Clinical Trials Directory

Trials / Completed

CompletedNCT02633826

Pre-formed Alloreactivity in Renal Transplant Recipients

The Role of Pre-formed Alloreactive T Cells on Acute Rejection Episodes and Long-term Graft Outcome in Patients After Living Donor Renal Transplantation

Status
Completed
Phase
Study type
Observational
Enrollment
190 (actual)
Sponsor
Martina Sester · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

This investigator-initiated study will analyse the role of pre-formed alloreactive T cells on acute rejection episodes and graft outcome in kidney transplant recipients after living donation.

Detailed description

In recipients of solid organ transplants, preformed alloreactive T cells may mediate acute rejections and compromise long-term graft survival. Previous studies on the role of alloreactive T cells in transplantation were hampered by the fact that experimental assays to quantify alloreactivity were technically demanding and not suitable for use in a clinical setting. Based on a recent development of a whole-blood assay, alloreactive T cells may be quantified and characterised within one day. This assay therefore provides the experimental basis to study the development and the role of alloreactive T cells in a clinical setting in patients after renal transplantation. This will be performed in a multicenter study in living donor renal transplant recipients where preformed alloreactivity of the recipient towards the living donor will be determined and associated with standard clinical parameters of graft function and long-term graft outcome on follow-up. In addition, the development of donor-specific antibodies will be analysed after transplantation. If this project was able to provide evidence for a role of alloreactive T cells in acute rejection episodes or long-term graft function, this assay may in future be used to guide individualized immunosuppressive drug treatment early after transplantation. It will thereby aid in distinguishing patients where standard immunosuppressive drug regimens are sufficient from the minor population of patients at high risk for rejection who will benefit from intensified drug regimens.

Conditions

Timeline

Start date
2015-11-01
Primary completion
2023-03-01
Completion
2023-03-01
First posted
2015-12-17
Last updated
2024-04-19

Locations

13 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT02633826. Inclusion in this directory is not an endorsement.