Eight-Treg Study:Trial of Adoptive Immunotherapy With Autologous ex Vivo Expanded Regulatory CD8+ T Cells in Living Donor Kidney Transplant Recipients

Inclusion Criteria:

1. WOCBP must have a negative serum pregnancy test.

2. Respects the following conditions:

   • Condition 1: number of CD8+ Tregs / ml of blood > 2.096x106 CD8+ Tregs / weight

   • Condition 2 (depending on the dose level considered):

     • Dose 1: number of CD8+ Tregs / ml of blood > 1.15x104 CD8+ Tregs + 3.18x103 CD8+ Tregs / weight
     • Dose 2: number of CD8+ Tregs / ml of blood > 4.6x104 CD8+ Tregs + 3.18x103 CD8+ Tregs / weight
     • Dose 3: number of CD8+ Tregs / ml of blood > 9.22x104 CD8+ Tregs + 3.18x103 CD8+ Tregs / weight

Pre-Exclusion Criteria:

1. Patient has previously received any tissue or organ transplant other than the planned kidney graft.
2. Genetically identical to the prospective organ donor at the HLA loci.
3. Known contraindication to the protocol-specified treatments / medications or components used in the manufacture of the experimental drug.
4. Presence of donor-specific antibodies (DSA) detected prior transplantation determined by Luminex within 3 months or presence of cytotoxic DSA determined by cell-based CDC assay.
5. Previous treatment with any desensitisation procedure (with or without IVIg).
6. 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).
7. ABO incompatibility
8. Evidence of significant local or systemic infection on visit 1.
9. Malignant or pre-malignant haematological conditions.
10. Ongoing treatment with systemic IS drugs at visit 1 (except corticoids \< 10 mg).
11. Any vaccine (or vaccine recall) dated within 3 months on visit 1 except the SARS Cov2*.
12. Participation in another clinical trial during the study or within 28 days prior to the planned study entry and / or exposure to an investigational product during the study or within 28 days prior to the planned study entry (date of signature of the consent collection form).
13. Women who are pregnant (or planning to be during the course of the study) or breastfeeding or women with a positive pregnancy test on enrolment (visit 1, screening failure).
14. Psychological, familial, sociological or geographical factors that potentially hampering compliance with the study protocol and follow-up visit schedule.
15. Any form of drug abuse, psychiatric disorder, or other condition that, in the opinion of the investigator, may invalidate communication with the investigator and/or designated study personnel.
16. Any pro-coagulant disposition, as evidences by a past history of thromboembolic disease or abnormal laboratory coagulation parameters which, in the judgement of the investigator, would place the subject at undue risk.
17. Any condition resulting in a substantial reduction in the volume of the pulmonary vasculature or an increase in the pulmonary vascular resistance. Any disease or disease process leading to substantially elevated pulmonary arterial pressure (as evidences by electrocardiography, echocardiography, radiology or cardiac catheterization) or right heart hypertrophy or dysfunction.
18. Known atrial or ventricular septal defects posing a risk of paradoxical embolism of infused cells or cell aggregates.
19. Patients unable to freely give their informed consent (e.g. patients under guardianship, curatorship, protection of justice).
20. Patients deprived of their liberty.

Exclusion Criteria:

1. Human Immunodeficiency Virus (HIV)-positive, Epstein-Barr Virus (EBV)-negative (if donor is EBV positive), HTLV positive, syphilis-positive serology or suffer from chronic viral hepatitis.
2. Significant liver disease, defined as persistently elevated Aspartate Transaminase (AST) and / or Alanine Transaminase (ALT) levels > 2 x upper limit of normal range.

Donor:

Pre-Inclusion Criteria:

1. Willing and able to provide a blood and an urine sample for the immune monitoring.
2. Willing to provide personal and medical/biological data for the trial analysis.
3. Signed and dated written informed consent *.
4. Aged at least of 18 years the day the consent is signed.
5. Affiliated or beneficiary of a social security scheme.
6. Speaking and understanding French.