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Open AccessJournal ArticleDOI

Multisite Monoclonal Immunoassay for Dengue Viruses: Detection of Viraemic Human Sera and Interference by Heterologous Antibody

TLDR
The antigen capture RIA appears useful as a rapid diagnostic technique for dengue surveillance and was more frequently detected in cases of primary infection than in Cases of superinfection.
Abstract
A monoclonal radioimmunoassay (RIA) was developed for detection of dengue virus in infected cell culture fluids and blood samples from dengue patients. Antibodies used to construct the RIA were selected on the basis of high binding avidity, the demonstration of synergism in competitive binding assays and empirical trials with different antibody combinations. Optimal binding of all four dengue virus serotypes was achieved by use of a flavivirus group-reactive and a dengue virus complex-reactive antibody as radiolabelled probe. A 'simultaneous sandwich' format and prolonged (18 h) incubation at 37 degrees C yielded optimal results. The limit of sensitivity of the RIA for detection of dengue type 2 virus was 2.7 log10 mosquito 50% infectious doses (MID50). The assay was tenfold more sensitive for dengue type 2 than for dengue types 1 and 3 viruses and 100-fold more sensitive than for dengue type 4 virus. Specificity, assessed using over 500 disease control human sera, was increased by addition of monoclonal anti-tetanus blocking antibodies, resulting in a false positive rate of only 0.2%. Heterologous dengue virus antibodies were shown to inhibit the RIA in assays performed with artificial immune complexes. Acute phase human sera containing 10(4.2) to 10(7.6) MID50 but no detectable antigen by RIA, were also shown to inhibit binding of the homologous dengue virus serotype; this effect was attributed to heterologous antibody from a prior infection. Among 116 viraemic sera from dengue patients, the RIA was positive in 43 to 47% of patients with dengue type 1, 2 or 3 infections but in only 10% of the dengue type 4 cases. Virus was more frequently detected in cases of primary infection (54%) than in cases of superinfection (16%). Despite the limitations imposed by immunological interference, the antigen capture RIA appears useful as a rapid diagnostic technique for dengue surveillance.

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Citations
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Journal ArticleDOI

The dengue viruses.

TL;DR: Patients present with a severe febrile illness characterized by abnormalities of hemostasis and increased vascular permeability, which in some instances results in a hypovolemic shock.
Journal ArticleDOI

An Antigen Capture Enzyme-Linked Immunosorbent Assay Reveals High Levels of the Dengue Virus Protein NS1 in the Sera of Infected Patients

TL;DR: The presence of high levels of secreted NS1 in the sera of patients experiencing secondary d Dengue virus infections, and in the context of an anamnestic antibody response, suggests that NS1 may contribute significantly to the formation of the circulating immune complexes that are suspected to play an important role in the pathogenesis of severe dengue disease.
Journal ArticleDOI

Dengue diagnosis, advances and challenges

TL;DR: An appropriate rapid, early and accessible diagnostic method useful both for epidemiological surveillance and clinical diagnosis is still needed, and laboratory infrastructure, technical expertise and research capacity must be improved in endemic countries in order to positively influence dengue surveillance.
Journal ArticleDOI

Monoclonal antibody mapping of the envelope glycoprotein of the dengue 2 virus, Jamaica

TL;DR: A set of murine monoclonal antibodies specific for the envelope (E) glycoprotein of DEN 2 virus is prepared and used in a comprehensive biological and biochemical analysis to identify 16 epitopes, which elicited potent neutralizers of virus infectivity and blocked hemagglutination, but did not block virus-mediated cell-membrane fusion.
Book ChapterDOI

Antigenic structure of flavivirus proteins.

TL;DR: This chapter reviews current understanding of the antigenic fine structure of flaviviral structural and nonstructural (NS) proteins and their involvement in B- an T-cell host responses.
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Journal ArticleDOI

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