A modified IgG avidity assay for reliability improvement of an in-house capture ELISA to discriminate primary from secondary dengue virus infections

Author:

Palabodeewat Somnuek,Masrinoul Promsin,Yoksan Sutee,Auewarakul Prasert,Komaikul JukrapunORCID

Funder

Center for Vaccine Development, Institute of Molecular Biosciences, Mahidol University, Thailand

Publisher

Elsevier BV

Subject

Virology

Reference19 articles.

1. Detection of low-avidity immunoglobulin G in oral fluid samples: new approach for rubella diagnosis and surveillance;Akingbade;Clin. Diagn. Lab. Immunol.,2003

2. IgM capture ELISA for detection of IgM antibodies to dengue virus: comparison of 2 formats using hemagglutinins and cell culture derived antigens;Cardosa;Southeast Asian J. Trop. Med. Public Health,1992

3. Evaluation of the diagnostic accuracy of a new dengue IgA capture assay (Platelia Dengue IgA Capture, Bio-Rad) for dengue infection detection;De Decker;PLoS Negl. Trop. Dis.,2015

4. Use of an immunoglobulin G avidity test to discriminate between primary and secondary dengue virus infections;De Souza;J. Clin. Microbiol.,2004

5. Molecular and serologic markers of acute dengue infection in naive and flavivirus-vaccinated travelers;Domingo;Diagn. Microbiol. Infect. Dis.,2009

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3. A Critical Analysis of Intracranial Hemorrhage as a Fatal Complication of Dengue Fever;Journal of Korean Neurosurgical Society;2023-09-01

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