Allogeneic Mesenchymal Stromal Cell Therapy in Renal Transplant Recipients

Rejection Clinical Trial

— Neptune  

Official title:

Safety of Allogeneic Bone Marrow Derived Mesenchymal Stromal Cell Therapy in Renal Transplant Recipients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02387151
• Other study ID #: NL4724400013
• Secondary ID: 2013-005407-14
• Status: Completed
• Phase: Phase 1
• Start date: March 2015
• Est. completion date: November 2018

Study information

• Verified date: June 2019
• Source: Leiden University Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will test whether selected allogeneic bone marrow derived MSCs are safe by assessing the composite end point Biopsy Proven Acute Rejection (BPAR)/ graft loss at 12 months.

Description:

Kidney transplantation has improved survival and quality of life for patients with end-stage renal disease. However, despite advances in immunosuppressive therapy, long-term allograft survival outcomes have not improved over the last decade.

A promising novel therapeutic immunosuppressive option in the treatment of renal recipients with a profound effect on the fibrosis reaction is the clinical application of mesenchymal stromal cells (MSCs). Allogeneic MSCs offer the advantage of availability for clinical use without the delay required for expansion.

Although it is believed that allo MSCs are immune privileged, they could possibly elicit an anti-donor immune response, which may increase the incidence of rejection/ graft loss and impact the allograft survival on the long term. These safety issues should be studied before further studies are planned with allogeneic MSCs in the transplant setting.

MSCs are infused at a time point when immune suppression is lowered and the kidney is at increased risk for developing immune mediated injury. In addition, a large amount of the kidneys already has signs of fibrosis at this time point and MSCs might reduce the fibrosis which so importantly affects long term survival. MSCs will have no Human Leucocyte Antigen (HLA) sharing with the mismatches of the donor and the recipient should have no antibodies directed to the MSCs to reduce the anti-donor immune respons risk.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: November 2018
• Est. primary completion date: November 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Subject is willing to participate in the study, must be able to give informed consent and the consent must be obtained prior to any study procedure.

• Recipients of a first kidney graft from a living-unrelated or non-HLA identical living related donor.

• Panel Reactive Antibodies (PRA) = 50%.

• 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.

Exclusion Criteria:

• Double organ transplant recipient.

• Biopsy proven acute rejection (according to the Banff criteria) in the 4 weeks before MSC infusion.

• Patients with evidence of active infection or abscesses (with the exception of an uncomplicated urinary tract infection) before MSC infusion.

• Patients suffering from hepatic failure.

• Patients suffering from an active autoimmune disease.

• 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 tuberculosis according to current transplantation inclusion criteria.

• Subjects who currently an active opportunistic infection at the time of MSC infusion (e.g., herpes zoster [shingles], cytomegalovirus (CMV), Pneumocystis carinii (PCP), aspergillosis, histoplasmosis, or mycobacteria other than tuberculosis, BK) 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).

• Patients who are recipients of ABO incompatible transplants.

• Patients with severe total hypercholesterolemia (>7.5 mmol/L) or total hypertriglyceridemia (>5.6 mmol/L) (patients on lipid lowering treatment with controlled hyperlipidemia are acceptable).

Related Conditions & MeSH terms

• Graft Loss
• Rejection

Intervention

Drug:
• mesenchymal stromal cells
2 doses of 1-2x10^6 allogeneic bone marrow derives MSCs IV per/kg body weight at weeks 25 and 26 after transplantation

Locations

Country	Name	City	State
Netherlands	Leiden University 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	biopsy proven acute rejection / graft loss		12 months after transplantation
Secondary	Comparison of fibrosis by quantitative Sirius Red scoring		Before MSC infusion (week 24 after transplantation) and 6 months after MSC infusion (week 52 after transplantation)
Secondary	Serious adverse events		12 months after transplantation
Secondary	Renal function measured by cGFR (MDRD formula) and iohexol clearance		week 24 after transplantation (before MSC infusion) and 52 after transplantation
Secondary	CMV, BK infection (viremia, disease and syndrome; and subtypes of BK viremia) and other opportunistic infections		from baseline up to 26 weeks after MSC treatment
Secondary	Development of de novo donor specific antibodies (DSA) and immunological responses		at baseline, week 24 after transplantation (before MSC treatment) up to week 26 after MSC treatment