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Immunotherapy for Epstein-Barr Virus-Related Lymphomas

Latent EBV infection is associated with several malignancies, including EBV post-transplant lymphoproliferative disorders (LPD), Hodgkin and non-Hodgkin lymphomas, nasopharyngeal carcinoma and Burkitt lymphoma. The range of expression of latent EBV antigens varies in these tumors, which influences h...

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Autores principales: Kennedy-Nasser, Alana A., Bollard, Catherine M., Heslop, Helen E.
Formato: Texto
Lenguaje:English
Publicado: Università Cattolica del Sacro Cuore 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033176/
https://www.ncbi.nlm.nih.gov/pubmed/21416001
http://dx.doi.org/10.4084/MJHID.2009.010
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author Kennedy-Nasser, Alana A.
Bollard, Catherine M.
Heslop, Helen E.
author_facet Kennedy-Nasser, Alana A.
Bollard, Catherine M.
Heslop, Helen E.
author_sort Kennedy-Nasser, Alana A.
collection PubMed
description Latent EBV infection is associated with several malignancies, including EBV post-transplant lymphoproliferative disorders (LPD), Hodgkin and non-Hodgkin lymphomas, nasopharyngeal carcinoma and Burkitt lymphoma. The range of expression of latent EBV antigens varies in these tumors, which influences how susceptible the tumors are to immunotherapeutic approaches. Tumors expressing type III latency, such as in LPD, express the widest array of EBV antigens making them the most susceptible to immunotherapy. Treatment strategies for EBV-related tumors include restoring normal cellular immunity by adoptive immunotherapy with EBV-specific T cells and targeting the malignant B cells with monoclonal antibodies. We review the current immunotherapies and future studies aimed at targeting EBV antigen expression in these tumors.
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spelling pubmed-30331762011-03-17 Immunotherapy for Epstein-Barr Virus-Related Lymphomas Kennedy-Nasser, Alana A. Bollard, Catherine M. Heslop, Helen E. Mediterr J Hematol Infect Dis Review Article Latent EBV infection is associated with several malignancies, including EBV post-transplant lymphoproliferative disorders (LPD), Hodgkin and non-Hodgkin lymphomas, nasopharyngeal carcinoma and Burkitt lymphoma. The range of expression of latent EBV antigens varies in these tumors, which influences how susceptible the tumors are to immunotherapeutic approaches. Tumors expressing type III latency, such as in LPD, express the widest array of EBV antigens making them the most susceptible to immunotherapy. Treatment strategies for EBV-related tumors include restoring normal cellular immunity by adoptive immunotherapy with EBV-specific T cells and targeting the malignant B cells with monoclonal antibodies. We review the current immunotherapies and future studies aimed at targeting EBV antigen expression in these tumors. Università Cattolica del Sacro Cuore 2009-11-17 /pmc/articles/PMC3033176/ /pubmed/21416001 http://dx.doi.org/10.4084/MJHID.2009.010 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Kennedy-Nasser, Alana A.
Bollard, Catherine M.
Heslop, Helen E.
Immunotherapy for Epstein-Barr Virus-Related Lymphomas
title Immunotherapy for Epstein-Barr Virus-Related Lymphomas
title_full Immunotherapy for Epstein-Barr Virus-Related Lymphomas
title_fullStr Immunotherapy for Epstein-Barr Virus-Related Lymphomas
title_full_unstemmed Immunotherapy for Epstein-Barr Virus-Related Lymphomas
title_short Immunotherapy for Epstein-Barr Virus-Related Lymphomas
title_sort immunotherapy for epstein-barr virus-related lymphomas
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033176/
https://www.ncbi.nlm.nih.gov/pubmed/21416001
http://dx.doi.org/10.4084/MJHID.2009.010
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