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I-STOD: a new standardization method for analysing indirect-ELISA results of a schistosomiasis field study

Published online by Cambridge University Press:  11 February 2008

J. LUO
Affiliation:
Department of Mathematics and Computer Science, Nanjing Medical University, Nanjing, Jiangsu, 210029, PRChina
J. XU
Affiliation:
Department of Pathogen Biology, Nanjing Medical University, Nanjing, Jiangsu, 210029, PRChina
Y. ZHANG
Affiliation:
Department of Pathogen Biology, Nanjing Medical University, Nanjing, Jiangsu, 210029, PRChina
H. SHAN
Affiliation:
Department of Pathogen Biology, Nanjing Medical University, Nanjing, Jiangsu, 210029, PRChina
S. ZHANG
Affiliation:
Department of Pathogen Biology, Nanjing Medical University, Nanjing, Jiangsu, 210029, PRChina
M. ZHANG
Affiliation:
Department of Pathogen Biology, Nanjing Medical University, Nanjing, Jiangsu, 210029, PRChina
X. TU
Affiliation:
Department of Mathematics and Computer Science, Nanjing Medical University, Nanjing, Jiangsu, 210029, PRChina
M. JI
Affiliation:
Department of Pathogen Biology, Nanjing Medical University, Nanjing, Jiangsu, 210029, PRChina
F. CHEN
Affiliation:
Department of Epidemiology and Statistics, Nanjing Medical University, Nanjing, Jiangsu, 210029, PRChina
P. M. KNOPF
Affiliation:
Center for International Health Research, Rhode Island Hospital, Providence, RI02903, USA Emeritus Prof. of Medical Science, Department of Molecular Microbiology and Immunology, Brown University, Providence, RI02912, USA
J. KURTIS
Affiliation:
Center for International Health Research, Rhode Island Hospital, Providence, RI02903, USA
G. WU
Affiliation:
Department of Pathogen Biology, Nanjing Medical University, Nanjing, Jiangsu, 210029, PRChina
H.-W. WU*
Affiliation:
Department of Pathogen Biology, Nanjing Medical University, Nanjing, Jiangsu, 210029, PRChina
*
*Corresponding author: Department of Pathogen Biology, Nanjing Medical University, Nanjing, Jiangsu, 210029, PRChina. Tel: +86 25 86862793. Fax: +86 25 86862793. E-mail: haiwei@njmu.edu.cn, Haiwei_Wu@Brown.edu

Summary

Variability among samples analysed using the same ELISA protocol generates ambiguity in deciding which assay best quantifies the protein concentration. In this study, we propose a standardization method, called I-STOD (Improved STandardization method for Optical Density), for the transformation of OD values on different plates into relative concentrations of the antibody levels being assessed. We derived an equation relating OD values of different test samples to antibody levels according to the multi-stage reaction dynamics of the indirect-ELISA. Using serum samples from a Schistosomiasis japonica endemic area, we evaluated the fitness of the I-STOD model to experimental data of a standard reference serum in comparison with 5 other models. Calibration curves fitted by the I-STOD method judged to be superior, based on adjusted R2 (adjusted R2>0·99 on 22 out of 26 plates) values. The CV (coefficient of variation) value of the results between multi-well plates and the number of plates with OD values beyond the control range in Shewhart charts also demonstrate that the I-STOD method is a powerful tool which can greatly improve the comparability of results on different multi-well ELISA plates. We conclude that a standardization method is certainly necessary for antibody levels detected in order to properly illustrate clinical differences.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 2008

