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Immune Monitoring of Prevalent Kidney Transplant Recipients Using Torque Teno Virus: A Single-Center, Prospective Cohort Study

Immune Monitoring of Prevalent Kidney Transplant Recipients Using Torque Teno Virus: A Single-Center, Prospective Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05836636
Acronym
TTV-KTR-SGH
Enrollment
172
Registered
2023-05-01
Start date
2023-06-27
Completion date
2025-07-31
Last updated
2026-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Kidney Transplant; Complications, Kidney Transplant Infection, Kidney Transplant Rejection

Brief summary

Kidney transplant recipients (KTRs) suffer from immunosuppression-related adverse events (iRAEs), such as infections and malignancy from chronic immunosuppression exposure but are also at risk of graft loss from rejection with under-immunosuppression. Biomarkers that predict both iRAEs and rejection and allow individualisation of immunosuppression exposure are lacking. While plasma viral DNA levels of Torque Teno Virus (TTV), a widely prevalent, non-pathogenic virus, have been shown to predict both iRAE and rejection in incident KTRs within 1 year after transplant, its role for prevalent KTRs on stable immunosuppression is unclear. The investigators hypothesise that plasma TTV levels can predict iRAEs and rejection in KTRs on stable immunosuppression and propose a pilot study to pursue three specific aims: (1) To determine the TTV levels and its relationship with clinical factors affecting the 'net state of immunosuppression' in prevalent KTRs. (2) To analyse the prognostic value of TTV levels for iRAEs and rejection in prevalent KTRs. (3) To compare the prognostic performance of TTV levels to commonly available biomarkers and composite prognostic scores. The investigators seek pursue these aims by performing a single-centre, prospective, observational cohort study of 172 KTRs on stable immunosuppression for more than 3 months. TTV levels will be measured, using the TTV R-GENE® kit, upon recruitment and when kidney allograft biopsies are performed. Subjects will be monitored for iRAEs and rejection for at least 12 months. The study will provide data on the distribution of TTV levels in a prevalent cohort of KTRs and analyse its relationship with clinical factors and important clinical outcomes. If the study indicates that TTV may be predictive of iRAEs and rejection, the investigators aim to conduct further studies including interventional studies using TTV levels to guide immunosuppression. Ultimately, the investigators aim to use TTV as a biomarker to optimise long-term immunosuppression exposure, reduce the risk of iRAEs without increase in rejection, and improve long-term outcomes for KTRs.

Interventions

OTHERTorque teno virus DNA measurement

Torque teno virus DNA level will be obtained from all study subjects upon recruitment, when subjects are admitted and when subjects undergo kidney allograft biopsies.

Sponsors

Singapore General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Kidney transplant recipients on follow up at Singapore General Hospital (SGH) * More than 21 years old * On stable doses of immunosuppression for more than 3 months

Exclusion criteria

* Titration of immunosuppression (e.g. for rejection or infection) less than 3 months ago * Active infection requiring treatment * Less than 21 years old * Unable to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Severe infections defined as any infection requiring hospitalization1 yearAny infection requiring hospitalization

Secondary

MeasureTime frameDescription
Opportunistic infections1 yearintracellular bacteria, mycobacteria, Listeria monocytogenes, and Nocardia spp., herpesviruses (CMV, HSV, and VZV), polyomaviruses, yeasts (Candida and Cryptococcus), molds (invasive aspergillosis and mucormycosis), and parasites (Toxoplasma gondii, PJP, and Leishmania)
De novo malignancy1 yearDe novo malignancy
Calcineurin inhibitor nephrotoxicity (biopsy-proven)1 yearCalcineurin inhibitor nephrotoxicity (biopsy-proven)
Rejection (biopsy-proven)1 yearWith and without borderline T cell-mediated rejection
Glomerulonephritis - de novo or recurrent (biopsy-proven)1 year
Graft function1 yearserum creatinine, estimated glomerular filtration rate by the CKD-EPI equation and urine protein-to-creatinine ratio
Graft loss1 yearCensored and non-censored for death
Mortality1 yearAll-cause and cause-specific - i.e., infection, malignancy, cardiovascular, others
Immunosuppression-related adverse event1 yearComposite outcome of severe infections defined as any infection requiring hospitalization, opportunistic infections, de novo malignancy and calcineurin inhibitor nephrotoxicity
Immune-mediated adverse event1 yearComposite outcome of rejection (biopsy-proven) and glomerulonephritis (biopsy-proven)

Countries

Singapore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 30, 2026