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Epstein–Barr Virus

Epstein–Barr virus (EBV) is a ubiquitous gamma herpesvirus aetiologically linked to different lymphoid and epithelial malignancies and a number of systemic autoimmune diseases. The virus has a unique ability to transform resting B lymphocytes in vitro by expressing a set of latent genes, subsets of...

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Main Author: Mhairi Morris
Format: Default Article
Published: 2017
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Online Access:https://hdl.handle.net/2134/27474
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author Mhairi Morris
author_facet Mhairi Morris
author_sort Mhairi Morris (3718882)
collection Figshare
description Epstein–Barr virus (EBV) is a ubiquitous gamma herpesvirus aetiologically linked to different lymphoid and epithelial malignancies and a number of systemic autoimmune diseases. The virus has a unique ability to transform resting B lymphocytes in vitro by expressing a set of latent genes, subsets of which are present in EBV‐associated tumours. EBV exploits the physiology of normal B‐cell differentiation to persist within the memory B‐cell pool of the immunocompetent host with strong T‐cell responses important for controlling EBV infection. Immunosuppressed transplant recipients and human immunodeficiency virus (HIV)‐infected individuals are at increased risk of developing EBV‐transformed B‐cell proliferations which often present as monoclonal non‐Hodgkin lymphomas. The major EBV‐associated tumours (Burkitt lymphoma, Hodgkin lymphoma and nasopharyngeal carcinoma) show restricted forms of latent viral gene expression reflecting a more complex pathogenesis involving additional cofactors. A number of pharmacological and immunotherapeutic approaches are being developed to treat or prevent these EBV‐associated tumours.
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spelling rr-article-96272452017-06-22T00:00:00Z Epstein–Barr Virus Mhairi Morris (3718882) Other health sciences not elsewhere classified untagged Medical and Health Sciences not elsewhere classified Epstein–Barr virus (EBV) is a ubiquitous gamma herpesvirus aetiologically linked to different lymphoid and epithelial malignancies and a number of systemic autoimmune diseases. The virus has a unique ability to transform resting B lymphocytes in vitro by expressing a set of latent genes, subsets of which are present in EBV‐associated tumours. EBV exploits the physiology of normal B‐cell differentiation to persist within the memory B‐cell pool of the immunocompetent host with strong T‐cell responses important for controlling EBV infection. Immunosuppressed transplant recipients and human immunodeficiency virus (HIV)‐infected individuals are at increased risk of developing EBV‐transformed B‐cell proliferations which often present as monoclonal non‐Hodgkin lymphomas. The major EBV‐associated tumours (Burkitt lymphoma, Hodgkin lymphoma and nasopharyngeal carcinoma) show restricted forms of latent viral gene expression reflecting a more complex pathogenesis involving additional cofactors. A number of pharmacological and immunotherapeutic approaches are being developed to treat or prevent these EBV‐associated tumours. 2017-06-22T00:00:00Z Text Journal contribution 2134/27474 https://figshare.com/articles/journal_contribution/Epstein_Barr_Virus/9627245 CC BY-NC-ND 4.0
spellingShingle Other health sciences not elsewhere classified
untagged
Medical and Health Sciences not elsewhere classified
Mhairi Morris
Epstein–Barr Virus
title Epstein–Barr Virus
title_full Epstein–Barr Virus
title_fullStr Epstein–Barr Virus
title_full_unstemmed Epstein–Barr Virus
title_short Epstein–Barr Virus
title_sort epstein–barr virus
topic Other health sciences not elsewhere classified
untagged
Medical and Health Sciences not elsewhere classified
url https://hdl.handle.net/2134/27474