Sacci J B, Schriefer M E, Resau J H, Wirtz R A, Detolla L J, Markham R B, Azad A F
University of Maryland School of Medicine, Baltimore 21201.
Proc Natl Acad Sci U S A. 1992 May 1;89(9):3701-5. doi: 10.1073/pnas.89.9.3701.
Research on the exoerythrocytic (EE) stages of human malaria parasites has been hindered because of the lack of an easily available suitable animal model. We report here an approach to produce mature EE-stage Plasmodium falciparum parasites by using severe combined immunodeficient (scid) mice with transplanted human hepatocytes. Transplantation of human hepatocytes into scid mice (scid hu-hep), their subsequent intravenous infection with P. falciparum sporozoites, and the development of mature liver-stage merozoites was achieved. Immunofluorescent staining of scid hu-hep kidney tissue sections demonstrated the presence of circumsporozoite protein (early during infection), merozoite surface antigen 1, and liver schizont antigen 1. The scid hu-hep model can serve as a source of human malaria liver-stage parasites, decreasing the need for nonhuman primates. Use of this model will facilitate characterization of EE-stage antigens and the assessment of stage-specific chemotherapeutic agents and candidate vaccines.
由于缺乏易于获得的合适动物模型,人类疟原虫红细胞外期(EE)的研究受到了阻碍。我们在此报告一种方法,通过将人肝细胞移植到严重联合免疫缺陷(scid)小鼠体内来产生成熟的恶性疟原虫EE期寄生虫。将人肝细胞移植到scid小鼠(scid hu-hep)中,随后用恶性疟原虫子孢子对其进行静脉感染,并实现了成熟肝期裂殖子的发育。scid hu-hep肾组织切片的免疫荧光染色显示存在环子孢子蛋白(感染早期)、裂殖子表面抗原1和肝裂殖体抗原1。scid hu-hep模型可作为人类疟疾肝期寄生虫的来源,减少了对非人灵长类动物的需求。使用该模型将有助于EE期抗原的表征以及阶段特异性化疗药物和候选疫苗的评估。