Ruppel A, Rother U, Vongerichten H, Diesfeld H J
Parasitology. 1983 Aug;87 (Pt 1):75-86. doi: 10.1017/s0031182000052434.
Living Schistosoma mansoni of various developmental stages were studied with respect to their ability to activate the complement system in sera of humans, mice and rats. Immunofluorescence assays demonstrated that binding of human C3 occurred on fresh schistosomula as well as on schistosomula prepared from mouse lymph-nodes or lungs and on adult schistosomes. However, rodent C3 was deposited only on fresh schistosomula. Deposition of human C3 on the worms' surface required activation of the complement system. The alternative pathway was shown to be involved in deposition of human C3 on schistosomes of all ages, whereas activation of the classical pathway was demonstrable only with fresh schistosomula. Immunoelectrophoretic studies demonstrated a dose-dependent cleavage of human C3 and conversion of factor B by living adult schistosomes. The results demonstrate that the ability of living schistosomes to activate complement in vitro is dependent not only on their development stage but also on the species of the serum.
对处于不同发育阶段的曼氏血吸虫活体进行了研究,以了解它们激活人、小鼠和大鼠血清中补体系统的能力。免疫荧光分析表明,人C3在新鲜童虫以及从小鼠淋巴结或肺中制备的童虫和成虫上均有结合。然而,啮齿动物C3仅沉积在新鲜童虫上。人C3在虫体表面的沉积需要补体系统的激活。已表明替代途径参与了各年龄段曼氏血吸虫上的人C3沉积,而经典途径的激活仅在新鲜童虫中可检测到。免疫电泳研究表明,活的成虫可使人类C3发生剂量依赖性裂解并使因子B转化。结果表明,活的血吸虫在体外激活补体的能力不仅取决于其发育阶段,还取决于血清的种类。