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The immune system has offensive and defensive capacities. In bone marrow transplantation, offensive cells in the donor grafts may attack host's organs, leading to a complication known as Graft versus Host Disease (GVDH). At present, patients receive steroid treatment to combat this tricky situation. Nevertheless, some patients do not respond to this therapy. Recently, it has been shown that immune system cells having defensive capacities can help in preventing the occurrence of a GVDH.
This study aims to evaluate if these protective cells together with a non-standard immunosuppressor can improve the clinical condition and suppress the activity of the offensive cells in the graft.
Full description
TREATMENT PLAN
1 Immunosuppressive drugs (DTI and control arms)
Rapa will be started within 2 weeks after inclusion. Rapa will be given at 2-6 mg loading dose for one day, followed by approximately 1mg daily to achieve a target trough level of 5 to 10 ng/mL. The frequency of trough level measurements will be done according to the investigator choice;
Rapa may be discontinued in case of resolution of chronic GVHD ≥ 3 months or in case of un-manageable side effects or progression of chronic GVHD.
Calcineurin inhibitor discontinuation within 2 weeks after rapa initiation. No other modification of immunosuppressive drugs and in particular no decrease in the dose of steroids (unless necessary for side effects).
Evaluation of chronic GVHD 60 days after rapa initiation. DTI will not be given in patients who had progression of their GVHD on day 60 nor in those who are in CR of their GVHD.
Apheresis of the donor will be performed 60-90 days after first day of rapa administration to the patient.There will be no particular preparation of the donor prior to leukapheresis. After written informed consent, the donor will undergo leukaphereses on 1 day. Leukapheresis will be performed using a continuous flow blood cell separator and following a mononuclear cell collection protocol. The volume of blood processed will be 20 liters. Anticoagulation will be performed with the ACD-A / heparin solution.
Treg will be isolated at the LTCG of the CHU of Liège from apheresis product with the CliniMACS separation system (MiltenyiBiotec) following a two-step procedure (CD8 and CD19 depletion followed by CD25 positive selection)according to the manufacturer's recommendation. Aliquots (≈ 3 mL) of the Treg product will be saved for analyses.
Treg will be infused i.v.60-90 days after first day of rapa administration and after calcineurin inhibitor discontinuation. No DTI will be performed in the control arm.
Low-dose Il-2 (1x106 IU/day) will be started the day of DTI and will be continued for a period of 2months in order to expand infused donor Tregs.
PATIENTS' FOLLOW-UP
Quality controls of cell products 1.1 Peripheral blood.
The following laboratory analyses will be performed in the peripheral blood of the donor on the days of lymphocyte collections :
1.1.2 Leukapheresis product as well as start, intermediate, and final fractions of Treg selection.
The following laboratory analyses will be performed in the lymphocyte collection as well as start, intermediate and final fractions of the Treg selection:
• Nucleated cell count and differential on an automated cell counter;
1.1.3Release criteria.
The following criteria should be met for release:
• ≥ 0.5 x106 cells/kg recipient;
Toxicities of cell infusions Potential toxicities associated with Treg infusions will be carefully monitored per standard procedures.
Clinical data
Patient will be carefully observed and the following clinical parameters will be recorded:
• Incidence, timing and severity of acute GVHD following DTI, its treatment and outcome;
Immunological data(performed in the GIGA at the ULG for all but the analyses of methylation status of CpG dinucleotides located in a conserved region of FoxP3 intron 1 that will be performed at the UCL).
Immune recovery I (flow cytometry). The following analyses will be performed (starting with 5 mL of blood).
Immune recovery II. Isolation of T-cell subsets for analyses of repertoire diversity through next-generation sequencing (NGS; starting from 50 mL of blood). The following subsets will be isolated (~50,000 cells each) and then cryopreserved:
Enrollment
Sex
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Volunteers
Inclusion and exclusion criteria
Signed informed consent.
Grafts from HLA-identical siblings or HLA-matched unrelated donor (1 of 10 HLA-mismatch is allowed).
≥ 18 years of age.
Steroid-refractory or steroid-resistant chronic GVHD defined as:
or severe chronic GVHD and contra-indication to the use of steroids and at least failed one prior line of treatment.
Severe chronic GVHD according to NIH definition.
No prior failure of rapamycine as treatment for chronic GVHD
No contra-indication to the use of rapamycin.
No alemtuzumab administration in the last 6 months.
GFR > 25 mL/min.
No HIV seropositivity.
No fungal infection with radiological progression after treatment with amphotericine B or active azoles for > 1 month.
No other uncontrolled infection.
No progression of the hematological malignancy.
Karnofsky performance score ≥ 70%.
DLCO > 35% and no need of supplemental continuous oxygen.
No active post-transplant microangiopathy and no previous microangiopathy while on rapamycine.
No uncontrolled hypertriglyceridemia.
2 Donor criteria : DTI arm only.
Donor ≥ 18 years of age.
Written informed consent to perform apheresis from the donor (all patients) and permission from the third party donor registry (in case of unrelated donor).
Standard criteria for leukapheresis and DLI following complete work-up according to standard procedures.
Primary purpose
Allocation
Interventional model
Masking
19 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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