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CMV Immunoglobulins for the Treatment of CMV Infections in Thoracic Transplant Recipients

Intravenous ganciclovir and, increasingly, oral valganciclovir are now considered the mainstay of treatment for cytomegalovirus (CMV) infection or CMV disease. Under certain circumstances, CMV immunoglobulin (CMVIG) may be an appropriate addition or, indeed, alternative. Data on monotherapy with CMV...

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Autores principales: Schulz, Uwe, Solidoro, Paolo, Müller, Veronika, Szabo, Attila, Gottlieb, Jens, Wilkens, Heinrike, Enseleit, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764017/
https://www.ncbi.nlm.nih.gov/pubmed/26900992
http://dx.doi.org/10.1097/TP.0000000000001097
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author Schulz, Uwe
Solidoro, Paolo
Müller, Veronika
Szabo, Attila
Gottlieb, Jens
Wilkens, Heinrike
Enseleit, Frank
author_facet Schulz, Uwe
Solidoro, Paolo
Müller, Veronika
Szabo, Attila
Gottlieb, Jens
Wilkens, Heinrike
Enseleit, Frank
author_sort Schulz, Uwe
collection PubMed
description Intravenous ganciclovir and, increasingly, oral valganciclovir are now considered the mainstay of treatment for cytomegalovirus (CMV) infection or CMV disease. Under certain circumstances, CMV immunoglobulin (CMVIG) may be an appropriate addition or, indeed, alternative. Data on monotherapy with CMVIG are limited, but encouraging, for example in cases of ganciclovir intolerance. In cases of recurrent CMV in thoracic transplant patients after a disease- and drug-free period, adjunctive CMVIG can be considered in patients with hypogammaglobulinemia. Antiviral-resistant CMV, which is more common among thoracic organ recipients than in other types of transplant, can be an indication for introduction of CMVIG, particularly in view of the toxicity associated with other options, such as foscarnet. Due to a lack of controlled trials, decision-making is based on clinical experience. In the absence of a robust evidence base, it seems reasonable to consider the use of CMVIG to treat CMV in adult or pediatric thoracic transplant patients with ganciclovir-resistant infection, or in serious or complicated cases. The latter can potentially include (i) treatment of severe clinical manifestations, such as pneumonitis or eye complications; (ii) patients with a positive biopsy in end organs, such as the lung or stomach; (iii) symptomatic cases with rising polymerase chain reaction values (for example, higher than 5.0 log(10)) despite antiviral treatment; (iv) CMV disease or CMV infection or risk factors, such as CMV-IgG–negative serostatus; (vi) ganciclovir intolerance; (vii) patients with hypogammaglobulinemia.
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spelling pubmed-47640172016-03-01 CMV Immunoglobulins for the Treatment of CMV Infections in Thoracic Transplant Recipients Schulz, Uwe Solidoro, Paolo Müller, Veronika Szabo, Attila Gottlieb, Jens Wilkens, Heinrike Enseleit, Frank Transplantation Supplement Intravenous ganciclovir and, increasingly, oral valganciclovir are now considered the mainstay of treatment for cytomegalovirus (CMV) infection or CMV disease. Under certain circumstances, CMV immunoglobulin (CMVIG) may be an appropriate addition or, indeed, alternative. Data on monotherapy with CMVIG are limited, but encouraging, for example in cases of ganciclovir intolerance. In cases of recurrent CMV in thoracic transplant patients after a disease- and drug-free period, adjunctive CMVIG can be considered in patients with hypogammaglobulinemia. Antiviral-resistant CMV, which is more common among thoracic organ recipients than in other types of transplant, can be an indication for introduction of CMVIG, particularly in view of the toxicity associated with other options, such as foscarnet. Due to a lack of controlled trials, decision-making is based on clinical experience. In the absence of a robust evidence base, it seems reasonable to consider the use of CMVIG to treat CMV in adult or pediatric thoracic transplant patients with ganciclovir-resistant infection, or in serious or complicated cases. The latter can potentially include (i) treatment of severe clinical manifestations, such as pneumonitis or eye complications; (ii) patients with a positive biopsy in end organs, such as the lung or stomach; (iii) symptomatic cases with rising polymerase chain reaction values (for example, higher than 5.0 log(10)) despite antiviral treatment; (iv) CMV disease or CMV infection or risk factors, such as CMV-IgG–negative serostatus; (vi) ganciclovir intolerance; (vii) patients with hypogammaglobulinemia. Lippincott Williams & Wilkins 2016-03 2016-02-22 /pmc/articles/PMC4764017/ /pubmed/26900992 http://dx.doi.org/10.1097/TP.0000000000001097 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially.
spellingShingle Supplement
Schulz, Uwe
Solidoro, Paolo
Müller, Veronika
Szabo, Attila
Gottlieb, Jens
Wilkens, Heinrike
Enseleit, Frank
CMV Immunoglobulins for the Treatment of CMV Infections in Thoracic Transplant Recipients
title CMV Immunoglobulins for the Treatment of CMV Infections in Thoracic Transplant Recipients
title_full CMV Immunoglobulins for the Treatment of CMV Infections in Thoracic Transplant Recipients
title_fullStr CMV Immunoglobulins for the Treatment of CMV Infections in Thoracic Transplant Recipients
title_full_unstemmed CMV Immunoglobulins for the Treatment of CMV Infections in Thoracic Transplant Recipients
title_short CMV Immunoglobulins for the Treatment of CMV Infections in Thoracic Transplant Recipients
title_sort cmv immunoglobulins for the treatment of cmv infections in thoracic transplant recipients
topic Supplement
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764017/
https://www.ncbi.nlm.nih.gov/pubmed/26900992
http://dx.doi.org/10.1097/TP.0000000000001097
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