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Diagnosing tick-borne encephalitis: a re-evaluation of notified cases

We set out to investigate the serological response of TBE virus (TBEV)-specific IgM and IgG antibodies in stored serum and cerebrospinal fluid (CSF) in notified TBE patients, in order to confirm or reject the diagnosis. We applied the ELISA methods used in clinical practice, Enzygnost and Immunozym,...

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Autores principales: Veje, Malin, Studahl, Marie, Johansson, Maja, Johansson, Patrik, Nolskog, Peter, Bergström, Tomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780526/
https://www.ncbi.nlm.nih.gov/pubmed/29188467
http://dx.doi.org/10.1007/s10096-017-3139-9
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author Veje, Malin
Studahl, Marie
Johansson, Maja
Johansson, Patrik
Nolskog, Peter
Bergström, Tomas
author_facet Veje, Malin
Studahl, Marie
Johansson, Maja
Johansson, Patrik
Nolskog, Peter
Bergström, Tomas
author_sort Veje, Malin
collection PubMed
description We set out to investigate the serological response of TBE virus (TBEV)-specific IgM and IgG antibodies in stored serum and cerebrospinal fluid (CSF) in notified TBE patients, in order to confirm or reject the diagnosis. We applied the ELISA methods used in clinical practice, Enzygnost and Immunozym, and assessed RT-PCR as a diagnostic tool. A total of 173 TBE cases were notified to the Public Health Agency. Samples from 129 patients were eligible for the study. Stored serum samples were found for 111 patients and CSF samples for 88 patients. All serum samples were analyzed with both Enzygnost and Immunozym, as well as an additional 140 control samples. CSF samples, including samples from ten controls, were analyzed with Immunozym. RT-PCR for TBEV was performed on 126 serum, two whole blood, 96 CSF, two feces and four nasopharynx samples. Only two of 111 notified patients lacked detectable TBEV IgM in serum, from whom one sample was RT-PCR positive. According to the ECDC definition, 117/129 (90.7%) of the reported TBE cases were confirmed. Positive RT-PCR results were obtained in eight patients, one from whole blood and eight from serum samples. Four out of eight of the RT-PCR positive patients were TBEV-IgM positive and none had detectable TBEV-specific IgG. All of the tested CSF, feces and nasopharynx samples were RT-PCR-negative. TBEV-specific IgG was detected in 88.4% and IgM in 31.6% of the CSF samples. RT-PCR on serum samples and CSF IgG antibodies can be used as complementary methods in TBE diagnostics, not least early in the disease course. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10096-017-3139-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-57805262018-02-01 Diagnosing tick-borne encephalitis: a re-evaluation of notified cases Veje, Malin Studahl, Marie Johansson, Maja Johansson, Patrik Nolskog, Peter Bergström, Tomas Eur J Clin Microbiol Infect Dis Original Article We set out to investigate the serological response of TBE virus (TBEV)-specific IgM and IgG antibodies in stored serum and cerebrospinal fluid (CSF) in notified TBE patients, in order to confirm or reject the diagnosis. We applied the ELISA methods used in clinical practice, Enzygnost and Immunozym, and assessed RT-PCR as a diagnostic tool. A total of 173 TBE cases were notified to the Public Health Agency. Samples from 129 patients were eligible for the study. Stored serum samples were found for 111 patients and CSF samples for 88 patients. All serum samples were analyzed with both Enzygnost and Immunozym, as well as an additional 140 control samples. CSF samples, including samples from ten controls, were analyzed with Immunozym. RT-PCR for TBEV was performed on 126 serum, two whole blood, 96 CSF, two feces and four nasopharynx samples. Only two of 111 notified patients lacked detectable TBEV IgM in serum, from whom one sample was RT-PCR positive. According to the ECDC definition, 117/129 (90.7%) of the reported TBE cases were confirmed. Positive RT-PCR results were obtained in eight patients, one from whole blood and eight from serum samples. Four out of eight of the RT-PCR positive patients were TBEV-IgM positive and none had detectable TBEV-specific IgG. All of the tested CSF, feces and nasopharynx samples were RT-PCR-negative. TBEV-specific IgG was detected in 88.4% and IgM in 31.6% of the CSF samples. RT-PCR on serum samples and CSF IgG antibodies can be used as complementary methods in TBE diagnostics, not least early in the disease course. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10096-017-3139-9) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-11-29 2018 /pmc/articles/PMC5780526/ /pubmed/29188467 http://dx.doi.org/10.1007/s10096-017-3139-9 Text en © The Author(s) 2017 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
Veje, Malin
Studahl, Marie
Johansson, Maja
Johansson, Patrik
Nolskog, Peter
Bergström, Tomas
Diagnosing tick-borne encephalitis: a re-evaluation of notified cases
title Diagnosing tick-borne encephalitis: a re-evaluation of notified cases
title_full Diagnosing tick-borne encephalitis: a re-evaluation of notified cases
title_fullStr Diagnosing tick-borne encephalitis: a re-evaluation of notified cases
title_full_unstemmed Diagnosing tick-borne encephalitis: a re-evaluation of notified cases
title_short Diagnosing tick-borne encephalitis: a re-evaluation of notified cases
title_sort diagnosing tick-borne encephalitis: a re-evaluation of notified cases
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780526/
https://www.ncbi.nlm.nih.gov/pubmed/29188467
http://dx.doi.org/10.1007/s10096-017-3139-9
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