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Epstein–Barr virus-positive T/NK-cell lymphoproliferative disorders
Epstein–Barr virus, a ubiquitous human herpesvirus, can induce both lytic and latent infections that result in a variety of human diseases, including lymphoproliferative disorders. The oncogenic potential of Epstein–Barr virus is related to its ability to infect and transform B lymphocytes into cont...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314580/ https://www.ncbi.nlm.nih.gov/pubmed/25613730 http://dx.doi.org/10.1038/emm.2014.105 |
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author | Cai, Qingqing Chen, Kailin Young, Ken H |
author_facet | Cai, Qingqing Chen, Kailin Young, Ken H |
author_sort | Cai, Qingqing |
collection | PubMed |
description | Epstein–Barr virus, a ubiquitous human herpesvirus, can induce both lytic and latent infections that result in a variety of human diseases, including lymphoproliferative disorders. The oncogenic potential of Epstein–Barr virus is related to its ability to infect and transform B lymphocytes into continuously proliferating lymphoblastoid cells. However, Epstein–Barr virus has also been implicated in the development of T/natural killer cell lymphoproliferative diseases. Epstein–Barr virus encodes a series of products that mimic several growth, transcription and anti-apoptotic factors, thus usurping control of pathways that regulate diverse homeostatic cellular functions and the microenvironment. However, the exact mechanism by which Epstein–Barr virus promotes oncogenesis and inflammatory lesion development remains unclear. Epstein–Barr virus-associated T/natural killer cell lymphoproliferative diseases often have overlapping clinical symptoms as well as histologic and immunophenotypic features because both lymphoid cell types derive from a common precursor. Accurate classification of Epstein–Barr virus-associated T/natural killer cell lymphoproliferative diseases is a prerequisite for appropriate clinical management. Currently, the treatment of most T/natural killer cell lymphoproliferative diseases is less than satisfactory. Novel and targeted therapies are strongly required to satisfy clinical demands. This review describes our current knowledge of the genetics, oncogenesis, biology, diagnosis and treatment of Epstein–Barr virus-associated T/natural killer cell lymphoproliferative diseases. |
format | Online Article Text |
id | pubmed-4314580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43145802015-02-11 Epstein–Barr virus-positive T/NK-cell lymphoproliferative disorders Cai, Qingqing Chen, Kailin Young, Ken H Exp Mol Med Review Epstein–Barr virus, a ubiquitous human herpesvirus, can induce both lytic and latent infections that result in a variety of human diseases, including lymphoproliferative disorders. The oncogenic potential of Epstein–Barr virus is related to its ability to infect and transform B lymphocytes into continuously proliferating lymphoblastoid cells. However, Epstein–Barr virus has also been implicated in the development of T/natural killer cell lymphoproliferative diseases. Epstein–Barr virus encodes a series of products that mimic several growth, transcription and anti-apoptotic factors, thus usurping control of pathways that regulate diverse homeostatic cellular functions and the microenvironment. However, the exact mechanism by which Epstein–Barr virus promotes oncogenesis and inflammatory lesion development remains unclear. Epstein–Barr virus-associated T/natural killer cell lymphoproliferative diseases often have overlapping clinical symptoms as well as histologic and immunophenotypic features because both lymphoid cell types derive from a common precursor. Accurate classification of Epstein–Barr virus-associated T/natural killer cell lymphoproliferative diseases is a prerequisite for appropriate clinical management. Currently, the treatment of most T/natural killer cell lymphoproliferative diseases is less than satisfactory. Novel and targeted therapies are strongly required to satisfy clinical demands. This review describes our current knowledge of the genetics, oncogenesis, biology, diagnosis and treatment of Epstein–Barr virus-associated T/natural killer cell lymphoproliferative diseases. Nature Publishing Group 2015-01 2015-01-23 /pmc/articles/PMC4314580/ /pubmed/25613730 http://dx.doi.org/10.1038/emm.2014.105 Text en Copyright © 2015 KSBMB. http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported 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-nc-nd/3.0/ |
spellingShingle | Review Cai, Qingqing Chen, Kailin Young, Ken H Epstein–Barr virus-positive T/NK-cell lymphoproliferative disorders |
title | Epstein–Barr virus-positive T/NK-cell lymphoproliferative disorders |
title_full | Epstein–Barr virus-positive T/NK-cell lymphoproliferative disorders |
title_fullStr | Epstein–Barr virus-positive T/NK-cell lymphoproliferative disorders |
title_full_unstemmed | Epstein–Barr virus-positive T/NK-cell lymphoproliferative disorders |
title_short | Epstein–Barr virus-positive T/NK-cell lymphoproliferative disorders |
title_sort | epstein–barr virus-positive t/nk-cell lymphoproliferative disorders |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314580/ https://www.ncbi.nlm.nih.gov/pubmed/25613730 http://dx.doi.org/10.1038/emm.2014.105 |
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