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Development of an anti-drug antibody assay to detect anti-drug antibodies to protein and PEG in a PEGylated molecule

机译:抗药物抗体测定的抗药抗体测定,以检测聚乙二醇化分子中的蛋白质和PEG的抗药物抗体

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Background: PEGylation technology is one of long-acting delivery (LAD) platforms used to increase half-life of protein therapeutics. However, PEGylation of anti-Factor D Fab (PEG-aFD) poses challenges for detecting anti-drug antibody (ADA) to both Fab and polyethylene glycol (PEG) portions. Results: Although the bridging ELISA using traditional assay diluent containing Tween 20 is good for detecting ADA to Fab, it failed to detect ADA to PEG. Instead of only reducing Tween 20 in assay diluent, using a proprietary commercial buffer PEG50-1 as assay diluent successfully enabled the detection of ADA to both Fab and PEG with fit-for-purpose sensitivity and drug tolerance. Conclusion: Identification of appropriate assay diluent is critical for detection of ADA to both Fab and PEG in a PEGylated molecule.
机译:背景:Pegymation技术是用于增加蛋白质治疗剂半衰期的长效递送(LAD)平台之一。 然而,抗因子D Fab(PEG-AFD)的聚乙二醇化构成用于检测抗药物抗体(ADA)到FAB和聚乙二醇(PEG)部分的挑战。 结果:虽然使用含有Tween 20的传统测定稀释剂的桥接ELISA适用于检测ADA至FAB,但它未能检测到PEG的ADA。 使用专有的商业缓冲液PEG50-1作为测定稀释剂仅通过适当的敏感性和药物耐受性和耐受药物耐受性和药物耐受性和药物耐受性和药物耐受性和药物耐受性,而不是仅使用专有的商业缓冲液PEG50-1在测定稀释剂中减少试验稀释剂的吐温。 结论:鉴定适当的测定稀释剂对于在聚乙二醇化分子中检测ADA至FAB和PEG的关键。

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