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首页> 外文期刊>Journal of Immunological Methods >An Affinity Capture Elution (ACE) assay for detection of anti-drug antibody to monoclonal antibody therapeutics in the presence of high levels of drug.
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An Affinity Capture Elution (ACE) assay for detection of anti-drug antibody to monoclonal antibody therapeutics in the presence of high levels of drug.

机译:亲和捕获洗脱(ACE)分析,用于在高水平药物存在下检测针对单克隆抗体治疗剂的抗药物抗体。

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摘要

Monoclonal antibody therapeutics typically have relatively long half-lives and can be dosed at high levels. Although formation of anti-drug antibodies (ADA) is relatively rare, detection of these antibodies can be very difficult in the presence of high circulating levels of drug. Typically these ADA are detected by bridging ELISAs which can be very sensitive to even low levels of drug. We describe an ELISA method based on affinity capture of ADA on solid-phase drug followed by removal of excess free drug, release and transfer of bound ADA and subsequent detection using biotinylated drug. The assay is both sensitive and highly tolerant to free drug with detection of 500 ng/ml of ADA readily achieved in the presence of 500 mug/ml of drug.
机译:单克隆抗体治疗剂通常具有相对较长的半衰期,并且可以高剂量给药。尽管抗药物抗体(ADA)的形成相对较少,但在药物循环水平高的情况下,检测这些抗体可能非常困难。通常,这些ADA是通过桥接ELISA来检测的,即使对于低水平的药物也可能非常敏感。我们描述了一种基于ADA在固相药物上的亲和力捕获,然后去除过量的游离药物,释放和转移结合的ADA以及随后使用生物素化药物进行检测的ELISA方法。该测定法对游离药物既敏感又高度耐受,在存在500杯/毫升药物的情况下可以轻松实现500 ng / ml ADA的检测。

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