TY - JOUR
T1 - Improvement for identification of heterophile antibody interference and AFP hook effect in immunoassays with multiplex suspension bead array system
AU - Wang, Yajie
AU - Yu, Jinsheng
AU - Ren, Yuan
AU - Liu, Li
AU - Li, Haowen
AU - Guo, Anchen
AU - Shi, Congning
AU - Fang, Fang
AU - Juehne, Twyla
AU - Yao, Jianer
AU - Yang, Enhuan
AU - Zhou, Xuelei
AU - Kang, Xixiong
N1 - Funding Information:
This work was supported by grants from the Beijing Nova Program (# 2008A082 ), the Youth Foundation of Beijing Municipal Health Bureau (# QN2009-010 ), the Beijing Municipal Health System “215” High-level Medical Personnel Culturing Project (# 2011-3-038 ), the Foundation of Science and Technology for Excellent Students Abroad of Beijing City (year of 2013), the Capital Medical University Cooperation Project between Basic Research and Clinical Research (# 11JL07 ), and the Natural Science Foundation of Beijing City (# 7132094 ). All authors have no disclosure of any conflicts of interest.
PY - 2013/11/15
Y1 - 2013/11/15
N2 - Background: A variety of immunoassays including multiplex suspension bead array have been developed for tumor marker detections; however, these assays could be compromised in their sensitivity and specificity by well-known heterophile antibody interference and hook effect. Methods: Using Luminex® multiplex suspension bead arrays, we modified protocols with two newly-developed solutions that can identify heterophile antibody interference and AFP hook effect. Effectiveness of the two solutions was assessed in serum samples from patients. Results: Concentrations of 9 tumor markers in heterophile antibody positive samples assayed with Solution A, containing murine monoclonal antibodies and mouse serum, were significantly reduced when compared with those false high signals assayed without Solution A (all p. <. 0.01). With incorporation of Solution H (fluorescent beads linked with AFP antigen), a new strategy for identification of AFP hook effect was established, and with this strategy AFP hook effect was identified effectively in serum samples with very high levels of AFP. Conclusions: Two proprietary solutions improve the identification of heterophile antibody interference and AFP hook effect. With these solutions, multiplex suspension bead arrays provide more reliable testing results in tumor marker detection where complex clinical serum samples are used.
AB - Background: A variety of immunoassays including multiplex suspension bead array have been developed for tumor marker detections; however, these assays could be compromised in their sensitivity and specificity by well-known heterophile antibody interference and hook effect. Methods: Using Luminex® multiplex suspension bead arrays, we modified protocols with two newly-developed solutions that can identify heterophile antibody interference and AFP hook effect. Effectiveness of the two solutions was assessed in serum samples from patients. Results: Concentrations of 9 tumor markers in heterophile antibody positive samples assayed with Solution A, containing murine monoclonal antibodies and mouse serum, were significantly reduced when compared with those false high signals assayed without Solution A (all p. <. 0.01). With incorporation of Solution H (fluorescent beads linked with AFP antigen), a new strategy for identification of AFP hook effect was established, and with this strategy AFP hook effect was identified effectively in serum samples with very high levels of AFP. Conclusions: Two proprietary solutions improve the identification of heterophile antibody interference and AFP hook effect. With these solutions, multiplex suspension bead arrays provide more reliable testing results in tumor marker detection where complex clinical serum samples are used.
KW - Heterophile antibody
KW - Hook effect
KW - Immunoassay
KW - Multiplex suspension bead array
KW - Tumor marker
UR - http://www.scopus.com/inward/record.url?scp=84884720554&partnerID=8YFLogxK
U2 - 10.1016/j.cca.2013.09.005
DO - 10.1016/j.cca.2013.09.005
M3 - Article
C2 - 24041811
AN - SCOPUS:84884720554
SN - 0009-8981
VL - 426
SP - 68
EP - 74
JO - Clinica Chimica Acta
JF - Clinica Chimica Acta
ER -