2007
DOI: 10.1016/j.jcv.2007.04.003
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Evaluation of immunoglobulin M and G capture enzyme-linked immunosorbent assay Panbio kits for diagnostic dengue infections

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Cited by 52 publications
(41 citation statements)
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References 37 publications
(37 reference statements)
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“…However, this is likely a minor effect because the prevalence of IgM antibodies against dengue was similar among patients who came to a hospital within the first four days of symptom onset (9.4%) compared with patients who came to a hospital within 5-10 days of symptom onset (9.7%). Moreover, the sensitivity of the assay was high, ranging from 83.5% to 96.8%, as reported in several studies, [55][56][57][58] irrespective of the sample collection period from the onset of illness.…”
Section: 54mentioning
confidence: 66%
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“…However, this is likely a minor effect because the prevalence of IgM antibodies against dengue was similar among patients who came to a hospital within the first four days of symptom onset (9.4%) compared with patients who came to a hospital within 5-10 days of symptom onset (9.7%). Moreover, the sensitivity of the assay was high, ranging from 83.5% to 96.8%, as reported in several studies, [55][56][57][58] irrespective of the sample collection period from the onset of illness.…”
Section: 54mentioning
confidence: 66%
“…However, the high specificity (99%) of the PanBio (Windsor, Queensland, Australia) IgM ELISA reported in several studies suggests that few of our cases were misclassified. 56,57,60 In Bangladesh, dengue is a year-round threat in urban and rural areas. As vaccine trials continue, 61, 62 a community-based dengue vaccination campaign could be piloted and evaluated as a possible prevention strategy.…”
Section: 54mentioning
confidence: 99%
“…Although a positive anti-DENV IgM result in the setting of an acute febrile illness is often considered diagnostic of acute DENV infection, this approach can be problematic because anti-DENV IgM is often detectable for 2-3 months after initial infection. 41 Moreover, the reported sensitivity and specificity of the DENV serologic assays used in this study have varied widely against conventional standard tests [42][43][44][45] and little is known about the performance of any DENV serologic assay in East Africa. Consequently, positive anti-DENV serology has obvious shortcomings for confirming acute symptomatic DENV infection in our study.…”
Section: Discussionmentioning
confidence: 99%
“…Because all serum samples were collected early after fever onset (between 0 and 5 days), a sample was defined as primary infection when negative for IgG and as secondary infection when positive for IgG. 24,25 The presence of NS1 was qualitatively determined using the Platelia™ NS1 Ag enzyme immunoassay (Bio-Rad Laboratories, Marnes-la-Coquette, France) as indicated by the manufacturer. For quantification of NS1 levels in serum samples with the same assay, standard curves were constructed by using two-fold serial dilutions of affinity-purified recombinant NS1 from DENV-2 expressed in Escherichia coli (kindly provided by Dr. Ronaldo Mohana-Borges, Univesidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil).…”
Section: Introductionmentioning
confidence: 99%