Source:http://linkedlifedata.com/resource/pubmed/id/15474704
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
31-32
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pubmed:dateCreated |
2004-10-11
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pubmed:abstractText |
Recombinant Bacillus subtilis spores were employed as a vaccine delivery system in a heterologous mucosal priming-parenteral boosting vaccination strategy in the mouse model. BALB/c and C57BL/6 mice were orally immunised with recombinant spores expressing tetanus toxin fragment C (TTFC) fused to the spore outer coat protein CotB, and then subcutaneously boosted with soluble TTFC (without adjuvant). Two weeks after boosting, a significantly higher serum TTFC-specific IgG response was stimulated in mice primed with recombinant spores (antibody concentration of 2600 +/- 915 in C57BL/6 and 1200 +/- 370 ng/ml in BALB/c) compared to mice inoculated with wild type spores (650 +/- 250 and 250 +/- 130 ng/ml, respectively). IgG subclass analysis showed a prevalence of IgG1 and IgG2b, indicative of a Th2 type of immune response. Oral administration of recombinant spores stimulated also a significant local TTFC-specific IgA response. These data show that recombinant spores of B. subtilis are able to prime the immune system by the oral route, and that a combined mucosal/parenteral strategy can stimulate both local and systemic antigen-specific immune responses.
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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/Bacterial Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/CotB protein, Bacillus subtilis,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin A,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Tetanus Toxin
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0264-410X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
22
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4139-43
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15474704-Animals,
pubmed-meshheading:15474704-Antibodies, Bacterial,
pubmed-meshheading:15474704-Bacillus subtilis,
pubmed-meshheading:15474704-Bacterial Proteins,
pubmed-meshheading:15474704-Female,
pubmed-meshheading:15474704-Immunoglobulin A,
pubmed-meshheading:15474704-Immunoglobulin G,
pubmed-meshheading:15474704-Mice,
pubmed-meshheading:15474704-Mice, Inbred BALB C,
pubmed-meshheading:15474704-Mice, Inbred C57BL,
pubmed-meshheading:15474704-Recombinant Proteins,
pubmed-meshheading:15474704-Spores, Bacterial,
pubmed-meshheading:15474704-Tetanus Toxin
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pubmed:year |
2004
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pubmed:articleTitle |
Oral priming of mice by recombinant spores of Bacillus subtilis.
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pubmed:affiliation |
Laboratorio di Microbiologia Molecolare e Biotecnologia (LAMMB), Dipartimento di Biologia Molecolare, Università di Siena, Policlinico Le Scotte V lotto, piano 1, 53100 Siena, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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