Joseph M, Capron A, Butterworth A E, Sturrock R F, Houba V
Clin Exp Immunol. 1978 Jul;33(1):48-56.
Normal human blood monocytes, pre-incubated at 37 degrees C with sera from patients infected with Schistosoma mansoni, strongly adhered to S. mansoni schistosomula in vitro, whereas no significant adherence was induced by sera from uninfected individuals. Comparable adherence occurred with normal baboon blood monocytes or peritoneal macrophages when these cells were incubated with sera from S. mansoni-infected baboons. Adherence of macrophages to schistosomula was associated with damage to the larvae, as estimated by a 51Cr release technique. Neither adherence nor cytotoxicity was induced by pre-incubation of the schistosomula, instead of the monocytes, with immune serum. The relevant factor in immune serum was heat-labile, but was not a complement component. Absorption and ultracentrifugation experiments showed that immune complexes, containing S. mansoni-specific IgE antibody and soluble parasite antigens, produced monocyte or macrophage adherence and cytotoxicity. Similar observations have been reported previously in the rat model. Since the production of large amounts of IgE is a predominant feature of schistosome infections in man and experimental animals, it is possible that this new mode of mononuclear phagocyte activation could act as an immune effector mechanism against S. mansoni.
正常人类血液单核细胞在37℃下与曼氏血吸虫感染患者的血清预孵育后,在体外能强烈黏附于曼氏血吸虫童虫,而未感染个体的血清则不会诱导出明显的黏附现象。当正常狒狒血液单核细胞或腹腔巨噬细胞与曼氏血吸虫感染的狒狒血清孵育时,会出现类似的黏附情况。通过51Cr释放技术评估,巨噬细胞对童虫的黏附与幼虫损伤有关。用免疫血清预孵育童虫而非单核细胞,既不会诱导黏附也不会产生细胞毒性。免疫血清中的相关因子对热不稳定,但不是补体成分。吸收和超速离心实验表明,含有曼氏血吸虫特异性IgE抗体和可溶性寄生虫抗原的免疫复合物可产生单核细胞或巨噬细胞的黏附和细胞毒性。先前在大鼠模型中也有类似的观察结果。由于在人类和实验动物中,大量产生IgE是血吸虫感染的一个主要特征,这种单核吞噬细胞激活的新模式有可能作为针对曼氏血吸虫的一种免疫效应机制。