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Generation of Anti-Idiotype scFv for Pharmacokinetic Measurement in Lymphoma Patients Treated with Chimera Anti-CD22 Antibody SM03

机译:嵌合体抗CD22抗体SM03治疗的淋巴瘤患者的药代动力学测量抗独特型scFv的产生

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摘要

Pre-clinical and clinical studies of therapeutic antibodies require highly specific reagents to examine their immune responses, bio-distributions, immunogenicity, and pharmacodynamics in patients. Selective antigen-mimicking anti-idiotype antibody facilitates the assessment of therapeutic antibody in the detection, quantitation and characterization of antibody immune responses. Using mouse specific degenerate primer pairs and splenocytic RNA, we generated an idiotype antibody-immunized phage-displayed scFv library in which an anti-idiotype antibody against the therapeutic chimera anti-CD22 antibody SM03 was isolated. The anti-idiotype scFv recognized the idiotype of anti-CD22 antibody and inhibited binding of SM03 to CD22 on Raji cell surface. The anti-idiotype scFv was subsequently classified as Ab2γ type. Moreover, our results also demonstrated firstly that the anti-idiotype scFv could be used for pharmacokinetic measurement of circulating residual antibody in lymphoma patients treated with chimera anti-CD22 monoclonal antibody SM03. Of important, the present approach could be easily adopted to generate anti-idiotype antibodies for therapeutic antibodies targeting membrane proteins, saving the cost and time for producing a soluble antigen.
机译:治疗性抗体的临床前和临床研究需要高度特异性的试剂来检查其在患者中的免疫反应,生物分布,免疫原性和药效学。选择性模仿抗原的抗独特型抗体有助于在抗体免疫反应的检测,定量和表征中评估治疗性抗体。使用小鼠特异性简并引物对和脾细胞RNA,我们生成了独特型抗体免疫的噬菌体展示scFv文库,其中分离了针对治疗性嵌合抗CD22抗体SM03的抗独特型抗体。抗独特型scFv识别抗CD22抗体的独特型,并抑制SM03与Raji细胞表面上的CD22结合。抗独特型scFv随后被分类为Ab2γ型。此外,我们的结果还首先证明,抗独特型scFv可用于在用嵌合抗CD22单克隆抗体SM03治疗的淋巴瘤患者中循环残留抗体的药代动力学测量。重要的是,可以容易地采用本方法来产生针对膜蛋白的治疗性抗体的抗独特型抗体,从而节省了生产可溶性抗原的成本和时间。

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