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The T-Cell Immune Response against Kaposi's Sarcoma-Associated Herpesvirus

Kaposi's sarcoma-associated herpesvirus (KSHV) is the aetiological agent of Kaposi's sarcoma (KS), the most frequently arising malignancy in individuals with untreated HIV/AIDS. There are several lines of evidence to indicate that Kaposi's sarcoma oncogenesis is associated with loss o...

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Detalles Bibliográficos
Autores principales: Robey, Rebecca C., Mletzko, Salvinia, Gotch, Frances M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275983/
https://www.ncbi.nlm.nih.gov/pubmed/22331985
http://dx.doi.org/10.1155/2010/340356
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author Robey, Rebecca C.
Mletzko, Salvinia
Gotch, Frances M.
author_facet Robey, Rebecca C.
Mletzko, Salvinia
Gotch, Frances M.
author_sort Robey, Rebecca C.
collection PubMed
description Kaposi's sarcoma-associated herpesvirus (KSHV) is the aetiological agent of Kaposi's sarcoma (KS), the most frequently arising malignancy in individuals with untreated HIV/AIDS. There are several lines of evidence to indicate that Kaposi's sarcoma oncogenesis is associated with loss of T-cell-mediated control of KSHV-infected cells. KSHV can establish life-long asymptomatic infection in immune-competent individuals. However, when T-cell immune control declines, for example, through AIDS or treatment with immunosuppressive drugs, both the prevalence of KSHV infection and the incidence of KS in KSHV carriers dramatically increase. Moreover, a dramatic and spontaneous improvement in KS is frequently seen when immunity is restored, for example, through antiretroviral therapy or the cessation of iatrogenic drugs. In this paper we describe the current state of knowledge on the T-cell immune responses against KSHV.
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spelling pubmed-32759832012-02-13 The T-Cell Immune Response against Kaposi's Sarcoma-Associated Herpesvirus Robey, Rebecca C. Mletzko, Salvinia Gotch, Frances M. Adv Virol Review Article Kaposi's sarcoma-associated herpesvirus (KSHV) is the aetiological agent of Kaposi's sarcoma (KS), the most frequently arising malignancy in individuals with untreated HIV/AIDS. There are several lines of evidence to indicate that Kaposi's sarcoma oncogenesis is associated with loss of T-cell-mediated control of KSHV-infected cells. KSHV can establish life-long asymptomatic infection in immune-competent individuals. However, when T-cell immune control declines, for example, through AIDS or treatment with immunosuppressive drugs, both the prevalence of KSHV infection and the incidence of KS in KSHV carriers dramatically increase. Moreover, a dramatic and spontaneous improvement in KS is frequently seen when immunity is restored, for example, through antiretroviral therapy or the cessation of iatrogenic drugs. In this paper we describe the current state of knowledge on the T-cell immune responses against KSHV. Hindawi Publishing Corporation 2010 2011-01-16 /pmc/articles/PMC3275983/ /pubmed/22331985 http://dx.doi.org/10.1155/2010/340356 Text en Copyright © 2010 Rebecca C. Robey et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Robey, Rebecca C.
Mletzko, Salvinia
Gotch, Frances M.
The T-Cell Immune Response against Kaposi's Sarcoma-Associated Herpesvirus
title The T-Cell Immune Response against Kaposi's Sarcoma-Associated Herpesvirus
title_full The T-Cell Immune Response against Kaposi's Sarcoma-Associated Herpesvirus
title_fullStr The T-Cell Immune Response against Kaposi's Sarcoma-Associated Herpesvirus
title_full_unstemmed The T-Cell Immune Response against Kaposi's Sarcoma-Associated Herpesvirus
title_short The T-Cell Immune Response against Kaposi's Sarcoma-Associated Herpesvirus
title_sort t-cell immune response against kaposi's sarcoma-associated herpesvirus
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275983/
https://www.ncbi.nlm.nih.gov/pubmed/22331985
http://dx.doi.org/10.1155/2010/340356
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