rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
8
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pubmed:dateCreated |
1997-10-23
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pubmed:abstractText |
Past attempts to use fractions of mycobacteria as an alternative to BCG have given disappointing results. The availability of cloned genes and suitable vectors has now opened a new avenue in which individual mycobacterial protein antigens are synthesised within transfected mammalian cells. In an ex vivo transfection approach with a retroviral vector we found that even a single antigen (hsp65) could evoke strong protection when expressed as a transgene and that expression of protection was largely a function of antigen specific cytotoxic T cells. We now find that intramuscular injection of plasmid DNA expressing the antigen from either a viral or a murine promoter can also give protection equivalent to Bacillus Calmette-Guérin (BCG). Plasmids expressing some other mycobacterial antigens, hsp70, 36 kDa and 6 kDa, are also effective, suggesting that this approach may lead to a new vaccine.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Bacterial,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Bacterial,
http://linkedlifedata.com/resource/pubmed/chemical/BCG Vaccine,
http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Chaperonin 60,
http://linkedlifedata.com/resource/pubmed/chemical/Chaperonins,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Vaccines, DNA,
http://linkedlifedata.com/resource/pubmed/chemical/heat-shock protein 65, Mycobacterium
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0264-410X
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
834-8
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:9234527-Animals,
pubmed-meshheading:9234527-Antibodies, Bacterial,
pubmed-meshheading:9234527-Antigens, Bacterial,
pubmed-meshheading:9234527-BCG Vaccine,
pubmed-meshheading:9234527-Bacterial Proteins,
pubmed-meshheading:9234527-Chaperonin 60,
pubmed-meshheading:9234527-Chaperonins,
pubmed-meshheading:9234527-Clone Cells,
pubmed-meshheading:9234527-Injections, Intramuscular,
pubmed-meshheading:9234527-Interferon-gamma,
pubmed-meshheading:9234527-Mice,
pubmed-meshheading:9234527-Mice, Inbred BALB C,
pubmed-meshheading:9234527-Mice, Inbred CBA,
pubmed-meshheading:9234527-Mycobacterium leprae,
pubmed-meshheading:9234527-Plasmids,
pubmed-meshheading:9234527-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:9234527-Tuberculosis,
pubmed-meshheading:9234527-Vaccines, DNA
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pubmed:year |
1997
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pubmed:articleTitle |
Protection against tuberculosis by a plasmid DNA vaccine.
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pubmed:affiliation |
NIMR, London, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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