[Entamoeba histolytica: II. Effect of humoral immune mechanisms on cytotoxic activity].

Tropenmedizin und Parasitologie Pub Date : 1984-03-01
H Hudler, O Scheiner, H Stemberger, H Kollaritsch, G Wiedermann
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Abstract

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.

溶组织内阿米巴:2;体液免疫机制对细胞毒活性的影响
用51cr释放法测定溶组织杆菌对哺乳动物组织培养细胞的细胞毒作用的时间依赖性。显然,在实验的前30-60分钟内,对K562(一种红白血病细胞系)和MH1C1(一种大鼠肝癌细胞系)的阿米巴依赖的细胞毒活性与仓鼠肝脏感染性试验测量的阿米巴在体内的致病性相关。与体内致病菌株(SFL3)相比,溶组织芽胞杆菌(HK9)的体内致病菌株(HK9)表现出延迟的细胞毒作用,在实验10分钟后显示出约50%的最大51cr释放量。体外实验证明,外周血淋巴细胞和HeLa细胞不适合用于病原菌和致病性菌株的区分。针对溶组织芽胞杆菌的人抗体能够在检测的前30-60分钟内抑制致病性阿米巴对K562和MH1C1的细胞毒作用,显示出与致病性阿米巴对K562的动力学模式几乎相同。可能,这种抗体介导的溶组织芽胞杆菌对靶细胞的细胞毒性作用的抑制反映了宿主对侵袭性阿米巴病的防御机制之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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