Mesenchymal Stem Cells and Subclinical Rejection

Organ Transplantation Clinical Trial

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Official title:

Bone Marrow Derived Mesenchymal Stem Cells for the Treatment of Allograft Rejection After Renal Transplantation

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00734396
• Other study ID #: P08.119
• Secondary ID: NL21298.000.08
• Status: Completed
• Phase: Phase 1/Phase 2
• First received: August 13, 2008
• Last updated: January 4, 2013
• Start date: February 2009
• Est. completion date: December 2012

Study information

• Verified date: January 2013
• Source: Leiden University Medical Center
• Contact: n/a
• Is FDA regulated: No
• Health authority: Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
• Study type: Interventional

Clinical Trial Summary

The purpose of the study is to test the safety and feasibility of autologous mesenchymal stem cell therapy in HLA-DR mismatched patients with subclinical rejection and or an increase in IF?TA in the renal biopsy 4 weeks or 6 months after renal transplantation.

Description:

Kidney transplantation has improved survival and quality of life for patients with end-stage organ failure. Despite dramatic improvements in short-term survival, long-term survival of renal allografts has changed little during the past decade. Recently, it has been demonstrated that chronic lesions originate already very early after transplantation and that subclinical rejection (SCR) in protocol biopsies is a risk factor for late graft loss. However the efficacy of high-dose corticosteroids and other therapies for the treatment of SCR have been shown to be inadequate. Thus, despite the availability of a range of available medications there remains a need for therapeutic alternatives because patients may not respond to existing therapeutic choices, they do not show an improvement of the fibrosis reaction or an effect on long term survival, or they may develop immunosuppression induced serious (sometimes fatal) side effects and toxicities.

In recent years it has become evident that bone marrow (BM) derived mesenchymal stem cells have potent immunomodulatory effects. MSCs are pluripotent cells that can differentiate into several mesenchymal tissues, including fibroblasts, osteoblasts, adipocytes and chondrocyte progenitors. MSCs have potent immunosuppressive effects on T and B cells in vitro and in animal models of chronic inflammation. Encouraging results have been obtained in patients with steroid resistant acute and severe Graft versus Host Disease (GvHD). The investigators hypothesize that infusion of MSCs may similarly provide a novel treatment option in the treatment of patients with allograft rejection with less side effects than existing immunosuppressive therapies.This study will evaluate the safety and feasibility of MSC therapy in renal recipients.

In total 15 de novo renal recipients of 2 HLA-DR mismatched living donors, men and women, 18-65 years of age, will be recruited from the renal transplant clinics of the LUMC. Only patients with SCR abd or an increase in IF/TA in the protocol biopsy 4 weeks or 6 months after transplantation will receive MSC infusions. MSCs from patients without SCR in their biopsy will be only used for feasibility and function studies (as described earlier). Subjects will receive two doses of 1 x 10.6 MSCs per kilogram body weight, intravenously, 7 days apart. The investigators will investigate safety of MSC therapy by assessing the rate of (serious) adverse events in the study population using the World Health Organization (WHO) criteria. Feasibility will be obtained by determining the number of expanded MSCs in relation to the amount of BM collected, number of passages required and time to reach study target doses.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 15
• Est. completion date: December 2012
• Est. primary completion date: March 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Subject is willing to participate in the study and has signed the informed consent.

• Recipients of a first kidney graft from a living HLA-DR mismatched donor (2 HLA-DR mismatches).

• Subjects included in the study must have kidney biopsy proven SCR 4 weeks after transplantation.

• Patients must be on triple immunosuppressive therapy of prednisone, CsA or tacrolimus and MMF according to current protocol.

• Panel Reactive Antibodies (PRA) = 5%.

• Patients must be able to adhere to the study visit schedule and protocol requirements.

• If female and of child-bearing age, subject must be non-pregnant, non-breastfeeding, and use adequate contraception.

• Patients must be able to give informed consent and the consent must be obtained prior to any study procedure.

Exclusion Criteria:

• Double organ transplant recipient.

• Acute clinical rejection after transplantation.

• Patients with evidence of active infection or abcesses before MSC infusion.

• Patients suffering from hepatic failure.

• Patients suffering from an active autoimmune disease.

• Patients who have had a previous BM transplant.

• A psychiatric, addictive or any disorder that compromises ability to give truly informed consent for participation in this study.

• Use of any investigational drug after transplantation.

• Documented HIV infection, active hepatitis B, hepatitis C or TB according to current transplantation inclusion criteria.

• Subjects who currently have an active opportunistic infection (e.g., herpes zoster [shingles], cytomegalovirus (CMV), Pneumocystis carinii (PCP), aspergillosis, histoplasmosis, or mycobacteria other than TB) after transplantation.

• Malignancy (including lymphoproliferative disease) within the past 2-5 years (except for squamous or basal cell carcinoma of the skin that has been treated with no evidence of recurrence) according to current transplantation inclusion criteria.

• Known recent substance abuse (drug or alcohol).

• Contraindications to undergo a BM biopsy.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Organ Transplantation

Intervention

Procedure:
• Mesenchymal stem cell infusion
MSC infusion: two doses of 1-2x106 MSCs per kilogram body weight, intravenously, 7 days apart.

Locations

Country	Name	City	State
Netherlands	Leiden Universitary Medical Center	Leiden

Sponsors (1)

Lead Sponsor	Collaborator
Leiden University Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Primary 1 Safety: rate of (serious) adverse events in the study population 2 Feasibility: determination of the number of expanded MSCs in relation to the amount of BM collected, number of passages required and time to reach study target doses		2 years	Yes
Secondary	Secondary endpoints: 1 Presence of late acute rejection (in the 6 month biopsy compared with the 4 week biopsy). 2 Sirius red staining for renal cortical matrix accumulation. 3 Immunologic response before and after MSC infusion.		2 years	Yes