Reed S G, Douglass T G, Speer C A
Am J Trop Med Hyg. 1982 Jul;31(4):723-9. doi: 10.4269/ajtmh.1982.31.723.
Macrophages from the peritoneal cavities of normal mice or mice previously immunized with epimastigotes of Trypanosoma cruzi were incubated with sera from normal or immunized mice and then infected with T. cruzi epimastigotes or trypomastigotes. After 2 hours of incubation the specimens were prepared for scanning electron microscopy. Macrophages from immunized mice were observed to be qualitatively and quantitatively more effective in binding either parasite form than were macrophages from normal mice. Preincubation with specific antibody appeared to enhance parasite binding in all cases, and extracellular destruction of both epimastigote and trypomastigote forms was noted in these preparations. While extensive destruction of epimastigotes was seen with either normal or immune macrophages pre-incubated with antibody, lysis of trypomastigotes was typically seen only in the presence of both immune macrophages and specific antibody.
将正常小鼠或先前用克氏锥虫无鞭毛体免疫的小鼠腹腔巨噬细胞与正常或免疫小鼠的血清一起孵育,然后用克氏锥虫无鞭毛体或 trypomastigotes 感染。孵育2小时后,制备标本用于扫描电子显微镜检查。观察到来自免疫小鼠的巨噬细胞在结合任何一种寄生虫形态方面在质量和数量上都比正常小鼠的巨噬细胞更有效。在所有情况下,与特异性抗体预孵育似乎增强了寄生虫结合,并且在这些制剂中注意到无鞭毛体和 trypomastigote 形态的细胞外破坏。虽然在用抗体预孵育的正常或免疫巨噬细胞中都观察到无鞭毛体的广泛破坏,但通常仅在存在免疫巨噬细胞和特异性抗体的情况下才观察到 trypomastigotes 的裂解。