Bayne C J, Loker E S, Yui M A, Stephens J A
Parasite Immunol. 1984 Nov;6(6):519-28. doi: 10.1111/j.1365-3024.1984.tb00822.x.
Cellular interactions, leading to cell-mediated cytotoxicity when Biomphalaria glabrata hemocytes encapsulate Schistosoma mansoni sporocysts, have been investigated. Rabbit antibodies (IgG), when bound to antigens on sporocyst surfaces, prevent the normal cytoadherence (CA) of hemocytes from both susceptible and resistant host snails. Since interference with CA occurs with even fixed sporocysts, the effect is not due to IgG stimulated modulation of the parasite surface. Using two antisera with some overlapping specificities, and quantitative immunofluorescent antibody technique (QIFAT), we determined the concentrations of IgG needed to place equivalent amounts of IgG on the sporocysts. At these concentrations, CA was affected differentially, implying that interference was due to the specific antigens bound, and not due simply to the presence of IgG. Also with QIFAT we determined how much F(ab')2 and IgG from anti-sporocyst serum were needed to block an equivalent amount of antigenic determinants from access by whole FITC labelled IgG. Sporocysts whose surface antigens were equally blocked were equally unadherent for hemocytes, supporting the notion that the nature of obscured antigens, and neither the Fc portion nor the larger size of intact IgG protein, was responsible for the effect on CA. These surprising results imply a role for specific antigen binding sites on snail hemocytes.
当光滑双脐螺血细胞包裹曼氏血吸虫子孢子时会引发细胞介导的细胞毒性,这种细胞间相互作用已得到研究。兔抗体(IgG)与子孢子表面抗原结合后,会阻止来自易感和抗性宿主蜗牛的血细胞正常细胞黏附(CA)。由于即使是固定的子孢子也会干扰细胞黏附,所以这种效应并非由于IgG刺激寄生虫表面的调节作用。我们使用两种具有部分重叠特异性的抗血清以及定量免疫荧光抗体技术(QIFAT),确定了在子孢子上放置等量IgG所需的IgG浓度。在这些浓度下,细胞黏附受到不同影响,这意味着干扰是由于结合的特异性抗原,而不仅仅是由于IgG的存在。同样使用QIFAT,我们确定了来自抗子孢子血清的多少F(ab')2和IgG能够阻止等量抗原决定簇被全荧光素异硫氰酸酯标记的IgG识别。表面抗原被同等程度阻断的子孢子对血细胞的黏附性相同,这支持了这样一种观点,即被遮蔽抗原的性质而非完整IgG蛋白的Fc部分或更大尺寸是对细胞黏附产生影响的原因。这些惊人的结果暗示了蜗牛血细胞上特异性抗原结合位点的作用。