Skip navigation
Skip navigation

Development of a synthetic consensus sequence scrambled antigen HIV-1 vaccine designed for global use

Thomson, Scott; Jaramillo, Angel B; Shoobridge, Maryanne; Dunstan, Kerrie J; Everett, Beth; Kent, Stephen J; Gao, Ke; Medveczky, C; Ffrench, Rosemary A; Ramshaw, Ian; Ranasinghe, Charani

Description

Induction of high levels of broadly reactive cytotoxic T lymphocytes (CTL) remains a promising approach for an effective HIV-1 vaccine. We have developed a novel genetic-based vaccine strategy that encodes consensus overlapping peptide sets from all HIV-1 proteins scrambled together. This synthetic scrambled antigen vaccine (SAVINE) strategy has significant advantages, e.g. capacity to encode more antigens safely and is very flexible compared to traditional isolate-based strategies. The SAVINE...[Show more]

dc.contributor.authorThomson, Scott
dc.contributor.authorJaramillo, Angel B
dc.contributor.authorShoobridge, Maryanne
dc.contributor.authorDunstan, Kerrie J
dc.contributor.authorEverett, Beth
dc.contributor.authorKent, Stephen J
dc.contributor.authorGao, Ke
dc.contributor.authorMedveczky, C
dc.contributor.authorFfrench, Rosemary A
dc.contributor.authorRamshaw, Ian
dc.contributor.authorRanasinghe, Charani
dc.date.accessioned2015-12-13T23:00:13Z
dc.identifier.issn0264-410X
dc.identifier.urihttp://hdl.handle.net/1885/84024
dc.description.abstractInduction of high levels of broadly reactive cytotoxic T lymphocytes (CTL) remains a promising approach for an effective HIV-1 vaccine. We have developed a novel genetic-based vaccine strategy that encodes consensus overlapping peptide sets from all HIV-1 proteins scrambled together. This synthetic scrambled antigen vaccine (SAVINE) strategy has significant advantages, e.g. capacity to encode more antigens safely and is very flexible compared to traditional isolate-based strategies. The SAVINE vaccine strategy is clearly immunogenic, being able to restimulate a range of human HIV-1 specific responses in vitro and induce HIV-1 specific immunity in vivo in mice. Interestingly, different in vivo delivery strategies affected the resulting immunity and immunodominance pattern in mice. This platform strategy could be used for other infections and cancers where T cell responses are important for protection.
dc.publisherElsevier
dc.sourceVaccine
dc.subjectKeywords: Human immunodeficiency virus antigen; Human immunodeficiency virus vaccine; amino acid sequence; animal cell; animal experiment; article; cellular immunity; consensus sequence; controlled study; cytotoxic T lymphocyte; drug design; drug synthesis; female; Synthetic HIV vaccine
dc.titleDevelopment of a synthetic consensus sequence scrambled antigen HIV-1 vaccine designed for global use
dc.typeJournal article
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.citationvolume23
dc.date.issued2005
local.identifier.absfor110799 - Immunology not elsewhere classified
local.identifier.ariespublicationMigratedxPub12290
local.type.statusPublished Version
local.contributor.affiliationThomson, Scott, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationJaramillo, Angel B, University of New South Wales
local.contributor.affiliationShoobridge, Maryanne, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationDunstan, Kerrie J, University of New South Wales
local.contributor.affiliationEverett, Beth, University of New South Wales
local.contributor.affiliationRanasinghe, Charani, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationKent, Stephen J, University of Melbourne
local.contributor.affiliationGao, Ke, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationMedveczky, C, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationFfrench, Rosemary A, University of New South Wales
local.contributor.affiliationRamshaw, Ian, College of Medicine, Biology and Environment, ANU
local.description.embargo2037-12-31
local.bibliographicCitation.startpage4647
local.bibliographicCitation.lastpage4657
local.identifier.doi10.1016/j.vaccine.2005.04.045
dc.date.updated2015-12-12T07:32:41Z
local.identifier.scopusID2-s2.0-23644454804
CollectionsANU Research Publications

Download

File Description SizeFormat Image
01_Thomson_Development_of_a_synthetic_2005.pdf536.52 kBAdobe PDF    Request a copy


Items in Open Research are protected by copyright, with all rights reserved, unless otherwise indicated.

Updated:  17 November 2022/ Responsible Officer:  University Librarian/ Page Contact:  Library Systems & Web Coordinator