Source:http://linkedlifedata.com/resource/pubmed/id/19439014
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2009-5-14
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pubmed:abstractText |
We previously demonstrated that dendritic cells (DC) that have endocytosed apoptotic bodies of autologous leukemic cells (Apo-DC) can boost antileukemic T-cell responses. In this study, we report a description of the production procedure and product specification of the Apo-DC vaccine preparations for clinical use. Enriched populations of CD14+ monocytic precursors and CD19+ leukaemic cells were obtained using CliniMACS technology from a single leukapheresis product. Apoptotic bodies were obtained by irradiating (5 Gy) CD19+ selected B cells. DC were generated ex vivo by culturing monocytes with granulocyte macrophage colony-stimulating factor and interleukin-4. Following coculture with apoptotic bodies, DCs were matured with tumour necrosis factor-alpha. The mean percentage of CD14+ cells in the peripheral blood as well as in the leukapheresis product of the patients (n = 10) was approximately 2% (range, 0.8-3.3). Immunomagnetic selection using the CD14 reagent yielded a CD14+ population that was 91 +/- 2.2% (mean +/- SEM) pure. Immunomagnetic selection of CD19 expressing cells yielded a population that was 100 +/- 0.03% pure. Cell viability immediately after selection was 97% and 98% after 7 days of culture. The Apo-DC cellular vaccine product showed a mature phenotype, with a high rate of endocytosis (84%) of apoptotic leukemic B-cells. In conclusion, despite significant variability in the circulating monocyte frequency of the chronic lymphocytic leukaemia patients, our method permitted the production of a DC vaccine with high reproducibility and conforming with recommended quality standards.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1365-3083
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
69
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
529-36
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pubmed:meshHeading |
pubmed-meshheading:19439014-Aged,
pubmed-meshheading:19439014-Cancer Vaccines,
pubmed-meshheading:19439014-Dendritic Cells,
pubmed-meshheading:19439014-Female,
pubmed-meshheading:19439014-Flow Cytometry,
pubmed-meshheading:19439014-Humans,
pubmed-meshheading:19439014-Immunomagnetic Separation,
pubmed-meshheading:19439014-Leukapheresis,
pubmed-meshheading:19439014-Leukemia, Lymphocytic, Chronic, B-Cell,
pubmed-meshheading:19439014-Male
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pubmed:year |
2009
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pubmed:articleTitle |
Generation of a dendritic cell-based vaccine in chronic lymphocytic leukaemia using CliniMACS platform for large-scale production.
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pubmed:affiliation |
Immune and Gene Therapy Laboratory, Department of Oncology & Pathology, Cancer Centre Karolinska, Stockholm, Sweden.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, Non-U.S. Gov't
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