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identifier: 1340957
description:
epitope description:DPNANPNVDPNANPNVNANPNANPNANP
host organism:Mus musculus C57BL/10
antibody name:Mouse sera
aggregation:
instance of dataset
availability:
available
primaryPublications: 9569470
authorizations:
registration not required
accessURL: http://www.iedb.org/reference/1002850
landingPage: http://www.iedb.org/assay/1340957
type:
Literature
publicationVenue:
Vaccine
dates:
1998
study type: b cell assays
subject species:
fullName:
E H Nardin
J M Calvo-Calle
G A Oliveira
P Clavijo
R Nussenzweig
R Simon
W Zeng
K Rose
method:
ELISA
name:
Plasmodium falciparum polyoximes: highly immunogenic synthetic vaccines constructed by chemoselective ligation of repeat B-cell epitopes and a universal T-cell epitope of CS protein.
description:
The CSP B repeat epitopes were combined in tetrabranched, di- and tri-epitope constructs with and without a T-helper epitope. The combined peptide sequence was derived from the CS protein of P. falciparum (NF54).
In high responder C57BL/10 (H-2b) mice, the T1B4 polypeptide, constructed by either chemoligation (polyoxime) or stepwise synthesis (MAP) were immunogenic with or without adjuvant (Alum). In the absence of adjuvant, peak titers were 6-fold higher for polyoxime the T1B4 immunized mice. Inclusion of the Pam3Cys adjuvant in the T1B4 polyoxime construct significantly enhanced its immunogenicity. A single injection elicited positive responses in all three mouse strains tested. Similarly, very high titers were measured for Pam3Cys-T1B4 polyoxime immunized C57BL/10 mice by immunofluorescence assay (IFA).

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