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Assessment of interleukin-17A, C5a and RANTES for early diagnosis of neonatal sepsis – a preliminary study
The aim of the present study was to investigate serum levels of novel markers: interleukin 17A (IL-17A), anaphylatoxin C5a and chemokine regulated upon activation normal T-cell expressed and secreted (RANTES) in neonates with clinically suspected early-onset neonatal sepsis (EONS), and to compare th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Polish Society of Experimental and Clinical Immunology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382877/ https://www.ncbi.nlm.nih.gov/pubmed/28450800 http://dx.doi.org/10.5114/ceji.2016.64783 |
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author | Kasztelewicz, Beata Piotrowska, Ewa Tołłoczko, Justyna Borszewska-Kornacka, Maria K. Gregorek, Hanna Dzierżanowska-Fangrat, Katarzyna |
author_facet | Kasztelewicz, Beata Piotrowska, Ewa Tołłoczko, Justyna Borszewska-Kornacka, Maria K. Gregorek, Hanna Dzierżanowska-Fangrat, Katarzyna |
author_sort | Kasztelewicz, Beata |
collection | PubMed |
description | The aim of the present study was to investigate serum levels of novel markers: interleukin 17A (IL-17A), anaphylatoxin C5a and chemokine regulated upon activation normal T-cell expressed and secreted (RANTES) in neonates with clinically suspected early-onset neonatal sepsis (EONS), and to compare their values with those of non-infected neonates. Eighteen neonates with clinical signs and symptoms of EONS were enrolled in this study. Fifty healthy, non-infected neonates served as the control group. In all neonates serum levels of IL-17A, C5a and RANTES were measured by solid-phase sandwich enzyme-linked immunosorbent assay (ELISA). At the time of investigation serum levels of anaphylatoxin C5a were significantly higher in neonates with clinical symptoms of EONS than in non-infected neonates (median 65.35 vs. 50.4 ng/ml, p = 0.034), whereas levels of RANTES were similar and levels of IL-17A were under detection limit of the method. Based on these preliminary results, serum levels of C5a may be a useful marker of inflammation in early onset neonatal sepsis. Because traditional methods of microbiological diagnostics in EONS are frequently unsuccessful, the search for an alternative laboratory biomarkers is of great clinical importance. Thus, there is a strong need for further studies evaluating usefulness of this anaphylatoxin in EONS diagnosis on a larger group of patients. |
format | Online Article Text |
id | pubmed-5382877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Polish Society of Experimental and Clinical Immunology |
record_format | MEDLINE/PubMed |
spelling | pubmed-53828772017-04-27 Assessment of interleukin-17A, C5a and RANTES for early diagnosis of neonatal sepsis – a preliminary study Kasztelewicz, Beata Piotrowska, Ewa Tołłoczko, Justyna Borszewska-Kornacka, Maria K. Gregorek, Hanna Dzierżanowska-Fangrat, Katarzyna Cent Eur J Immunol Clinical Immunology The aim of the present study was to investigate serum levels of novel markers: interleukin 17A (IL-17A), anaphylatoxin C5a and chemokine regulated upon activation normal T-cell expressed and secreted (RANTES) in neonates with clinically suspected early-onset neonatal sepsis (EONS), and to compare their values with those of non-infected neonates. Eighteen neonates with clinical signs and symptoms of EONS were enrolled in this study. Fifty healthy, non-infected neonates served as the control group. In all neonates serum levels of IL-17A, C5a and RANTES were measured by solid-phase sandwich enzyme-linked immunosorbent assay (ELISA). At the time of investigation serum levels of anaphylatoxin C5a were significantly higher in neonates with clinical symptoms of EONS than in non-infected neonates (median 65.35 vs. 50.4 ng/ml, p = 0.034), whereas levels of RANTES were similar and levels of IL-17A were under detection limit of the method. Based on these preliminary results, serum levels of C5a may be a useful marker of inflammation in early onset neonatal sepsis. Because traditional methods of microbiological diagnostics in EONS are frequently unsuccessful, the search for an alternative laboratory biomarkers is of great clinical importance. Thus, there is a strong need for further studies evaluating usefulness of this anaphylatoxin in EONS diagnosis on a larger group of patients. Polish Society of Experimental and Clinical Immunology 2017-01-24 2016 /pmc/articles/PMC5382877/ /pubmed/28450800 http://dx.doi.org/10.5114/ceji.2016.64783 Text en Copyright: © 2017 Polish Society of Experimental and Clinical Immunology http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Clinical Immunology Kasztelewicz, Beata Piotrowska, Ewa Tołłoczko, Justyna Borszewska-Kornacka, Maria K. Gregorek, Hanna Dzierżanowska-Fangrat, Katarzyna Assessment of interleukin-17A, C5a and RANTES for early diagnosis of neonatal sepsis – a preliminary study |
title | Assessment of interleukin-17A, C5a and RANTES for early diagnosis of neonatal sepsis – a preliminary study |
title_full | Assessment of interleukin-17A, C5a and RANTES for early diagnosis of neonatal sepsis – a preliminary study |
title_fullStr | Assessment of interleukin-17A, C5a and RANTES for early diagnosis of neonatal sepsis – a preliminary study |
title_full_unstemmed | Assessment of interleukin-17A, C5a and RANTES for early diagnosis of neonatal sepsis – a preliminary study |
title_short | Assessment of interleukin-17A, C5a and RANTES for early diagnosis of neonatal sepsis – a preliminary study |
title_sort | assessment of interleukin-17a, c5a and rantes for early diagnosis of neonatal sepsis – a preliminary study |
topic | Clinical Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382877/ https://www.ncbi.nlm.nih.gov/pubmed/28450800 http://dx.doi.org/10.5114/ceji.2016.64783 |
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