BÜCHLER, Tomáš, Roman HÁJEK, Ludmila BOURKOVÁ, Lucie KOVÁŘOVÁ, Romana MUSILOVÁ, Alena BULIKOVÁ, M. DOUBEK, A. SVOBODNÍK, Iveta MARESCHOVÁ, Pavlína VÁŇOVÁ, Eva TŮZOVÁ, Petra VIDLÁKOVÁ, Jiří VORLÍČEK and Miroslav PENKA. Generation of antigen-loaded dendritic cells in a serum-free medium using different cytokine combinations. Vaccine. 2003, neuveden, 2/2003, p. 877-882. ISSN 0264-410X.
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Basic information
Original name Generation of antigen-loaded dendritic cells in a serum-free medium using different cytokine combinations.
Authors BÜCHLER, Tomáš (703 Slovakia), Roman HÁJEK (203 Czech Republic, guarantor), Ludmila BOURKOVÁ (203 Czech Republic), Lucie KOVÁŘOVÁ (203 Czech Republic), Romana MUSILOVÁ (203 Czech Republic), Alena BULIKOVÁ (203 Czech Republic), M. DOUBEK (203 Czech Republic), A. SVOBODNÍK (203 Czech Republic), Iveta MARESCHOVÁ (203 Czech Republic), Pavlína VÁŇOVÁ (203 Czech Republic), Eva TŮZOVÁ (203 Czech Republic), Petra VIDLÁKOVÁ (203 Czech Republic), Jiří VORLÍČEK (203 Czech Republic) and Miroslav PENKA (203 Czech Republic).
Edition Vaccine, 2003, 0264-410X.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30200 3.2 Clinical medicine
Country of publisher Netherlands
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 3.007
RIV identification code RIV/00216224:14110/03:00008552
Organization unit Faculty of Medicine
Keywords in English dendritic cells; in vitro cell culture; cytokines; immunotherapy
Tags cytokines, dendritic cells, Immunotherapy, in vitro cell culture
Changed by Changed by: Jana Mamulová, učo 71312. Changed: 21/5/2003 07:30.
Abstract
Dendritic cells (DCs) are antigen-presenting cells that play a critical role in the induction of cytotoxic T-lymphocytes. An optimal method for the generation of DC for clinical use remains to be established. The aim of our study was to find an optimal cytokine combination for DC generation from peripheral blood stem cells (PBSC) and peripheral blood mononuclear cells (PBMC) in serum-free conditions. Serial immunophenotyping enabled us to observe changes in DC content during the culture as well as the development of maturation and activation markers. As a source for DC culture, we used PBSC from patients with multiple myeloma after stem cell mobilization using cyclophosphamide and G-CSF, or PBMC from healthy donors without mobilization. The cells were cultured in a serum-free medium with different cytokine combinations including GM-CSF, TNF-[alpha], Flt-3, CD40L, IFN-[gamma], IL-1[alpha], IL-6, PGE1, and IL-4. The cell cultures were evaluated by immunophenotyping. For PBMC, interleukin-12 assay was performed. For PBSC, the yield of DC as determined by CD83+ cell count ranged from 0.6 x 105 to 30.1 x 104 (mean: 9.4 x 104) of DC generated per 1 x 106 of initially plated nucleated cells from apheresis. This yield corresponded to (0.3-19.1) x 105 (mean: 4.3 x 105) per 1 x 106 of CD34+ cells in the apheresis products. For PBMC, the yield was (0.4-24.8) x 104 (mean: 2.4 x 104) of DC generated per 1 x 106 of initially plated mononuclear cells from venous blood. The cultured cells expressed the mature immunophenotype. No significant differences in cell yield or immunophenotype were detected when comparing different cytokine combinations. (C) 2002 Elsevier Science Ltd. All rights reserved.
Links
MSM 141100003, plan (intention)Name: Zevní prostředí - karcinogeneze - onkologie
Investor: Ministry of Education, Youth and Sports of the CR, Environment - carcinogenesis - oncology
NC6152, research and development projectName: Hodnocení léčebného efektu dentrických buněk u nemocných s mnohočetným myelomem.
Investor: Ministry of Health of the CR, Evaluation of dentritic cells administration in multiple myeloma.
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