Ruppel A, Rother U, Diesfeld H J
Tropenmed Parasitol. 1984 Mar;35(1):23-8.
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.
研究了新制备的血吸虫童虫在体内通过小鼠补体替代途径被调理的能力。将皮肤血吸虫童虫静脉注射到小鼠体内,随后不久从其肺部回收。经过几分钟的体内停留后,通过免疫荧光检测发现,大多数血吸虫童虫表面的C3b比在体外与小鼠血清孵育相同时间的虫体少得多。在体内停留数小时后,所有血吸虫童虫表面均未检测到C3b沉积。注射前对血吸虫童虫进行辐照或用嘌呤霉素处理,并未改变体外和体内补体沉积的差异。此外,曾短暂通过小鼠的血吸虫童虫,在随后与小鼠血清的体外孵育过程中,其表面沉积小鼠补体的能力大部分丧失。提示新转化的血吸虫童虫与鼠补体C3b的调理作用在体内比在体外效率更低。