Clinical and immunologic outcomes following haplocompatible donor lymphocyte infusions

We retrospectively analyzed the characteristics of 16 consecutive pediatric patients who received one or more G-CSF-mobilized donor lymphocyte infusions (DLI) following a T-cell-depleted haplocompatible hematopoietic SCT (HSCT) to enhance immune recovery and/or treat an infection. The median time fr...

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Veröffentlicht in:Bone marrow transplantation (Basingstoke) 2009-12, Vol.44 (12), p.805-812
Hauptverfasser: Dvorak, C C, Gilman, A L, Horn, B, Jaroscak, J, Dunn, E A, Baxter-Lowe, L A, Cowan, M J
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container_end_page 812
container_issue 12
container_start_page 805
container_title Bone marrow transplantation (Basingstoke)
container_volume 44
creator Dvorak, C C
Gilman, A L
Horn, B
Jaroscak, J
Dunn, E A
Baxter-Lowe, L A
Cowan, M J
description We retrospectively analyzed the characteristics of 16 consecutive pediatric patients who received one or more G-CSF-mobilized donor lymphocyte infusions (DLI) following a T-cell-depleted haplocompatible hematopoietic SCT (HSCT) to enhance immune recovery and/or treat an infection. The median time from HSCT to administration of first DLI was 12 weeks and the median dose of DLI administered was 3 × 10 4 /kg (range, 2.5–6 × 10 4 /kg). The incidence of Grade I–II acute GVHD was 19% (95% confidence interval (CI), 6–44%), and there were no cases of Grade III–IV acute GVHD. Chronic GVHD developed in 13% (95% CI, 2–37%) of patients. In surviving patients who did not undergo a second stem cell infusion, T-cell numbers and function increased to a protective level in a median of 3 months (range, 2–12.5 months) following the first DLI administration. In patients given DLI for treatment of an infection, 75% (95% CI, 46–92%) cleared their infection after a median of 9 weeks (range, 1–27 weeks). In patients with CMV infection, the development of CMV-specific T cells was observed following DLI. The 1-year overall survival following haplocompatible DLI was 71% (95% CI, 59–83%), with a median follow-up of 16 months from the first DLI.
doi_str_mv 10.1038/bmt.2009.87
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The median time from HSCT to administration of first DLI was 12 weeks and the median dose of DLI administered was 3 × 10 4 /kg (range, 2.5–6 × 10 4 /kg). The incidence of Grade I–II acute GVHD was 19% (95% confidence interval (CI), 6–44%), and there were no cases of Grade III–IV acute GVHD. Chronic GVHD developed in 13% (95% CI, 2–37%) of patients. In surviving patients who did not undergo a second stem cell infusion, T-cell numbers and function increased to a protective level in a median of 3 months (range, 2–12.5 months) following the first DLI administration. In patients given DLI for treatment of an infection, 75% (95% CI, 46–92%) cleared their infection after a median of 9 weeks (range, 1–27 weeks). In patients with CMV infection, the development of CMV-specific T cells was observed following DLI. 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Graft versus host reaction ; Cell Biology ; Child ; Child, Preschool ; Chronic Disease ; Confidence intervals ; Cytomegalovirus ; Cytomegalovirus - immunology ; Cytomegalovirus Infections - immunology ; Cytomegalovirus Infections - mortality ; Disease-Free Survival ; Female ; Graft vs Host Disease - blood ; Graft vs Host Disease - immunology ; Graft vs Host Disease - mortality ; Graft-versus-host reaction ; Granulocyte colony-stimulating factor ; Haplotypes ; Health aspects ; Hematologic Neoplasms - blood ; Hematologic Neoplasms - immunology ; Hematologic Neoplasms - mortality ; Hematologic Neoplasms - therapy ; Hematology ; Hematopoietic Stem Cell Transplantation ; Hematopoietic stem cells ; Humans ; Immune response ; Infant ; Infection ; Infections ; Internal Medicine ; Lymphocyte Transfusion ; Lymphocytes ; Lymphocytes T ; Male ; Medical sciences ; Medicine ; Medicine &amp; Public Health ; original-article ; Patients ; Pediatrics ; Physiological aspects ; Prevention ; Public Health ; Recovery of Function - immunology ; Retrospective Studies ; Risk factors ; Severe Combined Immunodeficiency - blood ; Severe Combined Immunodeficiency - immunology ; Severe Combined Immunodeficiency - mortality ; Severe Combined Immunodeficiency - therapy ; Stem cell transplantation ; Stem Cells ; Survival Rate ; Time Factors ; Transfusions. 