Ivermectin-induced cell-dependent lethal effects on litomosoides carinii microfilariae in vitro.

H Zahner, D Schmidtchen
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Abstract

Ivermectin affected the motility of Litomosoides carinii microfilariae in vitro in a dose dependent manner but did not completely immobilize the larvae and had no lethal effects when tested up to a concentration of 1000 ng/ml. However, killing of microfilariae was induced by ivermectin in vitro in the presence of spleen cells of Mastomys coucha or rats within 14 h. Optimum effects occurred at drug levels of 10-100 ng ivermectin/ml. Addition of infection serum led to increased cytotoxicity when compared with normal serum. Pretreatment in vitro of L. carinii microfilariae with ivermectin in cell-free medium and subsequent exposure to spleen cells caused also cytotoxic effects which appeared to be accelerated in comparison with simultaneous exposure of microfilariae to ivermectin and cells. Pretreated microfilariae, injected intravenously into naive M. coucha were rapidly eliminated from the blood of the recipients. These results suggest that the microfilariae become altered by the drug and thus susceptible to cell-mediated cytotoxic effects. Cytotoxicity did not depend on the attachment of cells to L. carinii microfilariae and was also induced when targets and effector cells were separated by membranes impermeable for cells. Thus ivermectin-induced cellular cytotoxicity to L. carinii microfilariae is at least partly mediated by soluble factors released by effective cells.

伊维菌素诱导的体外细胞依赖性对卡氏石蛾微丝的致死作用。
伊维菌素对carinii Litomosoides微丝的体外运动有剂量依赖性,但当浓度达到1000 ng/ml时,没有完全固定幼虫,也没有致死作用。在体外实验中,伊维菌素在乳糜鼠或大鼠脾细胞存在的情况下,能在14 h内杀灭微丝蚴,10-100 ng /ml的剂量下效果最佳。与正常血清相比,添加感染血清导致细胞毒性增加。用伊维菌素在体外无细胞培养基中预处理卡氏乳杆菌微丝,然后暴露于脾脏细胞也会引起细胞毒性作用,与同时暴露于伊维菌素和细胞相比,这种作用似乎要加速。将预处理过的微丝蚴静脉注射到未感染的库查分枝杆菌中,可迅速从受者的血液中清除。这些结果表明,微丝虫被药物改变,因此易受细胞介导的细胞毒性作用的影响。细胞毒性并不依赖于细胞与卡氏乳杆菌微丝的附着,当靶细胞和效应细胞被细胞不透膜分离时也会产生细胞毒性。因此,伊维菌素诱导的对卡氏杆菌微丝的细胞毒性至少部分是由有效细胞释放的可溶性因子介导的。
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