Email updates

Keep up to date with the latest news and content from BMC Infectious Diseases and BioMed Central.

Open Access Technical advance

Enzyme-linked immunoassay for dengue virus IgM and IgG antibodies in serum and filter paper blood

Thanh Nga T Tran12, Peter J de Vries1*, Lan Phuong Hoang13, Giao T Phan13, Hung Q Le13, Binh Q Tran3, Chi Mai T Vo2, Nam V Nguyen4, Piet A Kager1, Nico Nagelkerke5 and Jan Groen67

Author Affiliations

1 Division of Infectious Diseases, Tropical Medicine and AIDS, Academic Medical Center, P.O. Box 22700, 1100 DE Amsterdam, the Netherlands Amsterdam, the Netherlands

2 Department of Microbiology, Cho Ray Hospital, 102 B Nguyen Chi Thanh, Ho Chi Minh City, Vietnam

3 Department of Tropical Diseases, Cho Ray Hospital, 102 B Nguyen Chi Thanh, Ho Chi Minh City, Vietnam

4 Binh Thuan Malaria and Goiter Control Center, 133A Hai Thuong Lan Ong, Phan Thiet, Vietnam

5 Dept of Community Medicine, United Arab Emirates University, P.O. Box 17666 Al Ain, United Arab Emirates

6 Department of Clinical Virology, Erasmus Medical Center Rotterdam, The Netherlands

7 Department of Microbiology and Virology, Focus Diagnostics, Cypress CA, USA

For all author emails, please log on.

BMC Infectious Diseases 2006, 6:13  doi:10.1186/1471-2334-6-13

Published: 25 January 2006

Abstract

Background

The reproducibilty of dengue IgM and IgG ELISA was studied in serum and filter paper blood spots from Vietnamese febrile patients.

Methods

781 pairs of acute (t0) and convalescent sera, obtained after three weeks (t3) and 161 corresponding pairs of filter paper blood spots were tested with ELISA for dengue IgG and IgM. 74 serum pairs were tested again in another laboratory with similar methods, after a mean of 252 days.

Results

Cases were classified as no dengue (10 %), past dengue (55%) acute primary (7%) or secondary (28%) dengue. Significant differences between the two laboratories' results were found leading to different diagnostic classification (kappa 0.46, p < 0.001). Filter paper results correlated poorly to serum values, being more variable and lower with a mean (95% CI) difference of 0.82 (0.36 to 1.28) for IgMt3, 0.94 (0.51 to 1.37) for IgGt0 and 0.26 (-0.20 to 0.71) for IgGt3. This also led to differences in diagnostic classification (kappa value 0.44, p < 0.001) The duration of storage of frozen serum and dried filter papers, sealed in nylon bags in an air-conditioned room, had no significant effect on the ELISA results.

Conclusion

Dengue virus IgG antibodies in serum and filter papers was not affected by duration of storage, but was subject to inter-laboratory variability. Dengue virus IgM antibodies measured in serum reconstituted from blood spots on filter papers were lower than in serum, in particular in the acute phase of disease. Therefore this method limits its value for diagnostic confirmation of individual patients with dengue virus infections.

However the detection of dengue virus IgG antibodies eluted from filter paper can be used for sero-prevalence cross sectional studies.