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Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Blood Donors</topic><topic>Bone marrow, stem cells transplantation. Graft versus host reaction</topic><topic>Cell Biology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Chronic Disease</topic><topic>Confidence intervals</topic><topic>Cytomegalovirus</topic><topic>Cytomegalovirus - immunology</topic><topic>Cytomegalovirus Infections - immunology</topic><topic>Cytomegalovirus Infections - mortality</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Graft vs Host Disease - blood</topic><topic>Graft vs Host Disease - immunology</topic><topic>Graft vs Host Disease - mortality</topic><topic>Graft-versus-host reaction</topic><topic>Granulocyte colony-stimulating factor</topic><topic>Haplotypes</topic><topic>Health aspects</topic><topic>Hematologic Neoplasms - blood</topic><topic>Hematologic Neoplasms - immunology</topic><topic>Hematologic Neoplasms - mortality</topic><topic>Hematologic Neoplasms - therapy</topic><topic>Hematology</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Hematopoietic stem cells</topic><topic>Humans</topic><topic>Immune response</topic><topic>Infant</topic><topic>Infection</topic><topic>Infections</topic><topic>Internal Medicine</topic><topic>Lymphocyte Transfusion</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>original-article</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Physiological aspects</topic><topic>Prevention</topic><topic>Public Health</topic><topic>Recovery of Function - immunology</topic><topic>Retrospective Studies</topic><topic>Risk factors</topic><topic>Severe Combined Immunodeficiency - blood</topic><topic>Severe Combined Immunodeficiency - immunology</topic><topic>Severe Combined Immunodeficiency - mortality</topic><topic>Severe Combined Immunodeficiency - therapy</topic><topic>Stem cell transplantation</topic><topic>Stem Cells</topic><topic>Survival Rate</topic><topic>Time Factors</topic><topic>Transfusions. 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subjects Acute Disease
Adolescent
Adult
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Biological and medical sciences
Blood Donors
Bone marrow, stem cells transplantation. Graft versus host reaction
Cell Biology
Child
Child, Preschool
Chronic Disease
Confidence intervals
Cytomegalovirus
Cytomegalovirus - immunology
Cytomegalovirus Infections - immunology
Cytomegalovirus Infections - mortality
Disease-Free Survival
Female
Graft vs Host Disease - blood
Graft vs Host Disease - immunology
Graft vs Host Disease - mortality
Graft-versus-host reaction
Granulocyte colony-stimulating factor
Haplotypes
Health aspects
Hematologic Neoplasms - blood
Hematologic Neoplasms - immunology
Hematologic Neoplasms - mortality
Hematologic Neoplasms - therapy
Hematology
Hematopoietic Stem Cell Transplantation
Hematopoietic stem cells
Humans
Immune response
Infant
Infection
Infections
Internal Medicine
Lymphocyte Transfusion
Lymphocytes
Lymphocytes T
Male
Medical sciences
Medicine
Medicine & Public Health
original-article
Patients
Pediatrics
Physiological aspects
Prevention
Public Health
Recovery of Function - immunology
Retrospective Studies
Risk factors
Severe Combined Immunodeficiency - blood
Severe Combined Immunodeficiency - immunology
Severe Combined Immunodeficiency - mortality
Severe Combined Immunodeficiency - therapy
Stem cell transplantation
Stem Cells
Survival Rate
Time Factors
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
Transplantation
Transplantation, Homologous
title Clinical and immunologic outcomes following haplocompatible donor lymphocyte infusions
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