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KSHV: Immune Modulation and Immunotherapy

Kaposi's sarcoma (KS)-associated herpesvirus (KSHV) is associated with KS, primary effusion lymphoma (PEL), and multicentric Castleman disease (MCD). To ensure its own survival and propagation, KSHV employs an extensive network of viral proteins to subvert the host immune system, resulting in l...

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Detalles Bibliográficos
Autores principales: Broussard, Grant, Damania, Blossom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025529/
https://www.ncbi.nlm.nih.gov/pubmed/32117196
http://dx.doi.org/10.3389/fimmu.2019.03084
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author Broussard, Grant
Damania, Blossom
author_facet Broussard, Grant
Damania, Blossom
author_sort Broussard, Grant
collection PubMed
description Kaposi's sarcoma (KS)-associated herpesvirus (KSHV) is associated with KS, primary effusion lymphoma (PEL), and multicentric Castleman disease (MCD). To ensure its own survival and propagation, KSHV employs an extensive network of viral proteins to subvert the host immune system, resulting in lifelong latent infection. Modulation of cellular and systemic immune defenses allows KSHV to persist in the host, which may eventually lead to the progression of KSHV-associated cancers. Due to KSHV's reliance on modifying immune responses to efficiently infect its host, immunotherapy is an attractive option for treating KSHV-associated malignancies. In this review, we will focus on the mechanisms by which KSHV evades the immune system and the current immune-related clinical strategies to treat KSHV-associated disease.
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spelling pubmed-70255292020-02-28 KSHV: Immune Modulation and Immunotherapy Broussard, Grant Damania, Blossom Front Immunol Immunology Kaposi's sarcoma (KS)-associated herpesvirus (KSHV) is associated with KS, primary effusion lymphoma (PEL), and multicentric Castleman disease (MCD). To ensure its own survival and propagation, KSHV employs an extensive network of viral proteins to subvert the host immune system, resulting in lifelong latent infection. Modulation of cellular and systemic immune defenses allows KSHV to persist in the host, which may eventually lead to the progression of KSHV-associated cancers. Due to KSHV's reliance on modifying immune responses to efficiently infect its host, immunotherapy is an attractive option for treating KSHV-associated malignancies. In this review, we will focus on the mechanisms by which KSHV evades the immune system and the current immune-related clinical strategies to treat KSHV-associated disease. Frontiers Media S.A. 2020-02-07 /pmc/articles/PMC7025529/ /pubmed/32117196 http://dx.doi.org/10.3389/fimmu.2019.03084 Text en Copyright © 2020 Broussard and Damania. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Broussard, Grant
Damania, Blossom
KSHV: Immune Modulation and Immunotherapy
title KSHV: Immune Modulation and Immunotherapy
title_full KSHV: Immune Modulation and Immunotherapy
title_fullStr KSHV: Immune Modulation and Immunotherapy
title_full_unstemmed KSHV: Immune Modulation and Immunotherapy
title_short KSHV: Immune Modulation and Immunotherapy
title_sort kshv: immune modulation and immunotherapy
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025529/
https://www.ncbi.nlm.nih.gov/pubmed/32117196
http://dx.doi.org/10.3389/fimmu.2019.03084
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