Development of a Liposaccharide-Based Delivery System and Its Application to the Design of Group A Streptococcal Vaccines
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Abdel-Aal, Abu-Baker M.
Fujita, Yoshio
Moyle, Peter M.
McGeary, Ross P.
Batzloff, Michael R.
Olive, Colleen
Good, Michael F.
Toth, Istvan
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Abstract
Group A streptococcus (GAS) is associated with many human diseases, ranging in severity from benign to life-threatening. A promising strategy for developing vaccines against GAS involves the use of carbohydrates as carriers for peptide antigens. This study describes the optimized synthesis of d-glucose and d-galactose derived carriers, bearing an adipate linker and four tert-butoxycarbonyl protected aminopropyl groups. Prophylactic GAS vaccine candidates were synthesized by conjugating multiple copies of a single GAS M protein derived peptide antigen (either J8 or J14) onto the carbohydrate carriers. These antigens contain peptide sequences, which are highly conserved and offer the potential to prevent infections caused by up to 70% of GAS strains. Lipophilic amino acids were also conjugated to the d-glucose anomeric carbon to produce a self-adjuvanting liposaccharide vaccine. High serum IgG antibody titers against each of the incorporated peptide epitopes were detected following subcutaneous immunization of B10.BR (H-2k) mice with the liposaccharide vaccine candidates.
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Journal of Medicinal Chemistry
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51
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5
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Infectious Agents