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CD45RA Depleted T-cell Infusion for Prevention of Infections After TCRab/CD19-depleted Allo-HSCT

F

Federal Research Institute of Pediatric Hematology, Oncology and Immunology

Status and phase

Completed
Phase 3
Phase 2

Conditions

Graft-versus-Host Disease
Opportunistic Infections
GvHD
Lymphoma
Leukemia
Myelodysplastic Syndromes

Treatments

Biological: CD45RA-depleted peripheral blood mononuclear cells

Study type

Interventional

Funder types

Other

Identifiers

NCT02942173
CD45RAndom_2016_1

Details and patient eligibility

About

The purpose of this prospective randomized study is to determine whether infusions of T-memory cells prevent infections in children with leukemia after allogeneic alpha, beta T-cell receptor (TcRab)/CD19-depleted hematopoietic stem cell transplantation (HSCT).

Full description

Graft-versus-host disease (GVHD) remains the most important direct complication of hematopoietic stem cell transplantation. Methods used to prevent GVHD include diverse pharmacologic interventions and ex vivo methods of T-cell depletion, the latter being the most effective ones. Historically depletion of T-cells from the graft is associated with increased rate of graft failure, relapse of malignant disease and prolonged immune deficiency. Selective depletion of TCR-alpha/beta T-lymphocytes is a new method of hematopoietic stem cell graft manipulation, which is thought to conserve important cell populations, e.g. NK cells and gamma/delta T cells within the graft. Preliminary results suggest that TCR alpha/beta depletion ensures high engraftment rate, low early mortality and good control of GVHD. The problem of delayed immune reconstitution and life-threatening viral infections remains incompletely resolved.

Depletion of naive (CD45RA-positive) T-cells was developed as a new method of graft manipulation to prevent GVHD. Research data indicate that alloreactivity is associated mainly with naive T-cell fraction. In vitro depletion of CD45RA lowers significantly the alloreactive response while retaining reactivity to pathogens.

In previous pilot protocol the investigators confirmed that infusion after TCR-alpha/beta depleted transplantation of low doses of CD45RA-depleted mononuclear cells are safe and potentially protective against viral infections. The biologic readout for the protocol was a quantitative assessment of T-cell reactivity to common pathogens after infusion and owing to the trial results expansion of CMV-specific CD8 T-cells was discovered in most of the patients.

In current randomized protocol the investigators are posing a question if donor lymphocytes infusion (DLI) of low doses of CD45RA-depleted mononuclear cells are effective in viral prophylaxis after TCR-alpha/beta depleted transplantation.

Enrollment

150 patients

Sex

All

Ages

Under 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who are considered candidates for allogeneic hematopoietic stem cell transplantation and have one of the following diagnoses:

    • Acute lymphocytic leukemia (ALL)
    • Acute myeloid leukemia
    • Acute biphenotypic leukemia
    • Acute bilinear leukemia
    • Lymphoma
    • Myelodysplastic syndrome
    • Chronic myeloid leukemia
  • Transplant processing: TCR ab/CD19-depletion

  • Donors:

    • HLA-match unrelated volunteers
    • Partly and haploidentical relative

Exclusion criteria

  • ALL patients not in remission
  • Patients with uncontrolled infections
  • Clearance of creatinine < 70 ml/min
  • Cardiac ejection fraction < 40%
  • Patients who can perform pulmonary function tests will be excluded if they have a diffusing capacity of the lung for carbon monoxide (DLCO) (corrected for hemoglobin) of < 50% predicted; patients who are unable to perform pulmonary function tests will be excluded if the oxygen (O2) saturation is < 92% on room air
  • Patients who have liver function test (LFTs) (including total bilirubin, aspartate aminotransferase [AST] and alanine aminotransferase [ALT]) >= twice the upper limit of normal
  • Mental disease of both patient, patient's tutor (if patient is under age 18) and donor, that hinder understanding of main point of the study and keeping treatment plan, hygiene and sanitation

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

150 participants in 2 patient groups

CD45RA-
No Intervention group
CD45RA+
Experimental group
Treatment:
Biological: CD45RA-depleted peripheral blood mononuclear cells

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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