Cellular Immunity to Predict the Risk of Cytomegalovirus Infection in Kidney Transplantation: A Prospective, Interventional, Multicenter Clinical Trial.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
03 12 2020
Historique:
received: 14 06 2019
accepted: 20 12 2019
pubmed: 23 2 2020
medline: 28 4 2021
entrez: 21 2 2020
Statut: ppublish

Résumé

Improving cytomegalovirus (CMV) immune-risk stratification in kidney transplantation is highly needed to establish guided preventive strategies. This prospective, interventional, multicenter clinical trial assessed the value of monitoring pretransplant CMV-specific cell-mediated immunity (CMI) using an interferon-γ release assay to predict CMV infection in kidney transplantation. One hundred sixty donor/recipient CMV-seropositive (D+/R+) patients, stratified by their baseline CMV (immediate-early protein 1)-specific CMI risk, were randomized to receive either preemptive or 3-month antiviral prophylaxis. Also, 15-day posttransplant CMI risk stratification and CMI specific to the 65 kDa phosphoprotein (pp65) CMV antigen were investigated. Immunosuppression consisted of basiliximab, tacrolimus, mycophenolate mofetil, and corticosteroids in 80% of patients, whereas 20% received thymoglobulin induction therapy. Patients at high risk for CMV based on pretransplant CMI developed significantly higher CMV infection rates than those deemed to be at low risk with both preemptive (73.3% vs 44.4%; odds ratio [OR], 3.44 [95% confidence interval {CI}, 1.30-9.08]) and prophylaxis (33.3% vs 4.1%; OR, 11.75 [95% CI, 2.31-59.71]) approaches. The predictive capacity for CMV-specific CMI was only found in basiliximab-treated patients for both preemptive and prophylaxis therapy. Fifteen-day CMI risk stratification better predicted CMV infection (81.3% vs 9.1%; OR, 43.33 [95% CI, 7.89-237.96]). Pretransplant CMV-specific CMI identifies D+/R+ kidney recipients at high risk of developing CMV infection if not receiving T-cell-depleting antibodies. Monitoring CMV-specific CMI soon after transplantation further defines the CMV infection prediction risk. Monitoring CMV-specific CMI may guide decision making regarding the type of CMV preventive strategy in kidney transplantation. NCT02550639.

Sections du résumé

BACKGROUND
Improving cytomegalovirus (CMV) immune-risk stratification in kidney transplantation is highly needed to establish guided preventive strategies.
METHODS
This prospective, interventional, multicenter clinical trial assessed the value of monitoring pretransplant CMV-specific cell-mediated immunity (CMI) using an interferon-γ release assay to predict CMV infection in kidney transplantation. One hundred sixty donor/recipient CMV-seropositive (D+/R+) patients, stratified by their baseline CMV (immediate-early protein 1)-specific CMI risk, were randomized to receive either preemptive or 3-month antiviral prophylaxis. Also, 15-day posttransplant CMI risk stratification and CMI specific to the 65 kDa phosphoprotein (pp65) CMV antigen were investigated. Immunosuppression consisted of basiliximab, tacrolimus, mycophenolate mofetil, and corticosteroids in 80% of patients, whereas 20% received thymoglobulin induction therapy.
RESULTS
Patients at high risk for CMV based on pretransplant CMI developed significantly higher CMV infection rates than those deemed to be at low risk with both preemptive (73.3% vs 44.4%; odds ratio [OR], 3.44 [95% confidence interval {CI}, 1.30-9.08]) and prophylaxis (33.3% vs 4.1%; OR, 11.75 [95% CI, 2.31-59.71]) approaches. The predictive capacity for CMV-specific CMI was only found in basiliximab-treated patients for both preemptive and prophylaxis therapy. Fifteen-day CMI risk stratification better predicted CMV infection (81.3% vs 9.1%; OR, 43.33 [95% CI, 7.89-237.96]).
CONCLUSIONS
Pretransplant CMV-specific CMI identifies D+/R+ kidney recipients at high risk of developing CMV infection if not receiving T-cell-depleting antibodies. Monitoring CMV-specific CMI soon after transplantation further defines the CMV infection prediction risk. Monitoring CMV-specific CMI may guide decision making regarding the type of CMV preventive strategy in kidney transplantation.
CLINICAL TRIALS REGISTRATION
NCT02550639.

Identifiants

pubmed: 32076718
pii: 5686894
doi: 10.1093/cid/ciz1209
doi:

Substances chimiques

Antiviral Agents 0

Banques de données

ClinicalTrials.gov
['NCT02550639']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2375-2385

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Auteurs

Marta Jarque (M)

Experimental Nephrology Laboratory, Bellvitge Biomedical Research Institute, IDIBELL, Hospitalet de Llobregat, Spain.

Elena Crespo (E)

Experimental Nephrology Laboratory, Bellvitge Biomedical Research Institute, IDIBELL, Hospitalet de Llobregat, Spain.

Edoardo Melilli (E)

Kidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.

Alex Gutiérrez (A)

Kidney Transplant Unit, Nephrology Department, Hospital Miguel Servet, Zaragoza, Spain.

Francesc Moreso (F)

Kidney Transplant Unit, Nephrology Department, Vall d'Hebrón University Hospital, Barcelona, Spain.

Lluís Guirado (L)

Kidney Transplant Unit, Nephrology Department, Fundació Puigvert, Barcelona, Spain.

Ignacio Revuelta (I)

Kidney Transplant Unit, Nephrology Department, Hospital Clínic de Barcelona, Barcelona, Spain.

Nuria Montero (N)

Kidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.

Joan Torras (J)

Experimental Nephrology Laboratory, Bellvitge Biomedical Research Institute, IDIBELL, Hospitalet de Llobregat, Spain.
Kidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.

Lluís Riera (L)

Urology Department, Bellvitge University Hospital, Barcelona, Spain.

Maria Meneghini (M)

Experimental Nephrology Laboratory, Bellvitge Biomedical Research Institute, IDIBELL, Hospitalet de Llobregat, Spain.
Kidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.

Omar Taco (O)

Kidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.

Anna Manonelles (A)

Kidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.

Javier Paul (J)

Kidney Transplant Unit, Nephrology Department, Hospital Miguel Servet, Zaragoza, Spain.

Daniel Seron (D)

Kidney Transplant Unit, Nephrology Department, Vall d'Hebrón University Hospital, Barcelona, Spain.

Carme Facundo (C)

Kidney Transplant Unit, Nephrology Department, Fundació Puigvert, Barcelona, Spain.

Josep M Cruzado (JM)

Experimental Nephrology Laboratory, Bellvitge Biomedical Research Institute, IDIBELL, Hospitalet de Llobregat, Spain.
Kidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.

Salvador Gil Vernet (S)

Kidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.

Josep M Grinyó (JM)

Experimental Nephrology Laboratory, Bellvitge Biomedical Research Institute, IDIBELL, Hospitalet de Llobregat, Spain.
Kidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.

Oriol Bestard (O)

Experimental Nephrology Laboratory, Bellvitge Biomedical Research Institute, IDIBELL, Hospitalet de Llobregat, Spain.
Kidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.

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