Source:http://linkedlifedata.com/resource/pubmed/id/15161067
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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0003241,
umls-concept:C0012550,
umls-concept:C0020971,
umls-concept:C0039194,
umls-concept:C0086418,
umls-concept:C0162969,
umls-concept:C0205263,
umls-concept:C0442118,
umls-concept:C0524527,
umls-concept:C0871261,
umls-concept:C1627358,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C2349975,
umls-concept:C2911692
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pubmed:issue |
8
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pubmed:dateCreated |
2004-5-26
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pubmed:abstractText |
We previously reported that intranasal immunization with a non-toxic mutant cross-reacting material (CRM)197 of diphtheria toxin, formulated with chitosan, generated protective neutralizing antibodies in mice and guinea pigs. Furthermore, we demonstrated that intranasal delivery of a powder formulation of the CRM197-based vaccine was well tolerated and significantly boosted antibody responses in adult volunteers. Here we report that intranasal booster immunization with CRM197 alone or with chitosan induced systemic T cell responses. We addressed for the first time the induction of T cell subtypes following intranasal vaccination in humans. Intranasal vaccination with CRM197, like parenteral immunization with a conventional diphtheria toxoid vaccine, enhanced antigen-specific IFN-gamma production. However, formulation of the nasal diphtheria vaccine with chitosan significantly augmented Th2-type responses, which correlated with protective levels of toxin-neutralizing antibodies in intranasally boosted individuals. The results suggest that vaccines capable of inducing strong Th2-type responses, such as CRM197 formulated with chitosan, have potential for the development of a protective mucosal vaccine against diphtheria in humans. Furthermore, our findings demonstrate that mucosal subunit vaccines with appropriate delivery systems have considerable potential for booster immunization of adults.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0264-410X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
25
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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 |
909-14
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15161067-Administration, Intranasal,
pubmed-meshheading:15161067-Adolescent,
pubmed-meshheading:15161067-Adult,
pubmed-meshheading:15161067-Antibodies, Bacterial,
pubmed-meshheading:15161067-Chemistry, Pharmaceutical,
pubmed-meshheading:15161067-Chitin,
pubmed-meshheading:15161067-Chitosan,
pubmed-meshheading:15161067-Diphtheria Toxin,
pubmed-meshheading:15161067-Female,
pubmed-meshheading:15161067-Humans,
pubmed-meshheading:15161067-Male,
pubmed-meshheading:15161067-Nasal Mucosa,
pubmed-meshheading:15161067-Th2 Cells
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pubmed:year |
2004
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pubmed:articleTitle |
Intranasal immunization with genetically detoxified diphtheria toxin induces T cell responses in humans: enhancement of Th2 responses and toxin-neutralizing antibodies by formulation with chitosan.
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pubmed:affiliation |
Immune Regulation Research Group, Department of Biochemistry, Trinity College, Dublin 2, Ireland.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Controlled Clinical Trial,
Research Support, Non-U.S. Gov't
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