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Development of immunochromatographic device as a point-of-care tool for serodiagnosis of human strongyloidiasis cases

Human strongyloidiasis is an important gastrointestinal disease with an estimated 30 to 100 million people infected. Prevalence is generally underestimated since many infections are asymptomatic, and traditional diagnostic tests based on parasitological examination of stool samples are not adequatel...

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Autores principales: Sadaow, Lakkhana, Sanpool, Oranuch, Rodpai, Rutchanee, Boonroumkaew, Patcharaporn, Maleewong, Wanchai, Intapan, Pewpan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7040067/
https://www.ncbi.nlm.nih.gov/pubmed/31758442
http://dx.doi.org/10.1007/s10096-019-03745-2
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author Sadaow, Lakkhana
Sanpool, Oranuch
Rodpai, Rutchanee
Boonroumkaew, Patcharaporn
Maleewong, Wanchai
Intapan, Pewpan M.
author_facet Sadaow, Lakkhana
Sanpool, Oranuch
Rodpai, Rutchanee
Boonroumkaew, Patcharaporn
Maleewong, Wanchai
Intapan, Pewpan M.
author_sort Sadaow, Lakkhana
collection PubMed
description Human strongyloidiasis is an important gastrointestinal disease with an estimated 30 to 100 million people infected. Prevalence is generally underestimated since many infections are asymptomatic, and traditional diagnostic tests based on parasitological examination of stool samples are not adequately sensitive. Serological tests are useful and supportive but are still only available in a reference research setting. We made an immunochromatographic test (ICT) kit for rapid serodiagnosis of human strongyloidiasis. The antigen used in the ICT kit was extracted from larvae of Strongyloides stercoralis. Diagnostic efficacy of the kit was evaluated using human serum samples from strongyloidiasis patients, healthy persons, and those with other parasitoses. When using a cutoff level of 0.5 or above, the diagnostic sensitivity, specificity, and positive and negative predictive values at the prevalence of infection of 34.4%, were 93.3%, 83.7%, 76.7%, and 95.6%, respectively. This ICT kit is easy to use at the point-of-care and a result can be obtained in 15 min. Sophisticated instruments and highly trained staff are not required. It can be used in several diagnostic and public-health settings, e.g., prevalence surveys in endemic areas, confirmation and monitoring of cure post-treatment, diagnosis and screening of infected but asymptomatic individuals, and populations “at risk” for hyperinfection syndrome or disseminated strongyloidiasis if they are given immunosuppressive treatment for other conditions.
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spelling pubmed-70400672020-03-10 Development of immunochromatographic device as a point-of-care tool for serodiagnosis of human strongyloidiasis cases Sadaow, Lakkhana Sanpool, Oranuch Rodpai, Rutchanee Boonroumkaew, Patcharaporn Maleewong, Wanchai Intapan, Pewpan M. Eur J Clin Microbiol Infect Dis Original Article Human strongyloidiasis is an important gastrointestinal disease with an estimated 30 to 100 million people infected. Prevalence is generally underestimated since many infections are asymptomatic, and traditional diagnostic tests based on parasitological examination of stool samples are not adequately sensitive. Serological tests are useful and supportive but are still only available in a reference research setting. We made an immunochromatographic test (ICT) kit for rapid serodiagnosis of human strongyloidiasis. The antigen used in the ICT kit was extracted from larvae of Strongyloides stercoralis. Diagnostic efficacy of the kit was evaluated using human serum samples from strongyloidiasis patients, healthy persons, and those with other parasitoses. When using a cutoff level of 0.5 or above, the diagnostic sensitivity, specificity, and positive and negative predictive values at the prevalence of infection of 34.4%, were 93.3%, 83.7%, 76.7%, and 95.6%, respectively. This ICT kit is easy to use at the point-of-care and a result can be obtained in 15 min. Sophisticated instruments and highly trained staff are not required. It can be used in several diagnostic and public-health settings, e.g., prevalence surveys in endemic areas, confirmation and monitoring of cure post-treatment, diagnosis and screening of infected but asymptomatic individuals, and populations “at risk” for hyperinfection syndrome or disseminated strongyloidiasis if they are given immunosuppressive treatment for other conditions. Springer Berlin Heidelberg 2019-11-22 2020 /pmc/articles/PMC7040067/ /pubmed/31758442 http://dx.doi.org/10.1007/s10096-019-03745-2 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Sadaow, Lakkhana
Sanpool, Oranuch
Rodpai, Rutchanee
Boonroumkaew, Patcharaporn
Maleewong, Wanchai
Intapan, Pewpan M.
Development of immunochromatographic device as a point-of-care tool for serodiagnosis of human strongyloidiasis cases
title Development of immunochromatographic device as a point-of-care tool for serodiagnosis of human strongyloidiasis cases
title_full Development of immunochromatographic device as a point-of-care tool for serodiagnosis of human strongyloidiasis cases
title_fullStr Development of immunochromatographic device as a point-of-care tool for serodiagnosis of human strongyloidiasis cases
title_full_unstemmed Development of immunochromatographic device as a point-of-care tool for serodiagnosis of human strongyloidiasis cases
title_short Development of immunochromatographic device as a point-of-care tool for serodiagnosis of human strongyloidiasis cases
title_sort development of immunochromatographic device as a point-of-care tool for serodiagnosis of human strongyloidiasis cases
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7040067/
https://www.ncbi.nlm.nih.gov/pubmed/31758442
http://dx.doi.org/10.1007/s10096-019-03745-2
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