白显示出作为疟疾疫苗的强大潜力。本文综述了我们目前在这一主题上的知识,突出了近期进展和研究重点。