| Literature DB >> 20870056 |
Anna Kabanova1, Immaculada Margarit, Francesco Berti, Maria R Romano, Guido Grandi, Giuliano Bensi, Emiliano Chiarot, Daniela Proietti, Erwin Swennen, Emilia Cappelletti, Paola Fontani, Daniele Casini, Roberto Adamo, Vittoria Pinto, David Skibinski, Sabrina Capo, Giada Buffi, Marilena Gallotta, William J Christ, A Stewart Campbell, John Pena, Peter H Seeberger, Rino Rappuoli, Paolo Costantino.
Abstract
Bacterial infections caused by Group A Streptococcus (GAS) are a serious health care concern that currently cannot be prevented by vaccination. The GAS cell-wall polysaccharide (GAS-PS) is an attractive vaccine candidate due to its constant expression pattern on different bacterial strains and protective properties of anti-GAS-PS antibodies. Here we report for the first time the immunoprotective efficacy of glycoconjugates with synthetic GAS oligosaccharides as compared to those containing the native GAS-PS. A series of hexa- and dodecasaccharides based on the GAS-PS structure were prepared by chemical synthesis and conjugated to CRM(197). When tested in mice, the conjugates containing the synthetic oligosaccharides conferred levels of immunoprotection comparable to those elicited by the native conjugate. Antisera from immunized rabbits promoted phagocytosis of encapsulated GAS strains. Furthermore we discuss variables that might correlate with glycoconjugate immunogenicity and demonstrate the potential of the synthetic approach that benefits from increased antigen purity and facilitated manufacturing.Entities:
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Year: 2010 PMID: 20870056 DOI: 10.1016/j.vaccine.2010.09.018
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641