Rodriguez C R, Fei D T, Keyt B, Baly D L
Department of BioAnalytical Technology, Genetech, South San Francisco, CA 94080, USA.
J Immunol Methods. 1998 Oct 1;219(1-2):45-55. doi: 10.1016/s0022-1759(98)00131-8.
A specific and sensitive fluorometric enzyme-linked immunosorbent assay (ELISA) was developed to measure endogenous levels of vascular endothelial growth factor (VEGF165) in human plasma. The ELISA can be performed in 10% human EDTA plasma, yielding a neat plasma sensitivity of 10 pg/ml or 0.2 pM. The recovery of recombinant human VEGF (rhVEGF) added to human plasma ranges from 89 to 100%. The capture antibody depletes the endogenous signal in normal human plasma, suggesting that the signal is specific for VEGF. The inter-assay and intra-assay coefficients of variation (CV) for the ELISA ranges from 5 to 14% and 8 to 18%, respectively. Characterization of the ELISA using plasmin derived VEGF variants suggests the assay is specific for the VEGF165 isoform. The heterodimer, VEGF(165/110) quantitates similar to that of the intact VEGF165 homodimer, however, the homodimers VEGF121, VEGF110 and the carboxy terminal domain (residues 111-165) are not detected in the assay. Circulating endogenous VEGF levels measured in 50 normal healthy individuals range from 20 to 141 pg/ml, with a mean of 42 +/- 22 pg/ml. There were no significant differences in VEGF levels between males and females. Circulating endogenous VEGF levels in cancer patients ranged from 32 to 418 pg/ml, averaging 129 +/- 17 pg/ml.
开发了一种特异性和灵敏的荧光酶联免疫吸附测定法(ELISA),用于测量人血浆中血管内皮生长因子(VEGF165)的内源性水平。该ELISA可在10%人乙二胺四乙酸(EDTA)血浆中进行,纯血浆灵敏度为10 pg/ml或0.2 pM。添加到人血浆中的重组人VEGF(rhVEGF)回收率在89%至100%之间。捕获抗体可消除正常人血浆中的内源性信号,表明该信号对VEGF具有特异性。该ELISA的批间和批内变异系数(CV)分别为5%至14%和8%至18%。使用纤溶酶衍生的VEGF变体对ELISA进行表征表明,该测定法对VEGF165异构体具有特异性。异二聚体VEGF(165/110)的定量与完整的VEGF165同二聚体相似,然而,在该测定法中未检测到同二聚体VEGF121、VEGF110和羧基末端结构域(残基111-165)。在50名正常健康个体中测得的循环内源性VEGF水平在20至141 pg/ml之间,平均为42±22 pg/ml。男性和女性之间的VEGF水平无显著差异。癌症患者的循环内源性VEGF水平在32至418 pg/ml之间,平均为129±17 pg/ml。