曼氏血吸虫:静脉注射到小鼠体内后,失去了血吸虫结合小鼠补体的能力。

Tropenmedizin und Parasitologie Pub Date : 1984-03-01
A Ruppel, U Rother, H J Diesfeld
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引用次数: 0

摘要

研究了新鲜制备的血吸虫在体内通过小鼠补体替代途径被调理的能力。将皮肤血吸虫静脉注射到小鼠体内,不久就从小鼠肺部恢复。在体内停留几分钟后,大多数血吸虫表面的免疫荧光检测到的C3b明显少于在体外与小鼠血清孵育相同时间的蠕虫。在体内停留数小时后,在所有血吸虫上均未检测到C3b的沉积。注射前用血吸虫嘌呤霉素照射或治疗并不改变体外和体内补体沉积的差异。此外,在小鼠体内短暂传代的血吸虫,在随后的小鼠血清体外孵育过程中,失去了在其表面沉积小鼠补体的大部分能力。提示用小鼠补体C3b对新转化血吸虫进行体内活化的效率低于体外活化的效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Schistosoma mansoni: loss of the ability of schistosomula to bind mouse complement following intravenous injection into mice.

The ability of freshly prepared schistosomula to become opsonized by the alternative pathway of mouse complement in vivo was investigated. Skin schistosomula were intravenously injected into mice and recovered shortly afterwards from their lungs. Following an in vivo residency of a few minutes, most schistosomula had considerably less C3b detectable by immunofluorescence on their surface than worms which had been incubated for the same time with mouse serum in vitro. Deposition of C3b was undetectable on all schistosomula following an in vivo residency of a few hours. Irradiation or treatment with puromycin of the schistosomula prior to injection did not alter the difference between in vitro and in vivo complement deposition. Moreover, schistosomula which had been passaged briefly through a mouse, lost most of their ability to deposit mouse complement on their surface during a subsequent in vitro incubation with mouse serum. It is suggested that opsonization of freshly transformed schistosomula with C3b of murine complement is less efficient in vivo than in vitro.

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