A peptide carrier with a built-in vaccine adjuvant: Construction of immunogenic conjugates

dc.contributor.authorKrikorian, D.en
dc.contributor.authorPanou-Pomonis, E.en
dc.contributor.authorVoitharou, C.en
dc.contributor.authorSakarellos, C.en
dc.contributor.authorSakarellos-Daitsiotis, M.en
dc.date.accessioned2015-11-24T16:58:06Z
dc.date.available2015-11-24T16:58:06Z
dc.identifier.issn1043-1802-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10656
dc.rightsDefault Licence-
dc.subjectsequential oligopeptide carriersen
dc.subjectt-cell epitopesen
dc.subjectcircular-dichroismen
dc.subjectantigenic peptidesen
dc.subjectimmune-responsesen
dc.subjectb-cellen
dc.subjectautoantibodiesen
dc.subjectdeterminantsen
dc.subjectproteinsen
dc.subjectdiversificationen
dc.titleA peptide carrier with a built-in vaccine adjuvant: Construction of immunogenic conjugatesen
heal.abstractA multifunctional carrier combining B/T cell epitopes (i), a built-in vaccine adjuvant (ii), and a universal T cell epitope (iii) for the construction of potent and specific immunogenic conjugates is presented. The IL-1 beta(163-171) fragment known to reproduce the immunostimulatory and adjuvant effects of the whole IL-1 beta without possessing any of the pro-inflammatory properties of IL-1 beta was covalently anchored to the N-terminus of the Sequential Oligopeptide Carrier, SOCn, formed by the repeating tripeptide unit Lys-Aib-Gly. A promiscuous T cell epitope derived from the tetanus toxin, TT(593599), was also positioned in the carboxy terminus of SOCn, as a universal immunogen to provide broad immunogenicity. Selected B/T cell epitopes from the Sm and La/SSB autoantigens, against which is directed the humoral autoimmunity in patients with systemic lupus erythematosus and Sjogren's Syndrome, respectively, were coupled to the Lys-(NH2)-H-epsilon groups of the carrier, and the formulated constructs were administered in animals following the conventional immunization protocol of complete/incomplete Freund's adjuvant. The induced immune responses were compared with that produced when the Sm- and La/SSB-reconstituted immunogenic conjugates were injected alone. High titers of specific antibodies recognizing the priming construct, as well as the cognate autoantigen, were obtained when administered alone without the assistance of Freund's adjuvant. It is concluded that our approach provides the conceptual and experimental framework for the development of multifunctional immunogenic conjugates eliciting enhanced, specific, and prolonged humoral response for usage as human vaccine candidates.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDoi 10.1021/Bc049703m-
heal.identifier.secondary<Go to ISI>://000230712900009-
heal.identifier.secondaryhttp://pubs.acs.org/doi/abs/10.1021/bc049703m-
heal.journalNameBioconjugate Chemistryen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2005-
heal.publisherAmerican Chemical Societyen
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

Αρχεία

Φάκελος/Πακέτο αδειών

Προβολή: 1 - 1 of 1
Φόρτωση...
Μικρογραφία εικόνας
Ονομα:
license.txt
Μέγεθος:
1.74 KB
Μορφότυπο:
Item-specific license agreed upon to submission
Περιγραφή: