Infusion of T-Regulatory Cells in Kidney Transplant Recipients (The ONE Study)
Primary Purpose
Kidney Failure, Kidney Transplant
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
T Regulatory Cell Infusion
Sponsored by
About this trial
This is an interventional treatment trial for Kidney Failure, Kidney Transplant
Eligibility Criteria
Key Recipient Inclusion Criteria:
- Chronic renal insufficiency necessitating kidney transplantation
- Aged at least 18 years
- Donor is ABO (Blood type) compatible
Key Recipient Exclusion Criteria:
- HIV positive, EBV negative, or suffering from chronic viral hepatitis or tuberculosis
- Previously received any tissue or organ transplant other than planned kidney graft
- Genetically identical to the prospective organ donor at the HLA loci (0-0-0 mismatch)
- Panel Reactive Antibodies (PRA) >20%
- Concomitant malignancy or history of malignancy within 5 years prior to planned study entry (excluding successfully-treated non metastatic basal/squamous cell carcinoma of the skin)
- Ongoing treatment with systemic immunosuppressive drugs at study entry
Sites / Locations
- Massachusetts General Hospital
Outcomes
Primary Outcome Measures
Safety and Feasibility of T Regulatory Cell Infusion in Renal Transplantation
To examine in living donor renal transplant recipients the safety and feasibility of administering T regulatory cells derived from recipient PBMC stimulated with kidney donor PBMC in the presence of costimulatory blockade with belatacept.
Secondary Outcome Measures
T-Reg Measurements
To measure the presence, potency, and specificity of Treg in the peripheral circulation of kidney transplant recipients.
This will be done by in-vitro testing of the T-reg cell product and peripheral blood.
Reduction of Immunosuppression
To develop preliminary information on whether administration of the Treg cell product allows a tapering of conventional maintenance immunosuppression within 60 weeks after transplantation.
Full Information
NCT ID
NCT02091232
First Posted
March 13, 2014
Last Updated
November 15, 2021
Sponsor
Massachusetts General Hospital
Collaborators
Dana-Farber Cancer Institute, University of Regensburg
1. Study Identification
Unique Protocol Identification Number
NCT02091232
Brief Title
Infusion of T-Regulatory Cells in Kidney Transplant Recipients (The ONE Study)
Official Title
Renal Transplantation Followed By Infusion of T-Regulatory Cells Made With Belatacept Ex-Vivo
Study Type
Interventional
2. Study Status
Record Verification Date
November 2021
Overall Recruitment Status
Completed
Study Start Date
May 2014 (undefined)
Primary Completion Date
March 2, 2016 (Actual)
Study Completion Date
March 2, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital
Collaborators
Dana-Farber Cancer Institute, University of Regensburg
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This research study is for patients who are going to receive a kidney transplant from a living donor. After kidney transplantation, it is necessary for transplant recipients to take "immunosuppressive drugs". These drugs work by preventing the body's immune cells from attacking and "rejecting" the new kidney. Taking these drugs long-term may also cause harm to the transplanted kidney. Therefore, the transplant community is very interested in finding ways to decrease immunosuppressive drug treatment and further reduce the risk of kidney rejection. One method to do so is known as "induction of tolerance", which is when the person who receives a transplant has treatment to make their immune cells tolerant to the donor cells.
In this study, we will try to induce tolerance by mixing recipient cells and their donor's cells together with belatacept, an immunosuppressive drug. Belatacept is a protein that attaches to immune system cells, interferes with the immune response and results in tolerance induction.
After we mix the recipient cells with the donor's cells, we will sort out one particular kind of immune cell, called a regulatory T cell, and inject them back into the recipient. Regulatory T cells are the cells that are affected by induction to reduce rejection of donated organs. This method for inducing tolerance has been used in bone marrow transplantation, but this is the first time it is being done in kidney transplantation.
