Hudler H, Scheiner O, Stemberger H, Kollaritsch H, Wiedermann G
Tropenmed Parasitol. 1984 Mar;35(1):5-8.
The time dependency of the cytotoxic action of E. histolytica against tissue culture cells of mammalian origin was assessed in a 51Cr-release assay. Obviously, the amebae-dependent cytotoxic activity within the first 30-60 min of the assay against K562 (an erythroleukemic cell line) and MH1C1 (a rat hepatoma cell line) correlated with the pathogenicity of the respective amebae in vivo as measured by the hamster liver infectivity test. The in vivo apathogenic strain of E. histolytica (HK9) exhibited a delayed cytotoxic action in comparison with the in vivo pathogenic strain (SFL3), which revealed approximately 50% of maximum 51Cr-release after 10 min of the assay. Peripheral blood lymphocytes and HeLa cells proved to be not suitable to discriminate between pathogenic and apathogenic strains in vitro. Human antibodies directed against E. histolytica were capable of inhibiting the cytotoxic action of pathogenic amebae against K562 and MH1C1 within the first 30-60 min of the assay, revealing a kinetic pattern nearly identical with that observed with apathogenic amebae against K562. Possibly, this antibody-mediated inhibition of the cytotoxic action of E. histolytica against target cells reflects one of the defence mechanisms of the host against invasive amebiasis.
在一项⁵¹Cr释放试验中评估了溶组织内阿米巴对哺乳动物来源的组织培养细胞的细胞毒性作用的时间依赖性。显然,在试验的最初30 - 60分钟内,针对K562(一种红白血病细胞系)和MH1C1(一种大鼠肝癌细胞系)的依赖于阿米巴的细胞毒性活性与通过仓鼠肝脏感染性试验测量的相应阿米巴在体内的致病性相关。与体内致病菌株(SFL3)相比,溶组织内阿米巴的体内无致病菌株(HK9)表现出延迟的细胞毒性作用,在试验10分钟后,SFL3菌株显示出约50%的最大⁵¹Cr释放。外周血淋巴细胞和HeLa细胞被证明不适合在体外区分致病和无致病菌株。针对溶组织内阿米巴的人抗体能够在试验的最初30 - 60分钟内抑制致病阿米巴对K562和MH1C1的细胞毒性作用,揭示出与无致病阿米巴对K562观察到的动力学模式几乎相同。可能,这种抗体介导的对溶组织内阿米巴对靶细胞的细胞毒性作用的抑制反映了宿主针对侵袭性阿米巴病的防御机制之一。