rdf:type |
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lifeskim:mentions |
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pubmed:dateCreated |
2008-3-28
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pubmed:abstractText |
Antigen-loaded dendritic cells (DCs) have been intensively investigated as potential cellular antitumor vaccines. Several recent reports have indicated that loading DCs with whole tumor derived mRNA or defined tumor-antigen-encoding mRNA represents an effective nonviral strategy to stimulate T cell responses both for in vitro and in vivo models. Here, we describe the electroporation method as a tool for introducing in vitro transcribed capped mRNA into human DCs for tumor vaccination. We use MART-1/Melan-A as a model tumor-associated antigen for the generation of a DC-based vaccine against melanoma cancer. In addition to efficient antigen loading, it is important to obtain a maximal number of potent antigen-presenting cells. Another prerequisite for the development of a DC-based cancer vaccine is to obtain mature DCs. In this chapter, we describe the basic techniques required for the successful genetic modification of DCs by using the mRNA electroporation method.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Neoplasm,
http://linkedlifedata.com/resource/pubmed/chemical/Cancer Vaccines,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/MART-1 Antigen,
http://linkedlifedata.com/resource/pubmed/chemical/MLANA protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Neoplasm Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/RNA Caps
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pubmed:status |
MEDLINE
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pubmed:issn |
1064-3745
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
423
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
155-63
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:18370196-Antigens, Neoplasm,
pubmed-meshheading:18370196-Base Sequence,
pubmed-meshheading:18370196-Cancer Vaccines,
pubmed-meshheading:18370196-Cell Separation,
pubmed-meshheading:18370196-DNA Primers,
pubmed-meshheading:18370196-Dendritic Cells,
pubmed-meshheading:18370196-Electrochemotherapy,
pubmed-meshheading:18370196-Electroporation,
pubmed-meshheading:18370196-Humans,
pubmed-meshheading:18370196-MART-1 Antigen,
pubmed-meshheading:18370196-Melanoma,
pubmed-meshheading:18370196-Mutagenesis, Site-Directed,
pubmed-meshheading:18370196-Neoplasm Proteins,
pubmed-meshheading:18370196-Plasmids,
pubmed-meshheading:18370196-RNA, Messenger,
pubmed-meshheading:18370196-RNA Caps,
pubmed-meshheading:18370196-T-Lymphocytes
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pubmed:year |
2008
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pubmed:articleTitle |
Delivery of tumor-antigen-encoding mRNA into dendritic cells for vaccination.
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pubmed:affiliation |
Department of Physiology and Immunology, Medical School of the Vrije Universiteit Brussel , Brussels, Belgium.
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pubmed:publicationType |
Journal Article
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