This study is being conducted as part of a unique collaboration of US and EU centers called The ONE Study. The ONE Study centers have agreed to work together using common protocols and procedures but with each testing their own regulatory population for safety and the ability to promote kidney survival. Sharing data among the participating sites will permit a deeper understanding of how and why some treatments might succeed while others work less well.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kidney Failure, Kidney Transplant
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
5 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Biological
Intervention Name(s)
T Regulatory Cell Infusion
Intervention Description
After blood is collected from the donor and recipient, the facility will sort out one particular kind of immune cell called a regulatory T cell which is strongly influenced by tolerance induction to minimize (suppress) responses to the donor cells. In this study, these regulatory T cells are the cells which will be given back to the recipient on Day 7 (+3 days) post-transplant.
Primary Outcome Measure Information:
Title
Safety and Feasibility of T Regulatory Cell Infusion in Renal Transplantation
Description
To examine in living donor renal transplant recipients the safety and feasibility of administering T regulatory cells derived from recipient PBMC stimulated with kidney donor PBMC in the presence of costimulatory blockade with belatacept.
Time Frame
2 Weeks
Secondary Outcome Measure Information:
Title
T-Reg Measurements
Description
To measure the presence, potency, and specificity of Treg in the peripheral circulation of kidney transplant recipients.
This will be done by in-vitro testing of the T-reg cell product and peripheral blood.
Time Frame
2 Years
Title
Reduction of Immunosuppression
Description
To develop preliminary information on whether administration of the Treg cell product allows a tapering of conventional maintenance immunosuppression within 60 weeks after transplantation.
Time Frame
60 Weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Key Recipient Inclusion Criteria:
Chronic renal insufficiency necessitating kidney transplantation
Aged at least 18 years
Donor is ABO (Blood type) compatible
Key Recipient Exclusion Criteria:
HIV positive, EBV negative, or suffering from chronic viral hepatitis or tuberculosis
Previously received any tissue or organ transplant other than planned kidney graft
Genetically identical to the prospective organ donor at the HLA loci (0-0-0 mismatch)
Panel Reactive Antibodies (PRA) >20%
Concomitant malignancy or history of malignancy within 5 years prior to planned study entry (excluding successfully-treated non metastatic basal/squamous cell carcinoma of the skin)
Ongoing treatment with systemic immunosuppressive drugs at study entry
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jim Markmann, MD PhD
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
32446407
Citation
Sawitzki B, Harden PN, Reinke P, Moreau A, Hutchinson JA, Game DS, Tang Q, Guinan EC, Battaglia M, Burlingham WJ, Roberts ISD, Streitz M, Josien R, Boger CA, Scotta C, Markmann JF, Hester JL, Juerchott K, Braudeau C, James B, Contreras-Ruiz L, van der Net JB, Bergler T, Caldara R, Petchey W, Edinger M, Dupas N, Kapinsky M, Mutzbauer I, Otto NM, Ollinger R, Hernandez-Fuentes MP, Issa F, Ahrens N, Meyenberg C, Karitzky S, Kunzendorf U, Knechtle SJ, Grinyo J, Morris PJ, Brent L, Bushell A, Turka LA, Bluestone JA, Lechler RI, Schlitt HJ, Cuturi MC, Schlickeiser S, Friend PJ, Miloud T, Scheffold A, Secchi A, Crisalli K, Kang SM, Hilton R, Banas B, Blancho G, Volk HD, Lombardi G, Wood KJ, Geissler EK. Regulatory cell therapy in kidney transplantation (The ONE Study): a harmonised design and analysis of seven non-randomised, single-arm, phase 1/2A trials. Lancet. 2020 May 23;395(10237):1627-1639. doi: 10.1016/S0140-6736(20)30167-7. Erratum In: Lancet. 2020 Jun 27;395(10242):1972.
Results Reference
derived
PubMed Identifier
26790369
Citation
Guinan EC, Cole GA, Wylie WH, Kelner RH, Janec KJ, Yuan H, Oppatt J, Brennan LL, Turka LA, Markmann J. Ex Vivo Costimulatory Blockade to Generate Regulatory T Cells From Patients Awaiting Kidney Transplantation. Am J Transplant. 2016 Jul;16(7):2187-95. doi: 10.1111/ajt.13725. Epub 2016 Mar 11.
Results Reference
derived
Links:
URL
http://www.onestudy.org/
Description
Related Info
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Infusion of T-Regulatory Cells in Kidney Transplant Recipients (The ONE Study)
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