Viral load kinetics and the clinical consequences of cytomegalovirus in kidney transplantation

BackgroundDespite advances in clinical management, cytomegalovirus (CMV) infection remains a serious complication and an important cause of morbidity and mortality following kidney transplantation. Here, we explore the importance of viral load kinetics as predictors of risk and potential guides to t...

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Main Authors: Sabina Dobrer, Karen R. Sherwood, Ishan Hirji, James Lan, John Gill, Nancy Matic, Paul A. Keown
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-01-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2023.1302627/full
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author Sabina Dobrer
Karen R. Sherwood
Ishan Hirji
James Lan
James Lan
John Gill
Nancy Matic
Paul A. Keown
Paul A. Keown
author_facet Sabina Dobrer
Karen R. Sherwood
Ishan Hirji
James Lan
James Lan
John Gill
Nancy Matic
Paul A. Keown
Paul A. Keown
author_sort Sabina Dobrer
collection DOAJ
description BackgroundDespite advances in clinical management, cytomegalovirus (CMV) infection remains a serious complication and an important cause of morbidity and mortality following kidney transplantation. Here, we explore the importance of viral load kinetics as predictors of risk and potential guides to therapy to reduce transplant failure in a large longitudinal Genome Canada Transplant Consortium (GCTC) kidney transplant cohort.MethodsWe examined the relationship between CMV infection rates and clinical characteristics, CMV viral load kinetics, and graft and patient outcomes in 2510 sequential kidney transplant recipients in the British Columbia Transplant Program. Transplants were performed between January 1, 2008, and December 31, 2018, were managed according to a standard protocol, and were followed until December 31, 2019, representing over 3.4 million days of care.ResultsLongitudinal CMV testing was performed in 2464 patients, of whom 434 (17.6%) developed a first episode of CMV viremia at a median of 120 (range: 9–3906) days post-transplant. Of these patients, 93 (21.4%) had CMV viremia only and 341 (78.6%) had CMV viremia with clinical complications, of whom 21 (4.8%) had resulting hospitalization. A total of 279 (11.3%) patients died and 177 (7.2%) patients lost their graft during the 12 years of follow-up. Patients with CMV infection were at significantly greater risk of graft loss (p=0.0041) and death (p=0.0056) than those without. Peak viral load ranged from 2.9 to 7.0 (median: 3.5) log10 IU/mL, the duration of viremia from 2 to 100 (15) days, and the viral load area under the curve from 9.4 to 579.8 (59.7) log10 IU/mL × days. All three parameters were closely inter-related and were significantly increased in patients with more severe clinical disease or with graft loss (p=0.001). Duration of the first CMV viremic episode greater than 15 days or a peak viral load ≥4.0 log10 IU/mL offered simple predictors of clinical risk with a 3-fold risk of transplant failure.ConclusionViral load kinetics are closely related to CMV severity and to graft loss following kidney transplantation and provide a simple index of risk which may be valuable in guiding trials and treatment to prevent transplant failure.
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spelling doaj.art-5daa1d520b18472c896c0de43b03c6c92024-02-01T07:49:01ZengFrontiers Media S.A.Frontiers in Immunology1664-32242024-01-011410.3389/fimmu.2023.13026271302627Viral load kinetics and the clinical consequences of cytomegalovirus in kidney transplantationSabina Dobrer0Karen R. Sherwood1Ishan Hirji2James Lan3James Lan4John Gill5Nancy Matic6Paul A. Keown7Paul A. Keown8Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, CanadaDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, CanadaGlobal Evidence and Outcomes, Takeda Development Center Americas, Inc., Lexington, MA, United StatesDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, CanadaDepartment of Medicine, University of British Columbia, Vancouver, BC, CanadaDepartment of Medicine, University of British Columbia, Vancouver, BC, CanadaDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, CanadaDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, CanadaDepartment of Medicine, University of British Columbia, Vancouver, BC, CanadaBackgroundDespite advances in clinical management, cytomegalovirus (CMV) infection remains a serious complication and an important cause of morbidity and mortality following kidney transplantation. Here, we explore the importance of viral load kinetics as predictors of risk and potential guides to therapy to reduce transplant failure in a large longitudinal Genome Canada Transplant Consortium (GCTC) kidney transplant cohort.MethodsWe examined the relationship between CMV infection rates and clinical characteristics, CMV viral load kinetics, and graft and patient outcomes in 2510 sequential kidney transplant recipients in the British Columbia Transplant Program. Transplants were performed between January 1, 2008, and December 31, 2018, were managed according to a standard protocol, and were followed until December 31, 2019, representing over 3.4 million days of care.ResultsLongitudinal CMV testing was performed in 2464 patients, of whom 434 (17.6%) developed a first episode of CMV viremia at a median of 120 (range: 9–3906) days post-transplant. Of these patients, 93 (21.4%) had CMV viremia only and 341 (78.6%) had CMV viremia with clinical complications, of whom 21 (4.8%) had resulting hospitalization. A total of 279 (11.3%) patients died and 177 (7.2%) patients lost their graft during the 12 years of follow-up. Patients with CMV infection were at significantly greater risk of graft loss (p=0.0041) and death (p=0.0056) than those without. Peak viral load ranged from 2.9 to 7.0 (median: 3.5) log10 IU/mL, the duration of viremia from 2 to 100 (15) days, and the viral load area under the curve from 9.4 to 579.8 (59.7) log10 IU/mL × days. All three parameters were closely inter-related and were significantly increased in patients with more severe clinical disease or with graft loss (p=0.001). Duration of the first CMV viremic episode greater than 15 days or a peak viral load ≥4.0 log10 IU/mL offered simple predictors of clinical risk with a 3-fold risk of transplant failure.ConclusionViral load kinetics are closely related to CMV severity and to graft loss following kidney transplantation and provide a simple index of risk which may be valuable in guiding trials and treatment to prevent transplant failure.https://www.frontiersin.org/articles/10.3389/fimmu.2023.1302627/fullkidney transplantcytomegalovirusCMVviral load kineticsclinical outcomes
spellingShingle Sabina Dobrer
Karen R. Sherwood
Ishan Hirji
James Lan
James Lan
John Gill
Nancy Matic
Paul A. Keown
Paul A. Keown
Viral load kinetics and the clinical consequences of cytomegalovirus in kidney transplantation
Frontiers in Immunology
kidney transplant
cytomegalovirus
CMV
viral load kinetics
clinical outcomes
title Viral load kinetics and the clinical consequences of cytomegalovirus in kidney transplantation
title_full Viral load kinetics and the clinical consequences of cytomegalovirus in kidney transplantation
title_fullStr Viral load kinetics and the clinical consequences of cytomegalovirus in kidney transplantation
title_full_unstemmed Viral load kinetics and the clinical consequences of cytomegalovirus in kidney transplantation
title_short Viral load kinetics and the clinical consequences of cytomegalovirus in kidney transplantation
title_sort viral load kinetics and the clinical consequences of cytomegalovirus in kidney transplantation
topic kidney transplant
cytomegalovirus
CMV
viral load kinetics
clinical outcomes
url https://www.frontiersin.org/articles/10.3389/fimmu.2023.1302627/full
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