Early diagnosis of dengue virus infection by detection of dengue viral antigen in peripheral blood mononuclear cell

Background: An essential requirement related to treatment of dengue-infected patients is a rapid and accurate detection of dengue virus during febrile stage of the disease. OBJECTIVE: The study examined using direct immunofluorescence staining the presence of dengue viral antigen in peripheral blood...

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Main Authors: Sirichan Chunhakan, Punnee Butthep, Sutee Yoksan, Kanchana Tangnararatchakit, Ampaiwan Chuansumrit
Other Authors: Faculty of Medicine, Ramathibodi Hospital, Mahidol University
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/28241
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spelling th-mahidol.282412018-09-13T14:07:18Z Early diagnosis of dengue virus infection by detection of dengue viral antigen in peripheral blood mononuclear cell Sirichan Chunhakan Punnee Butthep Sutee Yoksan Kanchana Tangnararatchakit Ampaiwan Chuansumrit Faculty of Medicine, Ramathibodi Hospital, Mahidol University Mahidol University Medicine Background: An essential requirement related to treatment of dengue-infected patients is a rapid and accurate detection of dengue virus during febrile stage of the disease. OBJECTIVE: The study examined using direct immunofluorescence staining the presence of dengue viral antigen in peripheral blood mononuclear cells (PBMCs). Methods: Four hundred forty-five blood samples from 164 patients with dengue fever, dengue hemorrhagic fever, and other febrile illnesses were collected daily from the day of admission until discharge and also at convalescent stage. Blood smear was stained with fluorescein isothiocyanate-conjugated polyvalent dengue antiserum and examined under a fluorescent microscope. Dengue infection was confirmed by virus isolation and/or dengue-specific IgM and IgG enzyme linked immunosorbent assay test. Results: Dengue viral antigens were found in most PBMC samples of dengue infected patients collected on the day before defervescence and continued until 2 to 3 days afterward. The number of dengue viral antigen positive PBMCs was highest in patients with dengue shock syndrome. Sensitivity and specificity of this method during the febrile stage was 93.8% (95% confidence interval: 88.8%-98.9%) and 100%, respectively. The positive and negative predictive values were 100% and 69.0%, respectively. CONCLUSION: Detection of dengue viral antigen in direct PBMC smear provides a useful and rapid technique for early diagnosis of dengue virus infection. © 2009 by Lippincott Williams & Wilkins. 2018-09-13T07:07:18Z 2018-09-13T07:07:18Z 2009-01-01 Article Pediatric Infectious Disease Journal. Vol.28, No.12 (2009), 1085-1088 10.1097/INF.0b013e3181acf6a3 15320987 08913668 2-s2.0-74049124839 https://repository.li.mahidol.ac.th/handle/123456789/28241 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=74049124839&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
Sirichan Chunhakan
Punnee Butthep
Sutee Yoksan
Kanchana Tangnararatchakit
Ampaiwan Chuansumrit
Early diagnosis of dengue virus infection by detection of dengue viral antigen in peripheral blood mononuclear cell
description Background: An essential requirement related to treatment of dengue-infected patients is a rapid and accurate detection of dengue virus during febrile stage of the disease. OBJECTIVE: The study examined using direct immunofluorescence staining the presence of dengue viral antigen in peripheral blood mononuclear cells (PBMCs). Methods: Four hundred forty-five blood samples from 164 patients with dengue fever, dengue hemorrhagic fever, and other febrile illnesses were collected daily from the day of admission until discharge and also at convalescent stage. Blood smear was stained with fluorescein isothiocyanate-conjugated polyvalent dengue antiserum and examined under a fluorescent microscope. Dengue infection was confirmed by virus isolation and/or dengue-specific IgM and IgG enzyme linked immunosorbent assay test. Results: Dengue viral antigens were found in most PBMC samples of dengue infected patients collected on the day before defervescence and continued until 2 to 3 days afterward. The number of dengue viral antigen positive PBMCs was highest in patients with dengue shock syndrome. Sensitivity and specificity of this method during the febrile stage was 93.8% (95% confidence interval: 88.8%-98.9%) and 100%, respectively. The positive and negative predictive values were 100% and 69.0%, respectively. CONCLUSION: Detection of dengue viral antigen in direct PBMC smear provides a useful and rapid technique for early diagnosis of dengue virus infection. © 2009 by Lippincott Williams & Wilkins.
author2 Faculty of Medicine, Ramathibodi Hospital, Mahidol University
author_facet Faculty of Medicine, Ramathibodi Hospital, Mahidol University
Sirichan Chunhakan
Punnee Butthep
Sutee Yoksan
Kanchana Tangnararatchakit
Ampaiwan Chuansumrit
format Article
author Sirichan Chunhakan
Punnee Butthep
Sutee Yoksan
Kanchana Tangnararatchakit
Ampaiwan Chuansumrit
author_sort Sirichan Chunhakan
title Early diagnosis of dengue virus infection by detection of dengue viral antigen in peripheral blood mononuclear cell
title_short Early diagnosis of dengue virus infection by detection of dengue viral antigen in peripheral blood mononuclear cell
title_full Early diagnosis of dengue virus infection by detection of dengue viral antigen in peripheral blood mononuclear cell
title_fullStr Early diagnosis of dengue virus infection by detection of dengue viral antigen in peripheral blood mononuclear cell
title_full_unstemmed Early diagnosis of dengue virus infection by detection of dengue viral antigen in peripheral blood mononuclear cell
title_sort early diagnosis of dengue virus infection by detection of dengue viral antigen in peripheral blood mononuclear cell
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/28241
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