Source:http://linkedlifedata.com/resource/pubmed/id/20060510
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2010-3-1
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pubmed:abstractText |
Here we demonstrated that bis-(3',5')-cyclic dimeric inosine monophosphate (c-di-IMP) exhibits potent adjuvant properties. BALB/c or C57BL/6 mice were immunized with the model antigens beta-galactosidase (beta-Gal) or Ovalbumin (OVA) alone or co-administered with c-di-IMP by the intranasal route. Animals receiving c-di-IMP showed significantly higher anti-beta-Gal or OVA immunoglobulin G titres (IgG) in sera than those vaccinated with beta-Gal or OVA alone. Furthermore, strong local immune responses were also detectable in different mucosal territories, as shown by the high levels of beta-Gal-specific secretory IgA (sIgA). The analysis of the antigen-specific IgG isotypes in sera, together with the profiles of the cytokines and chemokines secreted by lymphocytes from vaccinated animals showed that the use of c-di-IMP resulted in stimulation of a mixed T(H)1/T(H)2/T(H)17 response. Mucosal immunization of C57BL/6 mice with OVA using c-di-IMP as adjuvant also led to the stimulation of strong in vivo CTL responses (i.e., 60% of antigen-specific lysis) [corrected].Our results demonstrated that the novel compound c-di-IMP exhibits strong adjuvant properties when co-administered with an antigen by the mucosal route, thereby representing a promising candidate adjuvant for the development of mucosal vaccination strategies.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adjuvants, Immunologic,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclic IMP,
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin A, Secretory,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Ovalbumin,
http://linkedlifedata.com/resource/pubmed/chemical/beta-Galactosidase
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1873-2518
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2009 Elsevier Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
2
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pubmed:volume |
28
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2249-58
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pubmed:meshHeading |
pubmed-meshheading:20060510-Adjuvants, Immunologic,
pubmed-meshheading:20060510-Administration, Intranasal,
pubmed-meshheading:20060510-Animals,
pubmed-meshheading:20060510-Cyclic IMP,
pubmed-meshheading:20060510-Cytokines,
pubmed-meshheading:20060510-Cytotoxicity, Immunologic,
pubmed-meshheading:20060510-Female,
pubmed-meshheading:20060510-Humans,
pubmed-meshheading:20060510-Immunity, Mucosal,
pubmed-meshheading:20060510-Immunoglobulin A, Secretory,
pubmed-meshheading:20060510-Immunoglobulin G,
pubmed-meshheading:20060510-Lymphocytes,
pubmed-meshheading:20060510-Mice,
pubmed-meshheading:20060510-Mice, Inbred BALB C,
pubmed-meshheading:20060510-Mice, Inbred C57BL,
pubmed-meshheading:20060510-Ovalbumin,
pubmed-meshheading:20060510-beta-Galactosidase
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pubmed:year |
2010
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pubmed:articleTitle |
The member of the cyclic di-nucleotide family bis-(3', 5')-cyclic dimeric inosine monophosphate exerts potent activity as mucosal adjuvant.
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pubmed:affiliation |
Department of Vaccinology and Applied Microbiology, Helmholtz Centre of Infection Research, Inhoffenstrasse 7, D-38124 Braunschweig, Germany.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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