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

Last updated: March 15, 2023
Sponsor: Federal Research Institute of Pediatric Hematology, Oncology and Immunology
Overall Status: Completed

Phase

2/3

Condition

Leukemia

Lymphoma

Aids And Aids Related Infections

Treatment

N/A

Clinical Study ID

NCT02942173
CD45RAndom_2016_1
  • Ages < 25
  • All Genders

Study Summary

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).

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients who are considered candidates for allogeneic hematopoietic stem celltransplantation 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

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 adiffusing capacity of the lung for carbon monoxide (DLCO) (corrected for hemoglobin)of < 50% predicted; patients who are unable to perform pulmonary function tests willbe excluded if the oxygen (O2) saturation is < 92% on room air
  • Patients who have liver function test (LFTs) (including total bilirubin, aspartateaminotransferase [AST] and alanine aminotransferase [ALT]) >= twice the upper limit ofnormal
  • Mental disease of both patient, patient's tutor (if patient is under age 18) anddonor, that hinder understanding of main point of the study and keeping treatmentplan, hygiene and sanitation

Study Design

Total Participants: 150
Study Start date:
October 01, 2016
Estimated Completion Date:
August 21, 2020

Study 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.

Connect with a study center

  • Federal Research Center for pediatric hematology, oncology and immunology

    Moscow, 117997
    Russian Federation

    Site Not Available

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