2012
DOI: 10.1128/cvi.05717-11
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Comparison of Seven Commercial Antigen and Antibody Enzyme-Linked Immunosorbent Assays for Detection of Acute Dengue Infection

Abstract: ABSTRACTSeven commercial assays were evaluated to determine their suitability for the diagnosis of acute dengue infection: (i) the Panbio dengue virus Pan-E NS1 early enzyme-linked immunosorbent assay (ELISA), second generation (Alere, Australia); (ii) the Panbio dengue virus IgM capture ELISA (Alere, Australia); (iii) the Panbio dengue virus IgG capture ELISA (Alere, Australia); (iv) the Standard Diagnostics dengue virus NS1 antigen ELISA (Standard Diagnostics, South Korea); (… Show more

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Cited by 115 publications
(120 citation statements)
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References 24 publications
(31 reference statements)
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“…However, an early and precise dengue diagnostic is important for patient management, to avoid dengue severity and mortality and, ultimately, to control epidemics. 8,21,26 Our results agree with others who reported that the combination of two or more diagnostic strategies is needed to improve the diagnostic accuracy of DENV infection. 8,[21][22][23]26 Combining direct DENV detection and antibody-based tests seems to be a particularly promising strategy.…”
Section: Discussionsupporting
confidence: 91%
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“…However, an early and precise dengue diagnostic is important for patient management, to avoid dengue severity and mortality and, ultimately, to control epidemics. 8,21,26 Our results agree with others who reported that the combination of two or more diagnostic strategies is needed to improve the diagnostic accuracy of DENV infection. 8,[21][22][23]26 Combining direct DENV detection and antibody-based tests seems to be a particularly promising strategy.…”
Section: Discussionsupporting
confidence: 91%
“…8,21,26 Our results agree with others who reported that the combination of two or more diagnostic strategies is needed to improve the diagnostic accuracy of DENV infection. 8,[21][22][23]26 Combining direct DENV detection and antibody-based tests seems to be a particularly promising strategy. However, as seen in this study and evidenced by the low LR+ and LR− values, combinations of current assays do not guarantee the accuracy of the diagnosis when compared with standards such as PRNT or ELISPOT-MNT.…”
Section: Discussionsupporting
confidence: 91%
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“…A cut-off value was determined and results were interpreted as positive and negative according to manufacturer's instructions [13,14] .…”
Section: Sample Processingmentioning
confidence: 99%
“…The IgA has been commented with an analogous behaviour to IgG antibody. In primary infection must be detectable after the release of IgM, while in secondary infection IgA appear early in acute phase by the common epitopes recognition by memory B cell clones circulating on blood [40] [42]. The induction of high-rate IgA levels requires a group of factors which must act synergistically in the Ig production predominantly toward IgA isotype: engagement of CD40 (B cells) by CD40 ligand (CD40L, Ag-activated CD4+ T cells) which determines class switch gene recombination; TGF-ß secreted by CD40L-induced B cells is required for switching to IgA; the presence of IL-10 increasing both the number of IgA lymphocytes and the amount of secreted IgA.…”
Section: Discussionmentioning
confidence: 99%