Stem Cell & Molecular Biology Laboratory, Department of Biotechnology, Indian Institute of Technology Madras, Chennai 600036, India.
J Biotechnol. 2010 Jul 20;148(2-3):147-55. doi: 10.1016/j.jbiotec.2010.04.006. Epub 2010 May 24.
Immunotoxins are fusion proteins of modified toxin conjugated to tumor cell selective ligand. Denileukin diftitox approved by FDA for treatment of CTCL is diphtheria toxin (DT)/IL2 fusion protein targeted to high affinity IL2R. Here, we have attempted to target the more uniquely expressed low affinity IL2R (IL2Ralpha). We designed four immunotoxins, SPRSV1 was designed to code for a single protein of DT (390) and IL2 (133) without any extra amino acids at the junction. SPRSV2 was designed to selectively target low affinity IL2R, it codes for DT (390) and IL2 (69). We also constructed SPRSV3 encoding for only DT (390) without any ligand, as negative control and SPRSV4 was designed similar to commercial equivalent denileukin diftitox, it codes for DT (387) and IL2 (133) with His at the junction. The cytotoxic activities of these immunotoxins were tested in various cell lines, cell lines lacking IL2R expression and healthy MNC were used as controls. The activities of SPRSV1 and SPRSV2 were comparable to that of SPRSV4. SPRSV2 exhibited potent cytotoxicity effectively targeted to alpha subunit of IL2R on various leukemia cell lines. Our studies also showed a negative correlation between CD25 expression and percentage cell viability after treatment with immunotoxins.
免疫毒素是经修饰的毒素与肿瘤细胞选择性配体偶联而成的融合蛋白。FDA 批准用于治疗 CTCL 的地尼白介素二呋替毒素是一种针对高亲和力 IL2R 的白喉毒素 (DT)/IL2 融合蛋白。在这里,我们试图靶向表达更独特的低亲和力 IL2R(IL2Ralpha)。我们设计了四种免疫毒素,SPRSV1 设计用于编码无任何连接区额外氨基酸的 DT(390)和 IL2(133)的单个蛋白。SPRSV2 设计用于选择性靶向低亲和力 IL2R,它编码 DT(390)和 IL2(69)。我们还构建了编码仅 DT(390)而无任何配体的 SPRSV3,作为阴性对照,SPRSV4 的设计类似于商业等效的地尼白介素二呋替毒素,它编码 DT(387)和 IL2(133),在连接处有 His。这些免疫毒素的细胞毒性在各种细胞系中进行了测试,缺乏 IL2R 表达的细胞系和健康的 MNC 用作对照。SPRSV1 和 SPRSV2 的活性与 SPRSV4 相当。SPRSV2 对各种白血病细胞系上的 IL2Rα亚基表现出有效的靶向和强大的细胞毒性。我们的研究还表明,在用免疫毒素治疗后,CD25 表达与细胞存活率之间呈负相关。