Urinary Tract, Sexual Organs, and Pregnancy Conditions

All Conditions

Digestive System Diseases

Symptoms and General Pathology

Kidney Diseases

Renal Insufficiency

Liver Cirrhosis

Liver Failure

Hepatic Insufficiency

Liver Diseases

Liver Failure, Acute

Urologic Diseases

Urogenital Diseases

Female Urogenital Diseases

Pregnancy Complications

Female Urogenital Diseases and Pregnancy Complications

Male Urogenital Diseases

Gastrointestinal Diseases

Anti-Infective Agents

All Drugs and Chemicals

Antineoplastic Agents

Hematinics

Anti-Bacterial Agents

Antibodies

Mycophenolic Acid

Tacrolimus

Immunoglobulins

Liver Extracts

Immunosuppressive Agents

Patients undergoing a first liver transplantation. Beside receiving standard liver tranplantation care (antibacterial and viral prophylactic treatments as well as a standard immunosuppressive regime i.e. tacrolimus, mycophenolate mofetil and steroids), patients will be infused with 1,5-3,0 10E6 MSC/kg on postoperative day 3+/-2

Patients undergoing a first kidney transplantation. Beside receiving standard kidney tranplantation care (antibacterial and viral prophylactic treatments as well as a standard immunosuppressive regime i.e. tacrolimus, mycophenolate mofetil and steroids associated with ant-IL-2 antibodies), patients will be infused with 1,5-3,0 10E6 MSC/kg on postoperative day 3+/-2.

Third party MSC 1,5-3,010E6/kg. No HLA matching between MSC donor and the recipient or the liver/kidney donor. One infusion at day 3+/-2.

Mesenchymal Stem Cells

Yves Beguin, MD, PhD

The immune system of a patient can attack the liver or the kidney received from a donor (organ rejection). This can be prevented by treating these patients long-life with immunosuppressive drugs. Unfortunately, these drugs lead to numerous side effects and fail to prevent the rejection occurring months later after the transplantation (chronic rejection). Recently, it has been shown that a particular type of cells present in the bone marrow, namely Mesenchymal Stem Cells (MSC), when injected to a patient, suppress its immune system and increase success rates of blood cells transplantation. This outcome opens doors to investigate the potential of these cells to provide a valuable tool for improving solid organ transplantation without the need of high concentration of immunosuppressive drugs. The present project aims at evaluating the safety and tolerability of MSC administration after liver or kidney transplantation.

The present project aims at evaluating the safety and tolerability of third party MSC administration after liver or kidney organ transplantation. Ten patients undergoing liver transplantation and 10 patients undergoing kidney transplantation will be included in the experimental arm to receive a single infusion of MSC. The outcome of each of these 2 subgroups will be compared with that of similar control patients undergoing liver or kidney transplantation but who will not receive MSC.

Liver and kidney transplanted patients will receive standard immunosuppressive therapy, TAC-MMF-steroïds and TAC-MMF-steroïds plus an IL-2-R antibody respectively. Patients enrolled in the experimental arms will be infused with a single dose of 1,5-3,0 10E6 MSC/kg, 3(+/-2) days after the transplantation.

Weaning of immunosuppression will be attempted from month 6 in liver transplant patients who did not present a rejection episode and show normal graft function and graft biopsy.

Kidney transplant patients will continue standard immunosuppressive therapy indefinitely.

Male or female (\>18 years) individuals unrelated to the recipient or the graft donor will be MSC donors. MSC donors need to fulfill generally accepted criteria for allogeneic HSC donation.

Mesenchymal Stem Cells After Renal or Liver Transplantation

Infusion of Third-party Mesenchymal Stem Cells After Renal or Liver Transplantation. A Phase I-II, Open-label, Clinical Study

Incidence, timing and severity of any clinical complication related to MSC infusion, including pulmonary events or immune reactions.

* Incidence, timing and severity of any infection (bacterial, viral, fungal, parasitic) (blood hemoculture, urine culture, PCR CMV, PCR BK virus at month 1,2,3)
* Incidence, timing and severity of malignant disease (Posttransplant lymphoproliferative disorder or other)

* Liver Transplantation: bilirubin, INR, transaminases, GGT, at day 7, months 1, 3, 6, 9, 12.
* Kidney Transplanttaion: number of post transplant hemodialysis, creatinine at day 7, months 1, 3, 6, 9, 12.

To evaluate recipient's immune function (T cell blood populations (including T regs) by FACS, TREC quantification, Vβ repertoire diversity, pathogen-specific T cells, anti-organ donor HLA antibodies).

To evaluate the potential development of anti-MSC donor HLA antibodies.

Study title	NCT ID	Conditions	Interventions	Eligibility	Organization
Mesenchymal Stem Cells After Renal or Liver Transplantation	NCT01429038	Liver Failure Kidney Failure	Mesenchymal Ste...	18 Years - 75 Years	University of Liege
Mesenchymal Stem Cells After Renal or Liver Transplantation	NCT01429038	Liver Failure Kidney Failure	Mesenchymal Ste...	18 Years - 75 Years	University of Liege
Mesenchymal Stem Cells After Renal or Liver Transplantation	NCT01429038	Liver Failure Kidney Failure	Mesenchymal Ste...	18 Years - 75 Years	University of Liege

Spots Global Cancer Trial Database for metabolic hepatic diseases