Abstract
The capacity to generate effective dendritic cells (DC) from adult acute lymphoblastic leukemia (ALL) patients in complete remission (CR) and off-therapy was investigated. Monocyte-derived DC cultured in the presence of granulocyte-macrophage colony-stimulating factor, interleukin (IL)-4 and tumor necrosis factor (TNF)-alpha expressed maturation markers, produced IL-12 and loaded apoptotic bodies to a similar extent to normal DC. Patients' circulating T and NK lymphocytes were normally represented and, after stimulation, were capable of producing TNF-alpha and interferon-gamma to a similar extent to control lymphocytes. DC loaded with leukemia-derived apoptotic bodies increased their ability to stimulate both allogeneic and autologous lymphocytes, and to generate specific anti-leukemic CD3 + cells. These findings offer a rationale for the design of DC-based vaccine programs for adult ALL patients in CR with the aim of controlling/eradicating the disease.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Aged
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Apoptosis*
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Cancer Vaccines / therapeutic use
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Cell Proliferation
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Dendritic Cells / immunology*
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Female
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Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
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Humans
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Immunophenotyping
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Interferon-gamma / metabolism
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Interleukin-12 / metabolism
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Interleukin-4 / pharmacology
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Killer Cells, Natural / immunology
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Male
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Middle Aged
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Phagocytosis
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Precursor Cell Lymphoblastic Leukemia-Lymphoma / immunology*
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Precursor Cell Lymphoblastic Leukemia-Lymphoma / pathology
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Precursor Cell Lymphoblastic Leukemia-Lymphoma / prevention & control*
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Remission Induction
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T-Lymphocytes / immunology
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T-Lymphocytes / metabolism
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T-Lymphocytes / pathology
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T-Lymphocytes, Cytotoxic / immunology
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Tumor Cells, Cultured
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Tumor Necrosis Factor-alpha / pharmacology
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Vaccination*
Substances
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Cancer Vaccines
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Tumor Necrosis Factor-alpha
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Interleukin-12
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Interleukin-4
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Interferon-gamma
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Granulocyte-Macrophage Colony-Stimulating Factor