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Clinical and Vaccine Immunology, May 2009, p. 706-711, Vol. 16, No. 5
1071-412X/09/$08.00+0     doi:10.1128/CVI.00425-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Two-Step Epstein-Barr Virus Immunoglobulin A Enzyme-Linked Immunosorbent Assay System for Serological Screening and Confirmation of Nasopharyngeal Carcinoma{triangledown}

Dewi K. Paramita,1 Jajah Fachiroh,1 Sofia M. Haryana,1 and Jaap M. Middeldorp2*

Department of Histology and Cell Biology, Gadjah Mada University, Yogyakarta, Indonesia,1 Department of Pathology, Vrije Universiteit Medical Center, Amsterdam, The Netherlands2

Received 15 November 2008/ Returned for modification 9 January 2009/ Accepted 12 March 2009

Undifferentiated nasopharyngeal carcinoma (NPC; WHO type III) is 100% associated with Epstein-Barr virus (EBV) infection and the fourth most prevalent cancer in Indonesian males. Therapy failure is high, since most patients come to the hospital at an advanced stage of disease. Screening for early-stage NPC is needed. Here, a simple and economical two-step enzyme-linked immunosorbent assay (ELISA) system is proposed for diagnosing NPC in high-risk populations, employing the peptide-based immunoglobulin A (IgA) EBNA1 plus viral capsid antigen p18 ELISA as an initial screening test and the IgA early antigen (EA) ELISA using a different set of EBV antigens as a confirmation test. A total of 151 NPC patients and 199 regional healthy EBV carriers were used to evaluate the two-step ELISA approach. Routinely, EBV IgG immunoblotting is used as a standard confirmation test. The sensitivity and specificity for diagnosing NPC by the two-step ELISA approach increased from 85.4% to 96.7% and 90.1% to 98%, respectively, with positive predictive values and negative predictive values increasing from 78.7 and 93.9% to 97.3 and 97.5%, respectively, relative to the immunoblotting confirmation system. On discrepant samples, additional testing was done by EBV DNA load quantification in blood. Results showed that 5/11 discrepant NPC samples with an elevated IgA EA ELISA also had elevated an EBV DNA load in the circulation (range, 3,200 to 25,820 copies/ml). Therefore, the IgA EA ELISA is proposed as a confirmation test in first-line NPC serological screening studies. This two-step EBV ELISA system provides a standardized approach for NPC screening and may be used in combination with dried blood sampling in future field studies for identification of early-stage NPC in high-risk regions.

* Corresponding author. Mailing address: Department of Pathology, Vrije Universiteit Medical Center, De Boelelaan 1117, 1081 HV Amsterdam, The Netherlands. Phone: 31-20-4444052. Fax: 31-20-4442964. E-mail: j.middeldorp{at}vumc.nl

{triangledown} Published ahead of print on 25 March 2009.

Clinical and Vaccine Immunology, May 2009, p. 706-711, Vol. 16, No. 5
1071-412X/09/$08.00+0     doi:10.1128/CVI.00425-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.





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