Weina P J, Burns W C
Department of Zoology, University of Wisconsin-Madison 53706.
J Parasitol. 1992 Apr;78(2):378-80.
In an attempt to find a small animal model for paragonimiasis, Syrian hamsters were infected with between 1 and 16 metacercariae of Paragonimus kellicotti. A definitive mortality dose-response was observed with 90% of all hamsters given 3 or more parasites succumbing to the infection within 35 days. Hamsters demonstrated acute pleuritis, reactive mesothelial hyperplasia, subpleural accumulations of reactive and mature plasma cells, neovascularization, fibrohistiocytic thickening with and without giant cells, raised fibroconnective tissue lesions, and granulomatous inflammation with hemorrhage. Perivascular plasmacytic (lymphocytic) infiltrate, multifocal bronchopneumonia, and parenchymal necrotizing suppurative granulomatous inflammation, hemorrhagic pneumonia, and diffuse sprinkling of eosinophils, neutrophils, and intraalveolar macrophages also were observed. The response observed here may represent a new small animal mortality model useful in the search for new compounds to treat early trematode infections.
为了找到一种肺吸虫病的小动物模型,将1至16条凯氏肺吸虫囊蚴感染叙利亚仓鼠。观察到明确的致死剂量反应,所有感染3个或更多寄生虫的仓鼠中有90%在35天内死于感染。仓鼠表现出急性胸膜炎、反应性间皮增生、反应性和成熟浆细胞的胸膜下积聚、新生血管形成、有或无巨细胞的纤维组织细胞增厚、纤维结缔组织病变隆起以及伴有出血的肉芽肿性炎症。还观察到血管周围浆细胞(淋巴细胞)浸润、多灶性支气管肺炎、实质坏死性化脓性肉芽肿性炎症、出血性肺炎以及嗜酸性粒细胞、中性粒细胞和肺泡内巨噬细胞的弥漫性散在分布。此处观察到的反应可能代表一种新的小动物致死模型,有助于寻找治疗早期吸虫感染的新化合物。