Inclusion Criteria:

        Acute leukemia and MDS patients with molecular or cytogenetic relapse in peripheral blood
        (PB) or bone marrow (BM) samples obtained during monitoring for relapse after allogeneic
        SCT.

        MRD detected by Ig/TCR gene rearrangement testing or any detected disease specific DNA or
        RNA sequence or disease specific cell surface Proteins or mixed recipient chimerism (MC) ≥
        1% and < 40%, or levels ≥ 10-4 of BCR-ABL/ABL ratio or any other disease specific
        cytogenetic abnormality will trigger CIK cell interventions.

          -  Respecting MC, MC = 1% of autologous/recipient signals in PB samples must be confirmed
             by another PB or BM sample within one week. Patients with MC = 1% of
             autologous/recipient signals in CD33+ and/or CD34+ subpopulations in PB samples must
             be confirmed by BM analyses within one week. Acute leukemia and MDS patients with MC =
             1% of autologous/recipient signals including signals in CD33+ and/or CD34+
             subpopulations in BM samples must not be confirmed.

          -  Acute leukemia and MDS patients with frank relapse ≥ 120 days after allogeneic SCT who
             achieved complete remission (CR) or blast clearance (i.e. <5% blasts) in the bone
             marrow after re-induction chemotherapy.

          -  All patients must be in complete remission or have achieved blast clearance (i.e. <5%
             blasts) in the bone marrow before 1st CIK cell treatment (bone marrow assessment at a
             maximum of 7 days in advance of 1st treatment is obligatory).

          -  Patients without immunosuppressive agents and steroids for at least 7 days.

          -  Patients without chemo- or immune therapy during CIK cell treatment, except patients
             with thyrosine-kinase inhibitors (TKI) for treatment of BCR-ABL positive leukemia.
             Last DLI treatment must be 4 weeks before 1st CIK cell treatment.

          -  Patients with < grade II aGvHD.

          -  Patients with Karnowsky or Lansky performance status ≥ 50%.

          -  Patients and/or his/her legal representative having reviewed the patient
             information/informed consent form and have had their questions answered and have given
             written informed consent.

        Exclusion Criteria:

          -  Acute leukemia and MDS patients with hematologic relapse < day 120 after allogeneic
             stem cell transplantation.

          -  Patients with 5% and more malignant cells in a representative bone marrow analysis
             performed at a maximum of 7 days before 1st CIK cell treatment (obligatory).

          -  Patients with immunosuppressive agents or steroids.

          -  Patients with chemo- or immune therapy, except patients with thyrosine-kinase
             inhibitors (TKI) for BCR-ABL positive leukemias.

          -  Patients with ≥ grade II GvHD.

          -  Patients with rapid T cell regeneration and any signs of GvHD

          -  Patients with Karnowsky or Lansky performance status < 50%.

          -  Patients and/or his/her legal representative having reviewed the patient
             information/informed consent form and have had their questions answered and have not
             given written informed consent.

          -  HIV-positive patients.

          -  HBV/HCV positive patients.

          -  Patients with prior solid organ transplantation.

          -  Patients treated with any other investigational product within the last 28 days or
             five half-lives (whichever is longer).

          -  Hypersensitivity to any component of the study drug

          -  Female patients of child-bearing potential not agreeing to use a highly effective
             method of birth control resulting in a low failure rate (i.e. < 1%) when used
             consistently and correctly.

          -  Male patients with female partners of childbearing potential not agreeing to use a
             highly effective method birth control resulting in a low failure rate (i.e. < 1%) when
             used consistently and correctly.

          -  Pregnancy/Breastfeeding.

          -  Patients with severe infections or signs/symptoms of infection within 2 weeks prior to
             study start.