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Evaluation of Eosinophilic Cationic Protein as a Marker of Alveolar and Cystic Echinococcosis

Echinococcosis is a neglected zoonotic disease and a worldwide public health problem caused by infection with the larval stages of taeniid cestodes of the genus Echinococcus. In vitro studies have demonstrated a protoscolecidal effect of eosinophilic cationic protein (ECP), a granule protein of eosi...

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Autores principales: Hotz, Julian Frederic, Kaczirek, Klaus, Stremitzer, Stefan, Waneck, Fredrik, Auer, Herbert, Perkmann, Thomas, Kussmann, Manuel, Bauer, Philipp Karl, Chen, Rui-Yang, Kriz, Richard, Burgmann, Heinz, Ramharter, Michael, Lagler, Heimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878807/
https://www.ncbi.nlm.nih.gov/pubmed/35215203
http://dx.doi.org/10.3390/pathogens11020261
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author Hotz, Julian Frederic
Kaczirek, Klaus
Stremitzer, Stefan
Waneck, Fredrik
Auer, Herbert
Perkmann, Thomas
Kussmann, Manuel
Bauer, Philipp Karl
Chen, Rui-Yang
Kriz, Richard
Burgmann, Heinz
Ramharter, Michael
Lagler, Heimo
author_facet Hotz, Julian Frederic
Kaczirek, Klaus
Stremitzer, Stefan
Waneck, Fredrik
Auer, Herbert
Perkmann, Thomas
Kussmann, Manuel
Bauer, Philipp Karl
Chen, Rui-Yang
Kriz, Richard
Burgmann, Heinz
Ramharter, Michael
Lagler, Heimo
author_sort Hotz, Julian Frederic
collection PubMed
description Echinococcosis is a neglected zoonotic disease and a worldwide public health problem caused by infection with the larval stages of taeniid cestodes of the genus Echinococcus. In vitro studies have demonstrated a protoscolecidal effect of eosinophilic cationic protein (ECP), a granule protein of eosinophilic granulocytes, against E. granulosus. Therefore, the main objective of this study was to evaluate ECP as a biomarker in the treatment of alveolar echinococcosis (AE) and cystic echinococcosis (CE). Data were collected retrospectively from the Vienna Echinococcosis Cohort over 7 years until December 2020. Altogether, 32 patients (16 AE and 16 CE) were included. In the selected patients, serum ECP values were compared before and after the beginning of an operative and/or benzimidazole (BMZ) therapy. Mean ECP serum levels before intervention were significantly (p < 0.05) elevated at 34.0 ± 22.9 μg/L in AE patients and at 38.6 ± 19.9 μg/L in CE patients compared to the control group. After the intervention, mean ECP levels decreased significantly (p < 0.05) to 20.4 ± 14.6 μg/L in AE patients and to 22.4 ± 8.3 μg/L in CE patients. Furthermore, ECP showed a significant (p < 0.05) correlation of k = 0.56 with PET–CTI. Based on the significant decrease after operative and/or BMZ treatment and the correlation with clinical markers such as PET–CTI, it is recommended to investigate ECP more intensively as a marker of AE and CE in prospective studies with larger cohorts.
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spelling pubmed-88788072022-02-26 Evaluation of Eosinophilic Cationic Protein as a Marker of Alveolar and Cystic Echinococcosis Hotz, Julian Frederic Kaczirek, Klaus Stremitzer, Stefan Waneck, Fredrik Auer, Herbert Perkmann, Thomas Kussmann, Manuel Bauer, Philipp Karl Chen, Rui-Yang Kriz, Richard Burgmann, Heinz Ramharter, Michael Lagler, Heimo Pathogens Article Echinococcosis is a neglected zoonotic disease and a worldwide public health problem caused by infection with the larval stages of taeniid cestodes of the genus Echinococcus. In vitro studies have demonstrated a protoscolecidal effect of eosinophilic cationic protein (ECP), a granule protein of eosinophilic granulocytes, against E. granulosus. Therefore, the main objective of this study was to evaluate ECP as a biomarker in the treatment of alveolar echinococcosis (AE) and cystic echinococcosis (CE). Data were collected retrospectively from the Vienna Echinococcosis Cohort over 7 years until December 2020. Altogether, 32 patients (16 AE and 16 CE) were included. In the selected patients, serum ECP values were compared before and after the beginning of an operative and/or benzimidazole (BMZ) therapy. Mean ECP serum levels before intervention were significantly (p < 0.05) elevated at 34.0 ± 22.9 μg/L in AE patients and at 38.6 ± 19.9 μg/L in CE patients compared to the control group. After the intervention, mean ECP levels decreased significantly (p < 0.05) to 20.4 ± 14.6 μg/L in AE patients and to 22.4 ± 8.3 μg/L in CE patients. Furthermore, ECP showed a significant (p < 0.05) correlation of k = 0.56 with PET–CTI. Based on the significant decrease after operative and/or BMZ treatment and the correlation with clinical markers such as PET–CTI, it is recommended to investigate ECP more intensively as a marker of AE and CE in prospective studies with larger cohorts. MDPI 2022-02-18 /pmc/articles/PMC8878807/ /pubmed/35215203 http://dx.doi.org/10.3390/pathogens11020261 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hotz, Julian Frederic
Kaczirek, Klaus
Stremitzer, Stefan
Waneck, Fredrik
Auer, Herbert
Perkmann, Thomas
Kussmann, Manuel
Bauer, Philipp Karl
Chen, Rui-Yang
Kriz, Richard
Burgmann, Heinz
Ramharter, Michael
Lagler, Heimo
Evaluation of Eosinophilic Cationic Protein as a Marker of Alveolar and Cystic Echinococcosis
title Evaluation of Eosinophilic Cationic Protein as a Marker of Alveolar and Cystic Echinococcosis
title_full Evaluation of Eosinophilic Cationic Protein as a Marker of Alveolar and Cystic Echinococcosis
title_fullStr Evaluation of Eosinophilic Cationic Protein as a Marker of Alveolar and Cystic Echinococcosis
title_full_unstemmed Evaluation of Eosinophilic Cationic Protein as a Marker of Alveolar and Cystic Echinococcosis
title_short Evaluation of Eosinophilic Cationic Protein as a Marker of Alveolar and Cystic Echinococcosis
title_sort evaluation of eosinophilic cationic protein as a marker of alveolar and cystic echinococcosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878807/
https://www.ncbi.nlm.nih.gov/pubmed/35215203
http://dx.doi.org/10.3390/pathogens11020261
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