Abstract
A lung and kidney transplant recipient underwent cytomegalovirus (CMV) primary infection with a UL97 mutation. Combined monitoring of viral load and CMV-specific CD4 T-cells allowed reduction of treatment duration with foscarnet, and illustrates how knowledge on the individual immunocompetence towards CMV may be used to individualize duration of antiviral treatment.
Keywords:
Antiviral therapy; Cytomegalovirus; Resistance; Solid organ transplantation; T-cell.
Copyright © 2016 Elsevier B.V. All rights reserved.
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Antiviral Agents / administration & dosage*
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Antiviral Agents / pharmacology
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CD4-Positive T-Lymphocytes / immunology
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Cytomegalovirus / drug effects*
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Cytomegalovirus Infections / drug therapy*
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Cytomegalovirus Infections / virology
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Drug Monitoring / methods*
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Drug Resistance, Viral*
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Female
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Foscarnet / administration & dosage*
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Ganciclovir / pharmacology
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Humans
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Kidney Transplantation
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Lung Transplantation
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Transplant Recipients
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Viral Load
Substances
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Antiviral Agents
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Foscarnet
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Ganciclovir