| Literature DB >> 24968155 |
Pavla Simerska1, Tittaya Suksamran2, Zyta Maria Ziora2, Fabian de Labastida Rivera3, Christian Engwerda3, Istvan Toth4.
Abstract
The lipid core peptide (LCP) system has successfully been used in development of peptide-based vaccines against cancer and infectious diseases (such as group A streptococcal infection). CD8(+) T cells are important targets for vaccines, however developing a vaccine that activates long-lasting immunity has proven challenging. The ability of LCP vaccines to activate antigen-specific CD8(+) and/or CD4(+) T cell responses was tested using compounds that contained two or four copies of OVA257-264 and/or OVA323-339 peptides conjugated to LCP, which are recognised by OTI (CD8(+) specific) and OTII (CD4(+) specific) T cells, respectively. The LCP-ovalbumin vaccines developed in this study were synthesised in 30% yields and showed no significant haemolytic effect on red blood cells (below 4% haemolysis when tested with compounds at up to 100μM concentrations). Promising in vivo data in mice suggested that this LCP-ovalbumin vaccine system could act as a novel and potent vehicle for the stimulation of robust antigen-specific CD8(+) T cell responses.Entities:
Keywords: CD4(+); CD8(+); Ovalbumin; Peptide synthesis; T cell; Vaccine development
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Year: 2014 PMID: 24968155 DOI: 10.1016/j.vaccine.2014.06.049
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641