Source:http://linkedlifedata.com/resource/pubmed/id/10194445
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
1999-5-3
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pubmed:abstractText |
Granulocyte-macrophage colony-stimulating factor (GM-CSF) is an important cytokine for the generation and propagation of antigen-presenting cells and for priming a cellular immune response. We report here that use of recombinant human GM-CSF (rhGM-CSF), administered as an adjuvant in a peptide-based vaccine trial given monthly by intradermal injection, led to the development of a T-cell and antibody response to rhGM-CSF. An antibody response occurred in the majority of patients (72%). This antibody response was not found to be neutralizing. In addition, by 48-hour delayed type hypersensitivity (DTH) skin testing, 17% of patients were shown to have a cellular immune response to the adjuvant rhGM-CSF alone. Thymidine incorporation assays also showed a peripheral blood T-cell response to rhGM-CSF in at least 17% of the patients. The generation of rhGM-CSF-specific T-cell immune responses, elicited in this fashion, is an important observation because rhGM-CSF is being used as a vaccine adjuvant in various vaccine strategies. rhGM-CSF-specific immune responses may be incorrectly interpreted as antigen-specific immunity, particularly when local DTH responses to vaccination are the primary means of immunologic evaluation. We found no evidence of hematologic or infectious complications as a result of the development of rhGM-CSF-specific immune responses.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adjuvants, Immunologic,
http://linkedlifedata.com/resource/pubmed/chemical/Granulocyte-Macrophage...,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Vaccines, Synthetic
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0006-4971
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
93
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
2653-9
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:10194445-Adjuvants, Immunologic,
pubmed-meshheading:10194445-Antibody Formation,
pubmed-meshheading:10194445-CD4-Positive T-Lymphocytes,
pubmed-meshheading:10194445-CD8-Positive T-Lymphocytes,
pubmed-meshheading:10194445-Cell Line,
pubmed-meshheading:10194445-Granulocyte-Macrophage Colony-Stimulating Factor,
pubmed-meshheading:10194445-Humans,
pubmed-meshheading:10194445-Hypersensitivity, Delayed,
pubmed-meshheading:10194445-Immunity, Cellular,
pubmed-meshheading:10194445-Immunoglobulin G,
pubmed-meshheading:10194445-Injections, Intradermal,
pubmed-meshheading:10194445-Recombinant Proteins,
pubmed-meshheading:10194445-Skin Tests,
pubmed-meshheading:10194445-T-Lymphocytes,
pubmed-meshheading:10194445-Time Factors,
pubmed-meshheading:10194445-Vaccines, Synthetic
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pubmed:year |
1999
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pubmed:articleTitle |
Immunization with recombinant human granulocyte-macrophage colony-stimulating factor as a vaccine adjuvant elicits both a cellular and humoral response to recombinant human granulocyte-macrophage colony-stimulating factor.
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pubmed:affiliation |
Division of Oncology, University of Washington, Seattle, WA, USA.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, U.S. Gov't, P.H.S.,
Clinical Trial, Phase I
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