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Cerebrospinal fluid chemokine patterns in children with enterovirus 71-related encephalitis
Enterovirus 71 (EV71) is a major pathogen that causes hand, foot and mouth disease (HFMD) as well as neurological complications, such as encephalitis. The chemokines involved in the migration of leukocytes have increasingly been implicated in infectious diseases of the central nervous system. Few st...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786096/ https://www.ncbi.nlm.nih.gov/pubmed/29374213 http://dx.doi.org/10.1038/s41598-018-19988-6 |
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author | Liu, Jinling Li, Shuxian Cai, Chunyan Xu, Yingchun Jiang, Yuan Chen, Zhimin |
author_facet | Liu, Jinling Li, Shuxian Cai, Chunyan Xu, Yingchun Jiang, Yuan Chen, Zhimin |
author_sort | Liu, Jinling |
collection | PubMed |
description | Enterovirus 71 (EV71) is a major pathogen that causes hand, foot and mouth disease (HFMD) as well as neurological complications, such as encephalitis. The chemokines involved in the migration of leukocytes have increasingly been implicated in infectious diseases of the central nervous system. Few studies have evaluated the levels of chemokines in HMFD children with EV71-related encephalitis. In the present study, we evaluated the cerebrospinal fluid (CSF) levels of the chemokines IL-8, RANTES, MIG, MCP-1 and IP-10 in 99 children with EV71-related encephalitis and 22 children with febrile convulsion (FC). We found that the concentrations of IL-8, RANTES, MIG and IP-10 were significantly higher in HFMD children with encephalitis compared to patients with FC. Additionally, these four chemokines were dramatically reduced during convalescence. Inversely, the level of MCP-1 was lower in encephalitis patients than FC patients and was not significantly reduced during convalescence. Additionally, MIG was strongly correlated with IP-10 in encephalitis patients. Furthermore, the area under the ROC curve (AUC) of CSF MIG and IP-10 in distinguishing encephalitis from FC were 0.869 and 0.876, and the corresponding sensitivities/specificities were 67.7%/100.0% and 67.7%/95.5%, respectively. In conclusion, our results indicate that chemokines play important roles in the pathogenesis of EV71 infection. |
format | Online Article Text |
id | pubmed-5786096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57860962018-02-07 Cerebrospinal fluid chemokine patterns in children with enterovirus 71-related encephalitis Liu, Jinling Li, Shuxian Cai, Chunyan Xu, Yingchun Jiang, Yuan Chen, Zhimin Sci Rep Article Enterovirus 71 (EV71) is a major pathogen that causes hand, foot and mouth disease (HFMD) as well as neurological complications, such as encephalitis. The chemokines involved in the migration of leukocytes have increasingly been implicated in infectious diseases of the central nervous system. Few studies have evaluated the levels of chemokines in HMFD children with EV71-related encephalitis. In the present study, we evaluated the cerebrospinal fluid (CSF) levels of the chemokines IL-8, RANTES, MIG, MCP-1 and IP-10 in 99 children with EV71-related encephalitis and 22 children with febrile convulsion (FC). We found that the concentrations of IL-8, RANTES, MIG and IP-10 were significantly higher in HFMD children with encephalitis compared to patients with FC. Additionally, these four chemokines were dramatically reduced during convalescence. Inversely, the level of MCP-1 was lower in encephalitis patients than FC patients and was not significantly reduced during convalescence. Additionally, MIG was strongly correlated with IP-10 in encephalitis patients. Furthermore, the area under the ROC curve (AUC) of CSF MIG and IP-10 in distinguishing encephalitis from FC were 0.869 and 0.876, and the corresponding sensitivities/specificities were 67.7%/100.0% and 67.7%/95.5%, respectively. In conclusion, our results indicate that chemokines play important roles in the pathogenesis of EV71 infection. Nature Publishing Group UK 2018-01-26 /pmc/articles/PMC5786096/ /pubmed/29374213 http://dx.doi.org/10.1038/s41598-018-19988-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Liu, Jinling Li, Shuxian Cai, Chunyan Xu, Yingchun Jiang, Yuan Chen, Zhimin Cerebrospinal fluid chemokine patterns in children with enterovirus 71-related encephalitis |
title | Cerebrospinal fluid chemokine patterns in children with enterovirus 71-related encephalitis |
title_full | Cerebrospinal fluid chemokine patterns in children with enterovirus 71-related encephalitis |
title_fullStr | Cerebrospinal fluid chemokine patterns in children with enterovirus 71-related encephalitis |
title_full_unstemmed | Cerebrospinal fluid chemokine patterns in children with enterovirus 71-related encephalitis |
title_short | Cerebrospinal fluid chemokine patterns in children with enterovirus 71-related encephalitis |
title_sort | cerebrospinal fluid chemokine patterns in children with enterovirus 71-related encephalitis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786096/ https://www.ncbi.nlm.nih.gov/pubmed/29374213 http://dx.doi.org/10.1038/s41598-018-19988-6 |
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