
Simultaneous determination of α‐fetoprotein immune complexes and α‐fetoprotein concentration in hepatocellular carcinoma using dual‐label time‐resolved immunofluorometric assays
Author(s) -
Sheng Shi Le,
Wang Qing,
Huang Gang,
Yu Bin,
Qin Wen Xin
Publication year - 2009
Publication title -
journal of clinical laboratory analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.536
H-Index - 50
eISSN - 1098-2825
pISSN - 0887-8013
DOI - 10.1002/jcla.20316
Subject(s) - hepatocellular carcinoma , alpha fetoprotein , medicine , immunoassay , antibody , monoclonal antibody , carcinoma , pathology , gastroenterology , immunology
α‐Fetoprotein (AFP) is a commonly used tumor marker in the detection of hepatocellular carcinoma (HCC), and its sensitivity and specificity is insufficient to detect HCC in all patient samples. Recently, the immunocomplexed forms of AFP (AFP‐IgM) have been reported to be present in HCC patients. This study was aimed at developing a novel time‐resolved immunofluorometric assay (TR‐IFMA) for the simultaneous determination of AFP‐IgM and AFP concentration in HCC. We constructed a double‐label assay by using Sm 3+ ‐labeled mAb to human IgM antibody, Eu 3+ ‐labeled mAb to AFP, and immobilized another mAb to AFP on the solid phase. The performances of the assay were all found to be satisfactory. The validity of the novel assay was confirmed by the good correlation between the results obtained by TR‐IFMA and commercial ELISA or electrochemiluminescence immunoassay. AFP‐IgM and AFP were increased above the cutoffs in 65.25 and 45.76% of HCC, respectively. ROC analysis yielded the following area under the curve: AFP‐IgM 0.774 (CI 95% 0.736–0.809), AFP 0.771 (CI 95% 0.733–0.860). The combined use of AFP‐IgM and AFP increased the sensitivity of detection to 72.88% in patients with HCC. These data suggest that the use of a combination of two markers in clinical practice could increase the accuracy of HCC diagnosis. J. Clin. Lab. Anal. 23:179–185, 2009.© 2009 Wiley‐Liss, Inc.