CMV Reactivation, CMV Specific Immune Response, Kidney Transplant, Kidney Transplant Recipient
Conditions
Keywords
CMV, Kidney Transplantation, QuantiFERON-CMV, Solid Organ Transplantation
Brief summary
The goal of this observational study is to identify risk factors associated with the absence of CMV-specific cellular immune response in low-risk CMV-seropositive kidney transplant recipients in the early post-transplant period. The participant population includes adult CMV-seropositive kidney transplant recipients who did not receive antithymocyte globulin (ATG) induction therapy and underwent QuantiFERON-CMV testing within the first 45 days after transplantation. The main question it aims to answer is: \- Is it possible to predict which patients will fail to develop a CMV-specific cellular immune response before day 45 post-transplant in the absence of directly available immune assessment techniques? Researchers will compare patients with reactive QuantiFERON-CMV results to patients with non-reactive or indeterminate results to identify factors associated with the absence of CMV-specific cellular immune response. Participants will have retrospective clinical and laboratory data collected from medical records.
Detailed description
Study Hypothesis: In the absence of available techniques to assess CMV-specific cellular immunity, it may be possible to predict which patients will fail to develop a CMV-specific cellular immune response before day 45 post-transplant. Objective: Primary objective: * Derivation Cohort: To evaluate the risk factors associated with a non-reactive or indeterminate QF-CMV result before day 45 post-transplant in CMV-seropositive (R⁺) recipients who did not receive ATG prophylaxis. * Validation Cohort: To validate these risk factors in an independent validation cohort. Secondary Objectives: * To confirm whether patients with a non-reactive or indeterminate QF-CMV result before day 45 post-transplant and without ATG induction develop a higher rate of clinically significant CMV infection compared with those with a reactive QF-CMV result during the first 6 months post-transplant. * To confirm whether these same patients present a higher rate of viral replication during the first 6 months post-transplant. Study Population: The study will include adult patients (\>18 years) who are CMV-seropositive (R⁺), received a kidney transplant during the study period, did not receive ATG prophylaxis, and underwent QF-CMV testing on day 45 post-transplant (with a window period between day 30 and day 60 post-transplant).
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* Age \>18 years * Kidney or pancreas-kidney transplant recipients with positive CMV serology * QF-CMV test performed on day 45 post-transplant (window period between day 30 and day 60 post-transplant) * CMV PCR testing performed at least every two weeks during the first three months post-transplant
Exclusion criteria
* HIV-infected patients * Multivisceral transplant recipients * Patients scheduled to receive universal prophylaxis despite having a reactive QF-CMV result * Patients who received ATG induction therapy * Less than 6 months of post-transplant follow-up
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Risk factors associated with a non-reactive or indeterminate QF-CMV | Between 15 and 45 days after kidney transplantation | Absence of CMV-specific cellular immune response assessed by early QuantiFERON-CMV testing |
Countries
Spain