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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).
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| CD45RA- | No Intervention | ||
| CD45RA+ | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| CD45RA-depleted peripheral blood mononuclear cells | Biological | Infusion of escalating doses of CD45RA-depleted donor-derived allogeneic peripheral blood mononuclear cells |
|
| Measure | Description | Time Frame |
|---|---|---|
| cumulative incidence of the probability of CMV-reactivation after HSCT | 120 days after HSCT | |
| cumulative incidence of acute GVHD grade II-IV. | 150 days after HSCT |
| Measure | Description | Time Frame |
|---|---|---|
| cumulative incidence of of CMV-disease at 100,180 and 365 days after HSCT | 100, 180 and 365 days after HSCT | |
| overall survival at 365 days after HSCT | 365 days after HSCT | |
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Inclusion Criteria:
Patients who are considered candidates for allogeneic hematopoietic stem cell transplantation and have one of the following diagnoses:
Transplant processing: TCR ab/CD19-depletion
Donors:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Michael Maschan, PhD | Fedaral Research Center for pediatric hematology, oncology and immunology | Study Director |
| Larisa Shelikhova, PhD | Fedaral Research Center for pediatric hematology, oncology and immunology | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Federal Research Center for pediatric hematology, oncology and immunology | Moscow | 117997 | Russia |
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| Event-free survival at 365 days after HSCT |
| 365 days after HSCT |
| cumulative incidence of relapse at 6 months and 365 days after HSCT | 6 months and 365 days |
| cumulative incidence of transplant-related mortality at 6 months after HSCT | 6 months |
| cumulative incidence of chronic GvHD | 1 year after HSCT |
| cumulative incidence of neutrophil and platelets engraftment at 14 and 30 days after HSCT | 14 and 30 days |
| ID | Term |
|---|---|
| D007938 | Leukemia |
| D008223 | Lymphoma |
| D009190 | Myelodysplastic Syndromes |
| D009894 | Opportunistic Infections |
| D006086 | Graft vs Host Disease |
| ID | Term |
|---|---|
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D008232 | Lymphoproliferative Disorders |
| D008206 | Lymphatic Diseases |
| D007160 | Immunoproliferative Disorders |
| D007154 | Immune System Diseases |
| D001855 | Bone Marrow Diseases |
| D007239 | Infections |
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