Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2010-11-25
pubmed:abstractText
The C-terminal fragment of Clostridium perfringens enterotoxin (C-CPE) is a claudin-4 binder. Very recently, we found that nasal immunization of mice with C-CPE-fused antigen activated antigen-specific humoral and mucosal immune responses and that the deletion of the claudin-4-binding domain attenuated the immune responses. C-CPE-fusion strategy may be useful for mucosal vaccination. C-CPE is a fragment of enterotoxin, and the safety of C-CPE-fused protein is very important for its future application. In the present study, we investigated whether C-CPE-fused antigen induces immune responses without mucosal injury by using ovalbumin (OVA) as a model antigen. Immunohistochemical analysis showed that claudin-4 was expressed in epithelial cell sheets bordering the nasal cavity. Nasal immunization with C-CPE-fused OVA dose-dependently elevated the OVA-specific serum IgG titer, which was 1000-fold greater than the titer achieved by immunization with OVA or a mixture of OVA and C-CPE at 5 microg of OVA. Nasal immunization with C-CPE-fused OVA (5 microg of OVA) activated Th1 and Th2 responses. Histological analysis showed no mucosal injury in the nasal cavity or nasal passage. C-CPE-fused OVA exhibited mucosal vaccination without mucosal injury. These findings indicate thatclaudin-4-targeting using C-CPE can be a potent strategy for mucosal vaccination.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0031-7144
pubmed:author
pubmed:issnType
Print
pubmed:volume
65
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
766-9
pubmed:meshHeading
pubmed-meshheading:21105580-Administration, Intranasal, pubmed-meshheading:21105580-Animals, pubmed-meshheading:21105580-Clostridium Infections, pubmed-meshheading:21105580-Clostridium perfringens, pubmed-meshheading:21105580-Dose-Response Relationship, Immunologic, pubmed-meshheading:21105580-Enterotoxins, pubmed-meshheading:21105580-Female, pubmed-meshheading:21105580-Immunity, Mucosal, pubmed-meshheading:21105580-Immunoglobulin G, pubmed-meshheading:21105580-Immunohistochemistry, pubmed-meshheading:21105580-Membrane Proteins, pubmed-meshheading:21105580-Mice, pubmed-meshheading:21105580-Mice, Inbred BALB C, pubmed-meshheading:21105580-Ovalbumin, pubmed-meshheading:21105580-Peptide Fragments, pubmed-meshheading:21105580-Th1 Cells, pubmed-meshheading:21105580-Th2 Cells, pubmed-meshheading:21105580-Vaccines, Subunit
pubmed:year
2010
pubmed:articleTitle
The safety of a mucosal vaccine using the C-terminal fragment of Clostridium perfringens enterotoxin.
pubmed:affiliation
Laboratory of Bio-Functional Molecular Chemistry, Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't