利用ifn -γ敲除小鼠在免疫功能低下宿主中建立化疗治疗顽固性弓形虫病的动物模型

U. Belal, K. Norose, H. Mun, Mei Chen, R. Mohamed, A. Ahmed, L. Piao, F. Aosai, A. Yano
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引用次数: 1

摘要

采用定量竞争聚合酶链反应(QC-PCR)方法,对IFN-γ敲除(GKO) BALB/c (B/c)小鼠经口感染形成囊的Fukaya菌株后,经或不经磺胺甲恶唑治疗后的心脏、血液、大脑和小肠中的刚地弓形虫数量进行了评估。经磺胺甲恶唑治疗4周后,小鼠的心脏、血液和大脑均出现弓形虫感染,小肠未见弓形虫感染。弓形虫载量与组织和血液中磺胺甲恶唑浓度无相关性。持续磺胺甲恶唑治疗2个月后,心脏和血液中未检出弓形虫,但在大脑中发现少量寄生虫。因此,我们成功地建立了一种动物模型,通过感染弓形虫的GKO B/c小鼠来评估免疫功能低下宿主的化疗方案。
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AN ANIMAL MODEL FOR ESTABLISHING CHEMOTHERAPY AGAINST INTRACTABLE TOXOPLASMOSIS IN IMMUNOCOMPROMISED HOSTS BY THE USE OF IFN-γ KNOCKOUT MICE
The Toxoplasma gondii number was evaluated by quantitative competitive polymerase chain reaction (QC-PCR) assay with or without sulfamethoxazole treatment in the heart, blood, brain, and small intestine of IFN-γ knockout (GKO) BALB/c (B/c) mice after peroral infection with the cyst-forming Fukaya strain. T. gondii infection was observed in the heart, blood, and brain, but not in the small intestine, of mice treated with sulfamethoxazole for 4 weeks. No correlation between T. gondii loads and sulfamethoxazole concentrations in tissues and blood was observed. T gondii was not detected in the heart and blood after continuous sulfamethoxazole treatment for two months, but a small number of parasites was demonstrated in the brain. Thus, we successfully established an animal model for evaluating chemotherapy regimens in immunocompromised hosts by using GKO B/c mice infected with T. gondii.
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