免疫原性
免疫球蛋白E
单克隆抗体
免疫分析
抗体
化学
分子生物学
色谱法
分析灵敏度
生物
医学
免疫学
病理
替代医学
作者
Xiaojie Deng,Yingying Hou,Wenyi Yuan,Hongzhou Yang,Ruowen Guo,Tingting Liu,Yongzhen Liu,Junjiu Xu,Heng Liu,Likun Gong,Qiuping Qin
出处
期刊:Bioanalysis
[Future Science Ltd]
日期:2024-02-22
卷期号:16 (7): 135-148
被引量:2
标识
DOI:10.4155/bio-2023-0191
摘要
Background: DB-1003 is a humanized anti-IgE monoclonal antibody with higher affinity than omalizumab. In the affinity capture elution (ACE)-based bridging electrochemiluminescent immunoassay (ECLIA) for antibodies to DB-1003, monkey serum IgE caused false-positive results. Materials & methods: The target-specific antibody or its F(ab')2 fragment was used to mitigate drug target interference in an ACE-based bridging ECLIA for the detection of anti-DB-1003 antibodies. Results: The sensitivity of the developed assay was at least 100 ng/ml. When the anti-drug antibody concentration was 250 ng/ml, the assay tolerated at least 20.0 μg/ml of the monkey IgE. Conclusion: Incorporating the target-specific antibody or its F(ab')2 fragment can overcome the interference from monkey serum IgE in ACE-based bridging ECLIA for anti-DB-1003 antibody detection.
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