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Monoclonal antibody-based capture ELISA in the diagnosis of previous dengue infection

BACKGROUND: Dengue is an important mosquito-borne disease. There is currently only one licensed vaccine for dengue prevention. The vaccine provides higher efficacy in pre-vaccination dengue-seropositive persons but a higher risk of subsequent more severe dengue in dengue-seronegative persons. It is...

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Autores principales: Sirivichayakul, Chukiat, Limkittikul, Kriengsak, Chanthavanich, Pornthep, Yoksan, Sutee, Ratchatatat, Anuttarasakdi, Lim, Jacqueline Kyungah, Arunsodsai, Watcharee, Sabchareon, Arunee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820907/
https://www.ncbi.nlm.nih.gov/pubmed/31665014
http://dx.doi.org/10.1186/s12985-019-1222-9
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author Sirivichayakul, Chukiat
Limkittikul, Kriengsak
Chanthavanich, Pornthep
Yoksan, Sutee
Ratchatatat, Anuttarasakdi
Lim, Jacqueline Kyungah
Arunsodsai, Watcharee
Sabchareon, Arunee
author_facet Sirivichayakul, Chukiat
Limkittikul, Kriengsak
Chanthavanich, Pornthep
Yoksan, Sutee
Ratchatatat, Anuttarasakdi
Lim, Jacqueline Kyungah
Arunsodsai, Watcharee
Sabchareon, Arunee
author_sort Sirivichayakul, Chukiat
collection PubMed
description BACKGROUND: Dengue is an important mosquito-borne disease. There is currently only one licensed vaccine for dengue prevention. The vaccine provides higher efficacy in pre-vaccination dengue-seropositive persons but a higher risk of subsequent more severe dengue in dengue-seronegative persons. It is recommended that the dengue vaccine may be given in dengue-seropositive individuals or as mass vaccination without individual pre-vaccination screening in areas where the dengue seroprevalence is > 80% in children aged 9 years. We evaluated a dengue specific immunoglobulin G monoclonal antibody-based capture enzyme-linked immunosorbent assay (MAb-ELISA) in the diagnosis of previous dengue infection using serum samples from the cohort study in Ratchaburi Province, Thailand. METHODS: The MAb-ELISA was compared to 70% plaque reduction neutralization test (PRNT70) in 453 serum samples from children aged 3–11 years in Ratchaburi Province, Thailand. RESULTS: The sensitivity and specificity of MAb-ELISA at the positive to negative (P/N) ratio cut-off level of > 3 were both 0.91 in the diagnosis of previous dengue infection, compared to PRNT70. The false positivity was mainly in Japanese encephalitis (JE) seropositive subjects. CONCLUSIONS: This research provides evidence that MAb-ELISA is useful for dengue seroprevalence study and dengue pre-vaccination screening. JE seropositivity was the major cause of false positive result in the study population.
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spelling pubmed-68209072019-11-04 Monoclonal antibody-based capture ELISA in the diagnosis of previous dengue infection Sirivichayakul, Chukiat Limkittikul, Kriengsak Chanthavanich, Pornthep Yoksan, Sutee Ratchatatat, Anuttarasakdi Lim, Jacqueline Kyungah Arunsodsai, Watcharee Sabchareon, Arunee Virol J Research BACKGROUND: Dengue is an important mosquito-borne disease. There is currently only one licensed vaccine for dengue prevention. The vaccine provides higher efficacy in pre-vaccination dengue-seropositive persons but a higher risk of subsequent more severe dengue in dengue-seronegative persons. It is recommended that the dengue vaccine may be given in dengue-seropositive individuals or as mass vaccination without individual pre-vaccination screening in areas where the dengue seroprevalence is > 80% in children aged 9 years. We evaluated a dengue specific immunoglobulin G monoclonal antibody-based capture enzyme-linked immunosorbent assay (MAb-ELISA) in the diagnosis of previous dengue infection using serum samples from the cohort study in Ratchaburi Province, Thailand. METHODS: The MAb-ELISA was compared to 70% plaque reduction neutralization test (PRNT70) in 453 serum samples from children aged 3–11 years in Ratchaburi Province, Thailand. RESULTS: The sensitivity and specificity of MAb-ELISA at the positive to negative (P/N) ratio cut-off level of > 3 were both 0.91 in the diagnosis of previous dengue infection, compared to PRNT70. The false positivity was mainly in Japanese encephalitis (JE) seropositive subjects. CONCLUSIONS: This research provides evidence that MAb-ELISA is useful for dengue seroprevalence study and dengue pre-vaccination screening. JE seropositivity was the major cause of false positive result in the study population. BioMed Central 2019-10-29 /pmc/articles/PMC6820907/ /pubmed/31665014 http://dx.doi.org/10.1186/s12985-019-1222-9 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Sirivichayakul, Chukiat
Limkittikul, Kriengsak
Chanthavanich, Pornthep
Yoksan, Sutee
Ratchatatat, Anuttarasakdi
Lim, Jacqueline Kyungah
Arunsodsai, Watcharee
Sabchareon, Arunee
Monoclonal antibody-based capture ELISA in the diagnosis of previous dengue infection
title Monoclonal antibody-based capture ELISA in the diagnosis of previous dengue infection
title_full Monoclonal antibody-based capture ELISA in the diagnosis of previous dengue infection
title_fullStr Monoclonal antibody-based capture ELISA in the diagnosis of previous dengue infection
title_full_unstemmed Monoclonal antibody-based capture ELISA in the diagnosis of previous dengue infection
title_short Monoclonal antibody-based capture ELISA in the diagnosis of previous dengue infection
title_sort monoclonal antibody-based capture elisa in the diagnosis of previous dengue infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820907/
https://www.ncbi.nlm.nih.gov/pubmed/31665014
http://dx.doi.org/10.1186/s12985-019-1222-9
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