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The Novel Immunosuppressive Protein Kinase C Inhibitor Sotrastaurin Has No Pro-Viral Effects on the Replication Cycle of Hepatitis B or C Virus

The pan-protein kinase C (PKC) inhibitor sotrastaurin (AEB071) is a novel immunosuppressant currently in phase II trials for immunosuppression after solid organ transplantation. Besides T-cell activation, PKC affects numerous cellular processes that are potentially important for the replication of h...

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Autores principales: von Hahn, Thomas, Schulze, Andreas, Chicano Wust, Ivan, Heidrich, Benjamin, Becker, Thomas, Steinmann, Eike, Helfritz, Fabian A., Rohrmann, Katrin, Urban, Stephan, Manns, Michael P., Pietschmann, Thomas, Ciesek, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164709/
https://www.ncbi.nlm.nih.gov/pubmed/21909416
http://dx.doi.org/10.1371/journal.pone.0024142
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author von Hahn, Thomas
Schulze, Andreas
Chicano Wust, Ivan
Heidrich, Benjamin
Becker, Thomas
Steinmann, Eike
Helfritz, Fabian A.
Rohrmann, Katrin
Urban, Stephan
Manns, Michael P.
Pietschmann, Thomas
Ciesek, Sandra
author_facet von Hahn, Thomas
Schulze, Andreas
Chicano Wust, Ivan
Heidrich, Benjamin
Becker, Thomas
Steinmann, Eike
Helfritz, Fabian A.
Rohrmann, Katrin
Urban, Stephan
Manns, Michael P.
Pietschmann, Thomas
Ciesek, Sandra
author_sort von Hahn, Thomas
collection PubMed
description The pan-protein kinase C (PKC) inhibitor sotrastaurin (AEB071) is a novel immunosuppressant currently in phase II trials for immunosuppression after solid organ transplantation. Besides T-cell activation, PKC affects numerous cellular processes that are potentially important for the replication of hepatitis B virus (HBV) and hepatitis C virus (HCV), major blood-borne pathogens prevalent in solid organ transplant recipients. This study uses state of the art virological assays to assess the direct, non-immune mediated effects of sotrastaurin on HBV and HCV. Most importantly, sotrastaurin had no pro-viral effect on either HBV or HCV. In the presence of high concentrations of sotrastaurin, well above those used clinically and close to levels where cytotoxic effects become detectable, there was a reduction of HCV and HBV replication. This reduction is very likely due to cytotoxic and/or anti-proliferative effects rather than direct anti-viral activity of the drug. Replication cycle stages other than genome replication such as viral cell entry and spread of HCV infection directly between adjacent cells was clearly unaffected by sotrastaurin. These data support the evaluation of sotrastaurin in HBV and/or HCV infected transplant recipients.
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spelling pubmed-31647092011-09-09 The Novel Immunosuppressive Protein Kinase C Inhibitor Sotrastaurin Has No Pro-Viral Effects on the Replication Cycle of Hepatitis B or C Virus von Hahn, Thomas Schulze, Andreas Chicano Wust, Ivan Heidrich, Benjamin Becker, Thomas Steinmann, Eike Helfritz, Fabian A. Rohrmann, Katrin Urban, Stephan Manns, Michael P. Pietschmann, Thomas Ciesek, Sandra PLoS One Research Article The pan-protein kinase C (PKC) inhibitor sotrastaurin (AEB071) is a novel immunosuppressant currently in phase II trials for immunosuppression after solid organ transplantation. Besides T-cell activation, PKC affects numerous cellular processes that are potentially important for the replication of hepatitis B virus (HBV) and hepatitis C virus (HCV), major blood-borne pathogens prevalent in solid organ transplant recipients. This study uses state of the art virological assays to assess the direct, non-immune mediated effects of sotrastaurin on HBV and HCV. Most importantly, sotrastaurin had no pro-viral effect on either HBV or HCV. In the presence of high concentrations of sotrastaurin, well above those used clinically and close to levels where cytotoxic effects become detectable, there was a reduction of HCV and HBV replication. This reduction is very likely due to cytotoxic and/or anti-proliferative effects rather than direct anti-viral activity of the drug. Replication cycle stages other than genome replication such as viral cell entry and spread of HCV infection directly between adjacent cells was clearly unaffected by sotrastaurin. These data support the evaluation of sotrastaurin in HBV and/or HCV infected transplant recipients. Public Library of Science 2011-09-01 /pmc/articles/PMC3164709/ /pubmed/21909416 http://dx.doi.org/10.1371/journal.pone.0024142 Text en von Hahn et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
von Hahn, Thomas
Schulze, Andreas
Chicano Wust, Ivan
Heidrich, Benjamin
Becker, Thomas
Steinmann, Eike
Helfritz, Fabian A.
Rohrmann, Katrin
Urban, Stephan
Manns, Michael P.
Pietschmann, Thomas
Ciesek, Sandra
The Novel Immunosuppressive Protein Kinase C Inhibitor Sotrastaurin Has No Pro-Viral Effects on the Replication Cycle of Hepatitis B or C Virus
title The Novel Immunosuppressive Protein Kinase C Inhibitor Sotrastaurin Has No Pro-Viral Effects on the Replication Cycle of Hepatitis B or C Virus
title_full The Novel Immunosuppressive Protein Kinase C Inhibitor Sotrastaurin Has No Pro-Viral Effects on the Replication Cycle of Hepatitis B or C Virus
title_fullStr The Novel Immunosuppressive Protein Kinase C Inhibitor Sotrastaurin Has No Pro-Viral Effects on the Replication Cycle of Hepatitis B or C Virus
title_full_unstemmed The Novel Immunosuppressive Protein Kinase C Inhibitor Sotrastaurin Has No Pro-Viral Effects on the Replication Cycle of Hepatitis B or C Virus
title_short The Novel Immunosuppressive Protein Kinase C Inhibitor Sotrastaurin Has No Pro-Viral Effects on the Replication Cycle of Hepatitis B or C Virus
title_sort novel immunosuppressive protein kinase c inhibitor sotrastaurin has no pro-viral effects on the replication cycle of hepatitis b or c virus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164709/
https://www.ncbi.nlm.nih.gov/pubmed/21909416
http://dx.doi.org/10.1371/journal.pone.0024142
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