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Lipid core peptides provide novel self-adjuvanting vaccine delivery system.

Vaccine Weekly

| July 02, 2003 | COPYRIGHT 2003 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2003 JUL 2 - (NewsRx.com & NewsRx.net) -- Lipid core peptide technology shows promise as a novel self-adjuvanting vaccine delivery system for multiple different synthetic peptide immunogens.

"This study demonstrates the effectiveness of a novel self-adjuvanting vaccine delivery system for multiple different synthetic peptide immunogens by use of lipid core peptide (LCP) technology. An LCP formulation incorporating two different protective epitopes of the surface antiphagocytic M protein of group A streptococci (GAS)-the causative agents of rheumatic fever and subsequent rheumatic heart disease-was tested in a murine parenteral immunization and GAS challenge model," researchers in Australia report.

"Mice were immunized with the LCP-GAS formulation, which contains an M protein amino-terminal type-specific peptide sequence (8830) in combination with a conserved non-host-cross-reactive carboxy-terminal C-region peptide sequence (J8) of the M protein," stated Colleen Olive and collaborators at the Queensland Institute of Medical Research and the University of Queensland. "Our data demonstrated immunogenicity of the LCP-8830-J8 formulation in B10.BR mice when co-administered in complete Freund's adjuvant and in the absence of a conventional adjuvant. In both cases, immunization led to induction of high-titer GAS peptide-specific serum immunoglobulin G antibody responses and induction of highly opsonic antibodies that did not cross-react with human heart tissue proteins.

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