Gryzik M, Grzywocz Z, Wasilewska D, Kawiak J, Stachowiak R, Bielecki J, Hoser G
Laboratory of Cytometry, Centre of Postgraduate Medical Education, Warsaw, Poland.
Department of Applied Microbiology, Institute of Microbiology, Faculty of Biology, Warsaw University, Warsaw, Poland.
Int J Immunopathol Pharmacol. 2015 Sep;28(3):329-40. doi: 10.1177/0394632015595778. Epub 2015 Jul 27.
Small B-cell lymphocytic lymphoma/chronic lymphocytic leukemia, which typically affects elderly people, is a group of conditions that are not clinically uniform. It has been suggested that using the combined activity of the monoclonal antibody anti-CD20 (rituximab) and Listeria monocytogenes toxin listeriolysin O (LLO) for this condition could produce an enhanced treatment effect. Here, we tested the effect of the joint activity of rituximab and LLO, which is a cell membrane toxin, in human leukemia cell lines. The human B-leukemia Raji cell line, which expresses CD20, and the T-cell Jurkat cell line, which does not express CD20, for comparison were used in model tests. Cell cytotoxicity of rituximab or LLO and both applied jointly to the cell lines was compared in the presence of human plasma complement. Optimal cytotoxic effects dependent on rituximab or LLO concentration were tested separately. LD50 values were determined and used for optimal application of a mixture of the two factors. The cytotoxic effect on Raji cells of both rituximab and LLO was more than 2.5 times that of LLO alone and 1.5 times that of rituximab alone. At the highest tested concentrations, a mixture of the tested factors had a non-specific cytotoxic effect on the Jurkat cell line, as well. The rituximab and LLO binding sites appear to be in a similar region of the Raji leukemia cell membrane, suggesting an effective interaction of both factors. The joint interaction of these compounds in cell membrane pore formation suggests an explanation for the more effective cytotoxic activity that their combination was observed in this experiment.
小B细胞淋巴细胞性淋巴瘤/慢性淋巴细胞白血病通常影响老年人,是一组临床症状不统一的病症。有人提出,将抗CD20单克隆抗体(利妥昔单抗)和单核细胞增生李斯特菌毒素溶细胞素O(LLO)联合用于治疗这种疾病可能会产生增强的治疗效果。在此,我们测试了利妥昔单抗和作为细胞膜毒素的LLO联合作用对人白血病细胞系的影响。在模型测试中,使用了表达CD20的人B淋巴细胞白血病Raji细胞系和不表达CD20的T淋巴细胞Jurkat细胞系进行比较。在存在人血浆补体的情况下,比较了利妥昔单抗或LLO以及两者联合应用于细胞系的细胞毒性。分别测试了依赖于利妥昔单抗或LLO浓度的最佳细胞毒性作用。测定LD50值并用于两种因子混合物的最佳应用。利妥昔单抗和LLO对Raji细胞的细胞毒性作用均分别是单独使用LLO时的2.5倍以上和单独使用利妥昔单抗时的1.5倍以上。在测试的最高浓度下,测试因子的混合物对Jurkat细胞系也有非特异性细胞毒性作用。利妥昔单抗和LLO的结合位点似乎在Raji白血病细胞膜的相似区域,表明两种因子有有效的相互作用。这些化合物在细胞膜孔形成中的联合相互作用为在本实验中观察到的它们组合时更有效的细胞毒性活性提供了解释。