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

Author:

Jarque Marta1,Crespo Elena1,Melilli Edoardo2ORCID,Gutiérrez Alex3,Moreso Francesc4,Guirado Lluís5,Revuelta Ignacio6,Montero Nuria2,Torras Joan12,Riera Lluís7,Meneghini Maria12,Taco Omar2,Manonelles Anna2,Paul Javier3,Seron Daniel4,Facundo Carme5,Cruzado Josep M12,Gil Vernet Salvador2,Grinyó Josep M12,Bestard Oriol12

Affiliation:

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

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

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

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

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

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

7. Urology Department, Bellvitge University Hospital, Barcelona, Spain

Abstract

Abstract 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.

Funder

Instituto de Salud Carlos III

European Union’s Horizon 2020 research and innovation program

Biomarker-Driven Immunosuppression Minimization (BIODRIM) Consortium

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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