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抗血管内皮生长因子(VEGF)药物对研发系统人VEGF定量检测酶联免疫吸附测定(ELISA)试剂盒中VEGF定量的干扰。

Anti-VEGF drug interference with VEGF quantitation in the R&D systems human quantikine VEGF ELISA kit.

作者信息

Sumner Giane, Georgaros Camille, Rafique Ashique, DiCioccio Thomas, Martin Joel, Papadopoulos Nicholas, Daly Thomas, Torri Albert

机构信息

Regeneron Pharmaceuticals, Inc., Tarrytown, NY 10591, USA.

出版信息

Bioanalysis. 2019 Mar;11(5):381-392. doi: 10.4155/bio-2018-0096. Epub 2019 Mar 20.

Abstract

AIM

To evaluate the accuracy of the Quantikine Human VEGF Immunoassay (R&D Systems) in the presence of VEGF inhibitors.

MATERIALS & METHODS: Quantikine VEGF ELISA (R&D), anti-VEGF mAb (R&D), VEGF and aflibercept (Regeneron), ranibizumab and bevacizumab (Genentech).

RESULTS

Binding affinity of anti-VEGF mAb for VEGF was threefold weaker than aflibercept, but 33- and 40-fold stronger than ranibizumab or bevacizumab. Extended incubation of VEGF complexed with inhibitors led to VEGF dissociation from ranibizumab and bevacizumab, but not aflibercept, and subsequent binding by the immunoassay capture antibody. The immunoassay also detected VEGF:ranibizumab and VEGF:bevacizumab complexes but not VEGF:aflibercept complexes.

CONCLUSION

The immunoassay cannot accurately quantitate VEGF in the presence of these VEGF inhibitors as they interfere with the capture and detection of free VEGF.

摘要

目的

评估在存在血管内皮生长因子(VEGF)抑制剂的情况下,Quantikine人VEGF免疫分析(R&D系统)的准确性。

材料与方法

Quantikine VEGF酶联免疫吸附测定(R&D)、抗VEGF单克隆抗体(R&D)、VEGF和阿柏西普(再生元)、雷珠单抗和贝伐单抗(基因泰克)。

结果

抗VEGF单克隆抗体对VEGF的结合亲和力比阿柏西普弱三倍,但比雷珠单抗或贝伐单抗强33倍和40倍。与抑制剂复合的VEGF延长孵育导致VEGF从雷珠单抗和贝伐单抗上解离,但不会从阿柏西普上解离,随后被免疫分析捕获抗体结合。该免疫分析还检测到VEGF:雷珠单抗和VEGF:贝伐单抗复合物,但未检测到VEGF:阿柏西普复合物。

结论

在这些VEGF抑制剂存在的情况下,该免疫分析无法准确定量VEGF,因为它们会干扰游离VEGF的捕获和检测。

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