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References

REFERENCES

Dudley, R. A., Edwards, P., Ekins, R. P., Finney, D. J., Mckenzie, I. G., Raab, G. M., Rodbard, D. and Rodgers, R. P. (1985). Guidelines for immunoassay data processing. Clinical Chemistry 31, 12641271.Google Scholar
Finney, D. J. (1976). Radioligand assay. Biometrics 32, 721740.Google Scholar
Henry, R. J. and Segalove, M. (1952). The running of standards in clinical chemistry and the use of the control chart. Journal of Clinical Pathology 5, 305311. doi: 10.1136/jcp.5.4.305Google Scholar
Karpinski, K. F., Hayward, S. and Tryphonas, H. (1987). Statistical considerations in the quantitation of serum immunoglobulin levels using the enzyme-linked immunosorbent assay (ELISA). Journal of Immunological Methods 103, 189194.Google Scholar
Kortlandt, W., Endeman, H. J. and Hoeke, J. O. (1987). A three-parameter Langmuir-type model for fitting standard curves of sandwich enzyme immunoassays with special attention to the alpha-fetoprotein assay. Analytical Biochemistry 162, 510.Google Scholar
Levey, S. and Jennings, E. R. (1950). The use of control charts in the clinical laboratory. American Journal of Clinical Pathology 20, 10591066.Google Scholar
Neyer, L., Hiller, J., Gish, K., Keller, S. and Caras, I. (2006). Confirming human antibody responses to a therapeutic monoclonal antibody using a statistical approach. Journal of Immunological Methods 315, 8087.Google Scholar
Noor Azian, M. Y., Hakim, S. L., Sumiati, A. and Norhafizah, M. (2006). Seroprevalence of cysticercosis in a rural village of Ranau, Sabah, Malaysia. Southeast Asian Journal of Tropical Medicine and Public Health 37, 5861.Google Scholar
Okuma, Y., Saito, K., O'Connor, A. E., Phillips, D. J., De Kretser, D. M. and Hedger, M. P. (2005). Reciprocal regulation of activin A and inhibin B by interleukin-1 (IL-1) and follicle-stimulating hormone (FSH) in rat Sertoli cells in vitro. Journal of Endocrinology 185, 99110. doi: 10.1677/joe.1.06053.Google Scholar
Plikaytis, B. D., Goldblatt, D., Frasch, C. E., Blondeau, C., Bybel, M. J., Giebink, G. S., Jonsdottir, I., Kayhty, H., Konradsen, H. B., Madore, D. V., Nahm, M. H., Schulman, C. A., Holder, P. F., Lezhava, T., Elie, C. M. and Carlone, G. M. (2000). An analytical model applied to a multicenter pneumococcal enzyme-linked immunosorbent assay study. Journal of Clinical Microbiology 38, 20432050.Google Scholar
Plikaytis, B. D., Turner, S. H., Gheesling, L. L. and Carlone, G. M. (1991). Comparisons of standard curve-fitting methods to quantitate Neisseria meningitidis group A polysaccharide antibody levels by enzyme-linked immunosorbent assay. Journal of Clinical Microbiology 29, 14391446.Google Scholar
Van Gool, T., Vetter, H., Vervoort, T., Doenhoff, M. J., Wetsteyn, J. and Overbosch, D. (2002). Serodiagnosis of imported schistosomiasis by a combination of a commercial indirect hemagglutination test with Schistosoma mansoni adult worm antigens and an enzyme-linked immunosorbent assay with S. mansoni egg antigens. Journal of Clinical Microbiology 40, 34323437. doi: 10.1128/JCM.40.9.3432-3437.2002Google Scholar
Vestergaard, E. M., Poulsen, S. S., Gronbaek, H., Larsen, R., Nielsen, A. M., Ejskjaer, K., Clausen, J. T., Thim, L. and Nexo, E. (2002). Development and evaluation of an ELISA for human trefoil factor 3. Clinical Chemistry 48, 16891695.Google Scholar
Wernette, C. M., Frasch, C. E., Madore, D., Carlone, G., Goldblatt, D., Plikaytis, B., Benjamin, W., Quataert, S. A., Hildreth, S., Sikkema, D. J., Kayhty, H., Jonsdottir, I. and Nahm, M. H. (2003). Enzyme-linked immunosorbent assay for quantitation of human antibodies to pneumococcal polysaccharides. Clinical and Diagnostic Laboratory Immunology 10, 514519. doi: 10.228/CDLI.10.4.514-519.2003Google Scholar
Wu, H., Luo, J. and Wu, G. (1995). A method for the standardization of OD value for the study of schistosome antibody with ELISA. Acta Parasitology et Medica Entomologica Sinica. 2, 140145.Google Scholar
Wu, J. T., Dreger, S., Chow, E. Y. and Bowlby, E. E. (2002). Validation of 2 commercial Neospora caninum antibody enzyme linked immunosorbent assays. Canadian Journal of Veterinary Research 66, 264271.Google Scholar
Zhang, Z., Wu, H.Chen, S., Hu, L., Xie, Z., Qiu, Y., Su, C., Cao, J. P., Wu, Y., Zhang, S. and Wu, G. (1997). Association between IgE antibody against soluble egg antigen and resistance reinfection with Schistosoma japonicum. Transactions of the Royal Society of Tropical Medicine and Hygiene 91, 606608.Google Scholar