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PŘÍPRAVA MYELOM-SPECIFICKÝCH T LYMFOCYTŮ AKTIVOVANÝCH DENDRITICKÝMI BUŇKAMI NALOŽENÝMI NONAPEPTIDY ODVOZENÝMI OD MUCINOVÉHO PROTEINU MUC1 A KATALYTICKÉ PODJEDNOTKY TELOMERÁZY hTERT
Title in English | THE PREPARATION OF MYELOMA-SPECIFIC T CELLS ACTIVATED WITH DENDRITIC CELLS LOADED WITH NONAPEPTIDES DERIVED FROM MUCIN PROTEIN MUC1 AND CATALYTIC SUBUNIT OF TELOMERASE hTERT |
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Authors | |
Year of publication | 2008 |
Type | Article in Periodical |
Magazine / Source | Klinická onkologie |
MU Faculty or unit | |
Citation | |
Field | Oncology and hematology |
Keywords | Multiple myeloma; immunotherapy; interferon gamma; hTERT; MUC1 |
Description | Backgrounds: Multiple myeloma is an incurable hematological disease. High-dose chemotherapy including autologous stem cell transplantation is recently considered a standard therapy for myeloma. Unfortunately, a relapse of the disease is inevitable. Therefore, new approaches such as immunotherapy have been considered recently. A specific activation of cytotoxic T cells can be reached using dendritic cells loaded with tumor-specific antigens. The HLA-A2-specific nonapeptides as hTERT derived from catalytic subunit of telomerase and MUC1 derived from mucin protein can be used. Design and subjects: Activation, identification, separation and expansion of myeloma-specific T cells from healthy HLA-A2 blood donors were tested in an in vitro study using hTERT and MUC1 nonapeptides as tumor-specific antigens. Methods and results: T cells and dendritic cells were obtained from peripheral blood. T cells were repeatedly stimulated with hTERT and MUC1 nonapeptide-loaded dendritic cells. Activated myeloma-specific T cells produced interferon gamma and were evaluated by flow cytometry. The activated T cells were immunomagnetically separated and in vitro expanded to the number usable in clinical trials. Conclusions: This study demonstrates feasibility of a specific activation, identification, separation and expansion of tumor-specific T cells that can be used in myeloma therapy. |
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