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Analysis of Epstein-Barr virus infection models in a series of pediatric carriers from a developing country
Epstein-Barr virus (EBV) is a B lymphotropic human herpesvirus. Two models, germinal center (GC) and direct infection, describe how EBV infects B-cells. Since in Argentina primary infection is mostly subclinical at young ages, children represent an interesting population where to analyze EBV infecti...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4796914/ https://www.ncbi.nlm.nih.gov/pubmed/26988293 http://dx.doi.org/10.1038/srep23303 |
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author | Vistarop, Aldana G. Cohen, Melina De Matteo, Elena Preciado, María Victoria Chabay, Paola A. |
author_facet | Vistarop, Aldana G. Cohen, Melina De Matteo, Elena Preciado, María Victoria Chabay, Paola A. |
author_sort | Vistarop, Aldana G. |
collection | PubMed |
description | Epstein-Barr virus (EBV) is a B lymphotropic human herpesvirus. Two models, germinal center (GC) and direct infection, describe how EBV infects B-cells. Since in Argentina primary infection is mostly subclinical at young ages, children represent an interesting population where to analyze EBV infection, especially considering that most studies are usually performed in adults. Tonsil biopsies from pediatric carriers were studied to describe infection characteristics. EBV+ lymphocytes at the interfollicular region were mainly observed. Latency III pattern in subepithelial (SubEp) lymphocytes was observed at young ages, probably indicating a recent infection. In older patients EBV was mostly detected in epithelial cells, suggesting that they could have been infected some time ago. This finding was sustained by tonsillar viral load, which was higher in cases with LMP1+SubEp cells vs. LMP1+nonSubEp cells (p = 0.0237, Mann-Whiney test). Latency III was prevalent and related to the GC, while latency II was associated with non-GC (p = 0.0159, χ2 test). EBERs+/IgD+ cells were statistically prevalent over EBERs+/CD27+ cells (p = 0.0021, χ2 test). These findings indicated that both EBV infection models are not mutually exclusive and provide some basis for further understanding of EBV infection dynamics. Moreover, we provide a more accurate explanation of EBV infection in pediatric asymptomatic carriers from a developing country. |
format | Online Article Text |
id | pubmed-4796914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47969142016-03-21 Analysis of Epstein-Barr virus infection models in a series of pediatric carriers from a developing country Vistarop, Aldana G. Cohen, Melina De Matteo, Elena Preciado, María Victoria Chabay, Paola A. Sci Rep Article Epstein-Barr virus (EBV) is a B lymphotropic human herpesvirus. Two models, germinal center (GC) and direct infection, describe how EBV infects B-cells. Since in Argentina primary infection is mostly subclinical at young ages, children represent an interesting population where to analyze EBV infection, especially considering that most studies are usually performed in adults. Tonsil biopsies from pediatric carriers were studied to describe infection characteristics. EBV+ lymphocytes at the interfollicular region were mainly observed. Latency III pattern in subepithelial (SubEp) lymphocytes was observed at young ages, probably indicating a recent infection. In older patients EBV was mostly detected in epithelial cells, suggesting that they could have been infected some time ago. This finding was sustained by tonsillar viral load, which was higher in cases with LMP1+SubEp cells vs. LMP1+nonSubEp cells (p = 0.0237, Mann-Whiney test). Latency III was prevalent and related to the GC, while latency II was associated with non-GC (p = 0.0159, χ2 test). EBERs+/IgD+ cells were statistically prevalent over EBERs+/CD27+ cells (p = 0.0021, χ2 test). These findings indicated that both EBV infection models are not mutually exclusive and provide some basis for further understanding of EBV infection dynamics. Moreover, we provide a more accurate explanation of EBV infection in pediatric asymptomatic carriers from a developing country. Nature Publishing Group 2016-03-18 /pmc/articles/PMC4796914/ /pubmed/26988293 http://dx.doi.org/10.1038/srep23303 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Vistarop, Aldana G. Cohen, Melina De Matteo, Elena Preciado, María Victoria Chabay, Paola A. Analysis of Epstein-Barr virus infection models in a series of pediatric carriers from a developing country |
title | Analysis of Epstein-Barr virus infection models in a series of pediatric carriers from a developing country |
title_full | Analysis of Epstein-Barr virus infection models in a series of pediatric carriers from a developing country |
title_fullStr | Analysis of Epstein-Barr virus infection models in a series of pediatric carriers from a developing country |
title_full_unstemmed | Analysis of Epstein-Barr virus infection models in a series of pediatric carriers from a developing country |
title_short | Analysis of Epstein-Barr virus infection models in a series of pediatric carriers from a developing country |
title_sort | analysis of epstein-barr virus infection models in a series of pediatric carriers from a developing country |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4796914/ https://www.ncbi.nlm.nih.gov/pubmed/26988293 http://dx.doi.org/10.1038/srep23303 |
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