The influence of immunosuppressive agents on BK virus risk following kidney transplantation, and implications for choice of regimen.

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The influence of immunosuppressive agents on BK virus risk following kidney transplantation, and implications for choice of regimen. / Suwelack, Barbara; Malyar, Viola; Koch, Martina; Sester, Martina; Sommerer, Claudia.

in: Transplant Rev (Orlando), Jahrgang 26, Nr. 3, 3, 2012, S. 201-211.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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Suwelack B, Malyar V, Koch M, Sester M, Sommerer C. The influence of immunosuppressive agents on BK virus risk following kidney transplantation, and implications for choice of regimen. Transplant Rev (Orlando). 2012;26(3):201-211. 3.

Bibtex

@article{dd87622904704e4badec0a6a852be985,
title = "The influence of immunosuppressive agents on BK virus risk following kidney transplantation, and implications for choice of regimen.",
abstract = "The increasing incidence of BK-associated nephropathy following kidney transplantation has prompted an examination of strategies for risk reduction and management through immunosuppression manipulation. Evidence from retrospective and prospective studies suggests that BK viruria and viremia, and the need for BK virus treatment, are higher with tacrolimus than cyclosporine. Combined therapy with tacrolimus and mycophenolic acid may be associated with a particularly higher risk of BK infection, but data are conflicting as to whether mycophenolic acid per se is an independent risk factor. The incidence of BK-related events may be reduced in patients receiving mTOR inhibitors (everolimus or sirolimus) with cyclosporine vs a calcineurin inhibitor with mycophenolic acid. De novo immunosuppression regimens that avoid rabbit antithymocyte globulin and tacrolimus, particularly tacrolimus with mycophenolic acid, may be advantageous, whereas low-exposure cyclosporine with an mTOR inhibitor appears a favorable option. Routine screening for BK infection during the first 2 years posttransplant is recommended to allow preemptive modification of the immunosuppressive regimen. In patients at high risk of BK virus infection, appropriate de novo immunosuppression or very early conversion to an mTOR inhibitor to facilitate reduction or discontinuation of calcineurin inhibitors or antimetabolites should be considered. Extensive further research into optimal avoidance, screening, and treatment strategies is required.",
keywords = "Humans, Risk Factors, TOR Serine-Threonine Kinases/antagonists & inhibitors, *Kidney Transplantation, Calcineurin/antagonists & inhibitors, Virus Replication/drug effects, Antilymphocyte Serum/pharmacology, BK Virus/*drug effects/physiology, Glucocorticoids/pharmacology, Immunosuppressive Agents/*pharmacology/therapeutic use, Mycophenolic Acid/pharmacology, Polyomavirus Infections/diagnosis/*drug therapy/etiology/virology, Tacrolimus/pharmacology, Tumor Virus Infections/diagnosis/*drug therapy/etiology/virology, Virus Activation/drug effects, Humans, Risk Factors, TOR Serine-Threonine Kinases/antagonists & inhibitors, *Kidney Transplantation, Calcineurin/antagonists & inhibitors, Virus Replication/drug effects, Antilymphocyte Serum/pharmacology, BK Virus/*drug effects/physiology, Glucocorticoids/pharmacology, Immunosuppressive Agents/*pharmacology/therapeutic use, Mycophenolic Acid/pharmacology, Polyomavirus Infections/diagnosis/*drug therapy/etiology/virology, Tacrolimus/pharmacology, Tumor Virus Infections/diagnosis/*drug therapy/etiology/virology, Virus Activation/drug effects",
author = "Barbara Suwelack and Viola Malyar and Martina Koch and Martina Sester and Claudia Sommerer",
year = "2012",
language = "English",
volume = "26",
pages = "201--211",
number = "3",

}

RIS

TY - JOUR

T1 - The influence of immunosuppressive agents on BK virus risk following kidney transplantation, and implications for choice of regimen.

