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Construction of an immunotoxin via site-specific conjugation of anti-Her2 IgG and engineered Pseudomonas exotoxin A

机译:通过抗-Her2 IgG和工程假单胞菌外毒素A的位点特异性结合构建免疫毒素

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摘要

BackgroundImmunotoxins consisting of a toxin from bacteria or plants and a targeting module have been developed as potent anti-cancer therapeutics. The majority of them, especially those in preclinical or clinical testing stages, are fusion proteins of a toxin and antibody fragment. Immunotoxins based on full-length antibodies are less studied, even though the fragment crystallizable (Fc) domain plays an important role in regulating the concentration of immunoglobulin G (IgG) in the serum and in antibody-mediated immune responses against pathogens.
机译:背景技术由细菌或植物的毒素和靶向模块组成的免疫毒素已被开发为有效的抗癌治疗剂。它们中的大多数,尤其是处于临床前或临床测试阶段的那些,是毒素和抗体片段的融合蛋白。尽管可结晶片段(Fc)结构域在调节血清中免疫球蛋白G(IgG)的浓度以及抗体介导的针对病原体的免疫反应中起着重要作用,但基于全长抗体的免疫毒素研究较少。

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