Evaluation of the Panbio dengue virus nonstructural 1 antigen detection and immunoglobulin M antibody enzyme-linked immunosorbent assays for the diagnosis of acute dengue infections in Laos

Abstract We evaluated 2 commercial enzyme-linked immunosorbent assays (ELISAs) for the diagnosis of dengue infection; one a serologic test for immunoglobulin M (IgM) antibodies, the other based on detection of dengue virus nonstructural 1 (NS1) antigen. Using gold standard reference serology on pair...

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Published in:Diagnostic microbiology and infectious disease Vol. 60; no. 1; pp. 43 - 49
Main Authors: Blacksell, Stuart D, Mammen, Mammen P, Thongpaseuth, Soulignasack, Gibbons, Robert V, Jarman, Richard G, Jenjaroen, Kemajittra, Nisalak, Ananda, Phetsouvanh, Rattanaphone, Newton, Paul N, Day, Nicholas P.J
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Language:English
Published: New York, NY Elsevier Inc 2008
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Abstract Abstract We evaluated 2 commercial enzyme-linked immunosorbent assays (ELISAs) for the diagnosis of dengue infection; one a serologic test for immunoglobulin M (IgM) antibodies, the other based on detection of dengue virus nonstructural 1 (NS1) antigen. Using gold standard reference serology on paired sera, 41% (38/92 patients) were dengue confirmed, with 4 (11%) acute primary and 33 (87%) acute secondary infections (1 was of indeterminate status). Sensitivity of the NS1-ELISA was 63% (95% confidence interval [CI], 53–73) on admission samples but was much less sensitive (5%; 95% CI, 1–10) on convalescent samples. The IgM capture ELISA had a lower but statistically equivalent sensitivity compared with the NS1-ELISA for admission samples (45%; 95% CI, 35–55) but was more sensitive on convalescent samples (58%; 95% CI, 48–68). The results of the NS1 and IgM capture ELISAs were combined using a logical OR operator, increasing the sensitivity for admission samples (79%; 95% CI, 71–87), convalescent samples (63%; 95% CI, 53–73), and all samples (71%; 95% CI, 65–78).
AbstractList We evaluated 2 commercial enzyme-linked immunosorbent assays (ELISAs) for the diagnosis of dengue infection; one a serologic test for immunoglobulin M (IgM) antibodies, the other based on detection of dengue virus nonstructural 1 (NS1) antigen. Using gold standard reference serology on paired sera, 41% (38/92 patients) were dengue confirmed, with 4 (11%) acute primary and 33 (87%) acute secondary infections (1 was of indeterminate status). Sensitivity of the NS1-ELISA was 63% (95% confidence interval [CI], 53–73) on admission samples but was much less sensitive (5%; 95% CI, 1–10) on convalescent samples. The IgM capture ELISA had a lower but statistically equivalent sensitivity compared with the NS1-ELISA for admission samples (45%; 95% CI, 35–55) but was more sensitive on convalescent samples (58%; 95% CI, 48–68). The results of the NS1 and IgM capture ELISAs were combined using a logical OR operator, increasing the sensitivity for admission samples (79%; 95% CI, 71–87), convalescent samples (63%; 95% CI, 53–73), and all samples (71%; 95% CI, 65–78).
Abstract We evaluated 2 commercial enzyme-linked immunosorbent assays (ELISAs) for the diagnosis of dengue infection; one a serologic test for immunoglobulin M (IgM) antibodies, the other based on detection of dengue virus nonstructural 1 (NS1) antigen. Using gold standard reference serology on paired sera, 41% (38/92 patients) were dengue confirmed, with 4 (11%) acute primary and 33 (87%) acute secondary infections (1 was of indeterminate status). Sensitivity of the NS1-ELISA was 63% (95% confidence interval [CI], 53–73) on admission samples but was much less sensitive (5%; 95% CI, 1–10) on convalescent samples. The IgM capture ELISA had a lower but statistically equivalent sensitivity compared with the NS1-ELISA for admission samples (45%; 95% CI, 35–55) but was more sensitive on convalescent samples (58%; 95% CI, 48–68). The results of the NS1 and IgM capture ELISAs were combined using a logical OR operator, increasing the sensitivity for admission samples (79%; 95% CI, 71–87), convalescent samples (63%; 95% CI, 53–73), and all samples (71%; 95% CI, 65–78).
Author Blacksell, Stuart D
Nisalak, Ananda
Day, Nicholas P.J
Mammen, Mammen P
Jarman, Richard G
Gibbons, Robert V
Newton, Paul N
Thongpaseuth, Soulignasack
Phetsouvanh, Rattanaphone
Jenjaroen, Kemajittra
Author_xml – sequence: 1
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  fullname: Mammen, Mammen P
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  fullname: Thongpaseuth, Soulignasack
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  fullname: Gibbons, Robert V
– sequence: 5
  fullname: Jarman, Richard G
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  fullname: Jenjaroen, Kemajittra
– sequence: 7
  fullname: Nisalak, Ananda
– sequence: 8
  fullname: Phetsouvanh, Rattanaphone
– sequence: 9
  fullname: Newton, Paul N
– sequence: 10
  fullname: Day, Nicholas P.J
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Issue 1
Keywords Dengue
Immunochromatographic
Serology
Diagnosis
Point-of-care
Laos
NS1
IgM
Antibody
Acute
Dengue virus 1
Flavivirus
Infection
Virus
Antigen
Viral disease
Dengue group virus
Arbovirus disease
Flaviviridae
Detection
ELISA assay
Language English
License CC BY 4.0
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Snippet Abstract We evaluated 2 commercial enzyme-linked immunosorbent assays (ELISAs) for the diagnosis of dengue infection; one a serologic test for immunoglobulin M...
We evaluated 2 commercial enzyme-linked immunosorbent assays (ELISAs) for the diagnosis of dengue infection; one a serologic test for immunoglobulin M (IgM)...
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SubjectTerms Antibodies, Viral - blood
Antigens, Viral - blood
Arboviroses
Biological and medical sciences
Dengue
Dengue - diagnosis
Dengue fevers
Dengue virus
Dengue Virus - immunology
Dengue Virus - isolation & purification
Diagnosis
Enzyme-Linked Immunosorbent Assay - methods
Fundamental and applied biological sciences. Psychology
Human viral diseases
Humans
IgM
Immunochromatographic
Immunoglobulin M - blood
Infectious Disease
Infectious diseases
Internal Medicine
Laos
Medical sciences
Microbiology
Miscellaneous
NS1
Point-of-care
Sensitivity and Specificity
Serology
Tropical viral diseases
Viral diseases
Viral Nonstructural Proteins - blood
Virology
Title Evaluation of the Panbio dengue virus nonstructural 1 antigen detection and immunoglobulin M antibody enzyme-linked immunosorbent assays for the diagnosis of acute dengue infections in Laos
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https://www.ncbi.nlm.nih.gov/pubmed/17889487
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