Humanized Mouse Models for the Study of Human Malaria Parasite Biology, Pathogenesis, and immunity

被引:48
作者
Minkah, Nana K. [1 ]
Schafer, Carola [1 ]
Kappe, Stefan H. I. [1 ,2 ]
机构
[1] Ctr Infect Dis Res, Seattle, WA 98109 USA
[2] Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA
关键词
Plasmodium falciparum; humanized mouse models; FRG human hepatocyte; human immune system mice; malaria vaccines; LIVER-STAGE DEVELOPMENT; PLASMODIUM-FALCIPARUM; IN-VIVO; MONOCLONAL-ANTIBODIES; RODENT MALARIA; INNATE IMMUNITY; HOST-CELLS; INFECTION; MICE; IMMUNIZATION;
D O I
10.3389/fimmu.2018.00807
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Malaria parasite infection continues to inflict extensive morbidity and mortality in resource-poor countries. The insufficiently understood parasite biology, continuously evolving drug resistance and the lack of an effective vaccine necessitate intensive research on human malaria parasites that can inform the development of new intervention tools. Humanized mouse models have been greatly improved over the last decade and enable the direct study of human malaria parasites in vivo in the laboratory. Nevertheless, no small animal model developed so far is capable of maintaining the complete life cycle of Plasmodium parasites that infect humans. The ultimate goal is to develop humanized mouse systems in which a Plasmodium infection closely reproduces all stages of a parasite infection in humans, including pre-erythrocytic infection, blood stage infection and its associated pathology, transmission as well as the human immune response to infection. Here, we discuss current humanized mouse models and the future directions that should be taken to develop next-generation models for human malaria parasite research.
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页数:10
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