AU - Suwelack, Barbara

AU - Malyar, Viola

AU - Koch, Martina

AU - Sester, Martina

AU - Sommerer, Claudia

PY - 2012

Y1 - 2012

N2 - The increasing incidence of BK-associated nephropathy following kidney transplantation has prompted an examination of strategies for risk reduction and management through immunosuppression manipulation. Evidence from retrospective and prospective studies suggests that BK viruria and viremia, and the need for BK virus treatment, are higher with tacrolimus than cyclosporine. Combined therapy with tacrolimus and mycophenolic acid may be associated with a particularly higher risk of BK infection, but data are conflicting as to whether mycophenolic acid per se is an independent risk factor. The incidence of BK-related events may be reduced in patients receiving mTOR inhibitors (everolimus or sirolimus) with cyclosporine vs a calcineurin inhibitor with mycophenolic acid. De novo immunosuppression regimens that avoid rabbit antithymocyte globulin and tacrolimus, particularly tacrolimus with mycophenolic acid, may be advantageous, whereas low-exposure cyclosporine with an mTOR inhibitor appears a favorable option. Routine screening for BK infection during the first 2 years posttransplant is recommended to allow preemptive modification of the immunosuppressive regimen. In patients at high risk of BK virus infection, appropriate de novo immunosuppression or very early conversion to an mTOR inhibitor to facilitate reduction or discontinuation of calcineurin inhibitors or antimetabolites should be considered. Extensive further research into optimal avoidance, screening, and treatment strategies is required.

AB - The increasing incidence of BK-associated nephropathy following kidney transplantation has prompted an examination of strategies for risk reduction and management through immunosuppression manipulation. Evidence from retrospective and prospective studies suggests that BK viruria and viremia, and the need for BK virus treatment, are higher with tacrolimus than cyclosporine. Combined therapy with tacrolimus and mycophenolic acid may be associated with a particularly higher risk of BK infection, but data are conflicting as to whether mycophenolic acid per se is an independent risk factor. The incidence of BK-related events may be reduced in patients receiving mTOR inhibitors (everolimus or sirolimus) with cyclosporine vs a calcineurin inhibitor with mycophenolic acid. De novo immunosuppression regimens that avoid rabbit antithymocyte globulin and tacrolimus, particularly tacrolimus with mycophenolic acid, may be advantageous, whereas low-exposure cyclosporine with an mTOR inhibitor appears a favorable option. Routine screening for BK infection during the first 2 years posttransplant is recommended to allow preemptive modification of the immunosuppressive regimen. In patients at high risk of BK virus infection, appropriate de novo immunosuppression or very early conversion to an mTOR inhibitor to facilitate reduction or discontinuation of calcineurin inhibitors or antimetabolites should be considered. Extensive further research into optimal avoidance, screening, and treatment strategies is required.

KW - Humans

KW - Risk Factors

KW - TOR Serine-Threonine Kinases/antagonists & inhibitors

KW - Kidney Transplantation

KW - Calcineurin/antagonists & inhibitors

KW - Virus Replication/drug effects

KW - Antilymphocyte Serum/pharmacology

KW - BK Virus/drug effects/physiology

KW - Glucocorticoids/pharmacology

KW - Immunosuppressive Agents/pharmacology/therapeutic use

KW - Mycophenolic Acid/pharmacology

KW - Polyomavirus Infections/diagnosis/drug therapy/etiology/virology

KW - Tacrolimus/pharmacology

KW - Tumor Virus Infections/diagnosis/drug therapy/etiology/virology

KW - Virus Activation/drug effects

KW - Humans

KW - Risk Factors

KW - TOR Serine-Threonine Kinases/antagonists & inhibitors

KW - Kidney Transplantation

KW - Calcineurin/antagonists & inhibitors

KW - Virus Replication/drug effects

KW - Antilymphocyte Serum/pharmacology

KW - BK Virus/drug effects/physiology

KW - Glucocorticoids/pharmacology

KW - Immunosuppressive Agents/pharmacology/therapeutic use

KW - Mycophenolic Acid/pharmacology

KW - Polyomavirus Infections/diagnosis/drug therapy/etiology/virology

KW - Tacrolimus/pharmacology

KW - Tumor Virus Infections/diagnosis/drug therapy/etiology/virology

KW - Virus Activation/drug effects

M3 - SCORING: Journal article

VL - 26

SP - 201

EP - 211

IS - 3

M1 - 3

ER -