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Herpesviruses in the Activated Phosphatidylinositol-3-Kinase-δ Syndrome
The phosphatidylinositol-3-kinase (PI3K)/Akt pathway is important for multiple stages of herpesvirus replication including virus entry, replication, latency, and reactivation. Recently, patients with gain-of-function mutations in the p110δ-catalytic subunit of PI3K or in the p85-regulatory subunit o...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863522/ https://www.ncbi.nlm.nih.gov/pubmed/29599765 http://dx.doi.org/10.3389/fimmu.2018.00237 |
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author | Cohen, Jeffrey I. |
author_facet | Cohen, Jeffrey I. |
author_sort | Cohen, Jeffrey I. |
collection | PubMed |
description | The phosphatidylinositol-3-kinase (PI3K)/Akt pathway is important for multiple stages of herpesvirus replication including virus entry, replication, latency, and reactivation. Recently, patients with gain-of-function mutations in the p110δ-catalytic subunit of PI3K or in the p85-regulatory subunit of PI3K have been reported. These patients have constitutively active PI3K with hyperactivation of Akt. They present with lymphoproliferation and often have infections, particularly recurrent respiratory infections and/or severe virus infections. The most frequent virus infections are due to Epstein–Barr virus (EBV) and cytomegalovirus (CMV); patients often present with persistent EBV and/or CMV viremia, EBV lymphoproliferative disease, or CMV lymphadenitis. No patients have been reported with CMV pneumonia, colitis, or retinitis. Other herpesvirus infections have included herpes simplex pneumonia, recurrent zoster, and varicella after vaccination with the varicella vaccine. Additional viral infections have included adenovirus viremia, severe warts, and extensive Molluscum contagiosum virus infection. The increased susceptibility to virus infections in these patients is likely due to a reduced number of long-lived memory CD8 T cells and an increased number of terminally differentiated effector CD8 T cells. |
format | Online Article Text |
id | pubmed-5863522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58635222018-03-29 Herpesviruses in the Activated Phosphatidylinositol-3-Kinase-δ Syndrome Cohen, Jeffrey I. Front Immunol Immunology The phosphatidylinositol-3-kinase (PI3K)/Akt pathway is important for multiple stages of herpesvirus replication including virus entry, replication, latency, and reactivation. Recently, patients with gain-of-function mutations in the p110δ-catalytic subunit of PI3K or in the p85-regulatory subunit of PI3K have been reported. These patients have constitutively active PI3K with hyperactivation of Akt. They present with lymphoproliferation and often have infections, particularly recurrent respiratory infections and/or severe virus infections. The most frequent virus infections are due to Epstein–Barr virus (EBV) and cytomegalovirus (CMV); patients often present with persistent EBV and/or CMV viremia, EBV lymphoproliferative disease, or CMV lymphadenitis. No patients have been reported with CMV pneumonia, colitis, or retinitis. Other herpesvirus infections have included herpes simplex pneumonia, recurrent zoster, and varicella after vaccination with the varicella vaccine. Additional viral infections have included adenovirus viremia, severe warts, and extensive Molluscum contagiosum virus infection. The increased susceptibility to virus infections in these patients is likely due to a reduced number of long-lived memory CD8 T cells and an increased number of terminally differentiated effector CD8 T cells. Frontiers Media S.A. 2018-02-23 /pmc/articles/PMC5863522/ /pubmed/29599765 http://dx.doi.org/10.3389/fimmu.2018.00237 Text en Copyright © 2018 This work is authored by Jeffrey I. Cohen on behalf of the U.S. Government and, as regards Dr. Cohen and the US government, is not subject to copyright protection in the United States. Foreign and other copyrights may apply. 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 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 Cohen, Jeffrey I. Herpesviruses in the Activated Phosphatidylinositol-3-Kinase-δ Syndrome |
title | Herpesviruses in the Activated Phosphatidylinositol-3-Kinase-δ Syndrome |
title_full | Herpesviruses in the Activated Phosphatidylinositol-3-Kinase-δ Syndrome |
title_fullStr | Herpesviruses in the Activated Phosphatidylinositol-3-Kinase-δ Syndrome |
title_full_unstemmed | Herpesviruses in the Activated Phosphatidylinositol-3-Kinase-δ Syndrome |
title_short | Herpesviruses in the Activated Phosphatidylinositol-3-Kinase-δ Syndrome |
title_sort | herpesviruses in the activated phosphatidylinositol-3-kinase-δ syndrome |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863522/ https://www.ncbi.nlm.nih.gov/pubmed/29599765 http://dx.doi.org/10.3389/fimmu.2018.00237 |
work_keys_str_mv | AT cohenjeffreyi herpesvirusesintheactivatedphosphatidylinositol3kinasedsyndrome |