Evidence map›Paper›PMID 32076718›Full record

Trial reportClinical infectious diseases : an official publication of the Infectious Diseases Society of America2020

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

Marta Jarque, Elena Crespo, Edoardo Melilli, Alex Gutiérrez, Francesc Moreso, Lluís Guirado, Ignacio Revuelta, Nuria Montero, Joan Torras, Lluís Riera and 10 more

Registry-linked trialAbstract readMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02550639 (A Prospective Randomized Study for Predicting Human Cytomegalovirus), which is not on this map. Cited by 48 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 3 pooled it
5.4field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02550639 phase4completednot on this map

A Prospective Randomized Study for Predicting Human Cytomegalovirus (hCMV) Infection According to Baseline hCMV-specific T-cell Response in Kidney Transplant Patients (RESPECT)

TypeinterventionalSponsorORIOL BESTARDRan2014 to 2018Enrolled160ConditionsCMV Infection, Kidney TransplantationArmsBIOMARKER- elispot test
3 · Its place in the literature

Who cites it

48 citing papers in PubMed, 3 syntheses or guidelines pooled it, 88 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Mechanisms and Determinants of CMV Reactivation in Kidney Transplantation.International journal of molecular sciences · 2026
    Review
  6. Article
  7. Article
  8. "Innovative diagnostics and treatments of infections in transplantation," report from the 2025Transplant international : official journal of the European Society for Organ Transplantation · 2026
    Article
  9. Article
  10. Current and Future Strategies for the Prevention and Treatment of Cytomegalovirus Infections in Transplantation.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Effector-Memory γδ T Lymphocytes Predict CMV Disease After the Withdrawal of Prophylaxis in Kidney Transplant Recipients.Transplant international : official journal of the European Society for Organ Transplantation · 2025
    Article
  18. Advancements in Cytomegalovirus Management Among Solid Organ Transplant Recipients: Insights From the ESOT CMV Workshop 2023.Transplant international : official journal of the European Society for Organ Transplantation · 2025
    Article
  19. Article
  20. Protocol for the ELISPOT-TC Trial: A Randomized Controlled Study Evaluating CMV-Specific Cellular Immune Monitoring in Heart Transplant Recipients.Transplant international : official journal of the European Society for Organ Transplantation · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 6 institutions in 2 countries.

Marta JarqueExperimental Nephrology Laboratory, Bellvitge Biomedical Research Institute, IDIBELL, Hospitalet de Llobregat, Spain.
Elena CrespoExperimental Nephrology Laboratory, Bellvitge Biomedical Research Institute, IDIBELL, Hospitalet de Llobregat, Spain.
Edoardo MelilliKidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.
Alex GutiérrezKidney Transplant Unit, Nephrology Department, Hospital Miguel Servet, Zaragoza, Spain.
Francesc MoresoKidney Transplant Unit, Nephrology Department, Vall d'Hebrón University Hospital, Barcelona, Spain.
Lluís GuiradoKidney Transplant Unit, Nephrology Department, Fundació Puigvert, Barcelona, Spain.
Ignacio RevueltaKidney Transplant Unit, Nephrology Department, Hospital Clínic de Barcelona, Barcelona, Spain.
Nuria MonteroKidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.
Joan TorrasExperimental Nephrology Laboratory, Bellvitge Biomedical Research Institute, IDIBELL, Hospitalet de Llobregat, Spain.
Lluís RieraUrology Department, Bellvitge University Hospital, Barcelona, Spain.
Maria MeneghiniExperimental Nephrology Laboratory, Bellvitge Biomedical Research Institute, IDIBELL, Hospitalet de Llobregat, Spain.
Omar TacoKidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.
Anna ManonellesKidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.
Javier PaulKidney Transplant Unit, Nephrology Department, Hospital Miguel Servet, Zaragoza, Spain.
Daniel SeronKidney Transplant Unit, Nephrology Department, Vall d'Hebrón University Hospital, Barcelona, Spain.
Carme FacundoKidney Transplant Unit, Nephrology Department, Fundació Puigvert, Barcelona, Spain.
Josep M CruzadoExperimental Nephrology Laboratory, Bellvitge Biomedical Research Institute, IDIBELL, Hospitalet de Llobregat, Spain.
Salvador Gil VernetKidney Transplant Unit, Nephrology Department, Bellvitge University Hospital, Barcelona, Spain.
Josep M GrinyóExperimental Nephrology Laboratory, Bellvitge Biomedical Research Institute, IDIBELL, Hospitalet de Llobregat, Spain.
Oriol BestardExperimental Nephrology Laboratory, Bellvitge Biomedical Research Institute, IDIBELL, Hospitalet de Llobregat, Spain.
Bellvitge University Hospital · ESHebron University · PSHospital Universitario Miguel Servet · ESInstitut d'Investigació Biomédica de Bellvitge · ESPuigvert Foundation · ESHospital Clínic de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImproving cytomegalovirus (CMV) immune-risk stratification in kidney transplantation is highly needed to establish guided preventive strategies.

methodsThis 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.

resultsPatients 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]).

conclusionsPretransplant 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.

Indexed as

Cytomegalovirus InfectionsKidney TransplantationAntiviral AgentsCytomegalovirusHumansImmunity, CellularProspective StudiesAntiviral Agentscell-mediated immunitycytomegalovirusimmune monitoringkidney transplantation

Identifiers

PMID32076718
OpenAlexW3007692976

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.