Regulation of the Macroautophagic Machinery, Cellular Differentiation, and Immune Responses by Human Oncogenic γ-Herpesviruses

The human γ-herpesviruses Epstein-Barr virus (EBV) and Kaposi sarcoma-associated herpesvirus (KSHV) encode oncogenes for B cell transformation but are carried by most infected individuals without symptoms. For this purpose, they manipulate the anti-apoptotic pathway macroautophagy, cellular prolifer...

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Main Author: Christian Münz
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/13/5/859
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spelling doaj-53c0f44ecfbd489aba7c4570c22690652021-05-31T23:26:45ZengMDPI AGViruses1999-49152021-05-011385985910.3390/v13050859Regulation of the Macroautophagic Machinery, Cellular Differentiation, and Immune Responses by Human Oncogenic γ-HerpesvirusesChristian Münz0Laboratory of Viral Immunobiology, Institute of Experimental Immunology, University of Zürich, 8057 Zürich, SwitzerlandThe human γ-herpesviruses Epstein-Barr virus (EBV) and Kaposi sarcoma-associated herpesvirus (KSHV) encode oncogenes for B cell transformation but are carried by most infected individuals without symptoms. For this purpose, they manipulate the anti-apoptotic pathway macroautophagy, cellular proliferation and apoptosis, as well as immune recognition. The mechanisms and functional relevance of these manipulations are discussed in this review. They allow both viruses to strike the balance between efficient persistence and dissemination in their human hosts without ever being cleared after infection and avoiding pathologies in most of their carriers.https://www.mdpi.com/1999-4915/13/5/859Epstein-Barr virus (EBV)Kaposi sarcoma-associated herpesvirus (KSHV)lymphomasimmune escapeT cell responsesco-infections
collection DOAJ
language English
format Article
sources DOAJ
author Christian Münz
spellingShingle Christian Münz
Regulation of the Macroautophagic Machinery, Cellular Differentiation, and Immune Responses by Human Oncogenic γ-Herpesviruses
Viruses
Epstein-Barr virus (EBV)
Kaposi sarcoma-associated herpesvirus (KSHV)
lymphomas
immune escape
T cell responses
co-infections
author_facet Christian Münz
author_sort Christian Münz
title Regulation of the Macroautophagic Machinery, Cellular Differentiation, and Immune Responses by Human Oncogenic γ-Herpesviruses
title_short Regulation of the Macroautophagic Machinery, Cellular Differentiation, and Immune Responses by Human Oncogenic γ-Herpesviruses
title_full Regulation of the Macroautophagic Machinery, Cellular Differentiation, and Immune Responses by Human Oncogenic γ-Herpesviruses
title_fullStr Regulation of the Macroautophagic Machinery, Cellular Differentiation, and Immune Responses by Human Oncogenic γ-Herpesviruses
title_full_unstemmed Regulation of the Macroautophagic Machinery, Cellular Differentiation, and Immune Responses by Human Oncogenic γ-Herpesviruses
title_sort regulation of the macroautophagic machinery, cellular differentiation, and immune responses by human oncogenic γ-herpesviruses
publisher MDPI AG
series Viruses
issn 1999-4915
publishDate 2021-05-01
description The human γ-herpesviruses Epstein-Barr virus (EBV) and Kaposi sarcoma-associated herpesvirus (KSHV) encode oncogenes for B cell transformation but are carried by most infected individuals without symptoms. For this purpose, they manipulate the anti-apoptotic pathway macroautophagy, cellular proliferation and apoptosis, as well as immune recognition. The mechanisms and functional relevance of these manipulations are discussed in this review. They allow both viruses to strike the balance between efficient persistence and dissemination in their human hosts without ever being cleared after infection and avoiding pathologies in most of their carriers.
topic Epstein-Barr virus (EBV)
Kaposi sarcoma-associated herpesvirus (KSHV)
lymphomas
immune escape
T cell responses
co-infections
url https://www.mdpi.com/1999-4915/13/5/859
work_keys_str_mv AT christianmunz regulationofthemacroautophagicmachinerycellulardifferentiationandimmuneresponsesbyhumanoncogenicgherpesviruses
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