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Mesenchymal Stem Cell Transplantation in the Treatment of Chronic Antibody Mediated Kidney Graft Rejection (ABMR)

Autologous Mesenchymal Stem Cell Transplantation in the Treatment of Chronic Antibody Mediated Kidney Graft Rejection (ABMR)

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03585855
Enrollment
4
Registered
2018-07-13
Start date
2019-01-01
Completion date
2019-07-23
Last updated
2019-07-25

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

Conditions

Interventional

Brief summary

Transplant rejection is one of the biggest limitations in renal transplant procedures, where the kidney can undergo an acute, late acute, or chronic transplant rejection. With the advancement in transplantation protocols, acute survival of renal transplants has improved, but long-term survival is still unsatisfactory, as most of the renal transplants develop chronic graft rejection. Unfortunately, there is little the investigators know when it comes to improving long-term survival of renal transplants. Mesenchymal stem cells (MSC) have been shown to have immunosuppressive and repairing properties. The purpose of this study is to find out whether MSC in combination with standard therapy of antibody mediated rejection (ABMR) are more effective in preventing organ deterioration and maintaining kidney function.

Detailed description

Participants will be assigned to receive the full immunosuppressive therapy indicated to treat chronic ABMR (including plasmapheresis (PF) 7x, intravenous immune globulins 100 mg/kg 7x, corticosteroid) and MSC infusions (2x106cells/kg bw after PF) (Group 1) and be compared to historic controls according to propensity score matching (treated with immunosuppressive therapy alone (Group 2)). Patients will undergo MSC infusions at the start of the study after each PF. One year post- infusions, patients will be evaluated and undergo kidney biopsies. Blood collection will occur at regular intervals, serum creatinine and the estimated creatinine clearance will be monthly recorded. The transplanted kidney function and morphology (US Doppler) will be evaluated.

Interventions

MSC transplantation: patients with ABMR treated with MSC transplantation

Sponsors

Slovenian Research Agency
CollaboratorOTHER
University Medical Centre Ljubljana
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

comparison with historic control

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Recipients of a renal allograft, male and female patients age \>18 * The eGF\>20 ml/min/1.73 m2, * Renal biopsy Criteria: chronic active ABMR. * Written informed consent, compliant with local regulations.

Exclusion criteria

* Recipients of multiple organs. * Pregnant women. * Malignant disease in last 5 years * Active autoimmune disease * Active infection including hepatitis B, hepatitis C, HIV, or tuberculosis * Evidence of congestive cardiac failure and/or acute coronary syndrome in past 6 months. * Evidence of liver disease * Inadequate compliance to treatment.

Design outcomes

Primary

MeasureTime frameDescription
Safety of MSC transplantation as assessed by adverse events according to CTCAE Version 5Estimated glomerular filtration rate (eGFR)12 monthsAdverse events according to CTCAE Version 5

Secondary

MeasureTime frameDescription
Estimated glomerular filtration rate (eGFR)12 monthseGFR at up to 12 months post MSC transplantation
Graft survival rate12 monthsGraft survival rate at 12 months post MSC transplantation

Countries

Slovenia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026