| Literature DB >> 19596772 |
Eva Meoni1, Elisa Faenzi, Elisabetta Frigimelica, Luisanna Zedda, David Skibinski, Serena Giovinazzi, Alessandra Bonci, Roberto Petracca, Erika Bartolini, Giuliano Galli, Mauro Agnusdei, Filomena Nardelli, Francesca Buricchi, Nathalie Norais, Ilaria Ferlenghi, Manuela Donati, Roberto Cevenini, Oretta Finco, Guido Grandi, Renata Grifantini.
Abstract
Despite several decades of intensive studies, no vaccines against Chlamydia trachomatis, an intracellular pathogen causing serious ocular and urogenital diseases, are available yet. Infection-induced immunity in both animal models and humans strongly supports the notion that for a vaccine to be effective a strong CD4(+) Th1 immune response should be induced. In the course of our vaccine screening program based on the selection of chlamydial proteins eliciting cell-mediated immunity, we have found that CT043, a protein annotated as hypothetical, induces CD4(+) Th1 cells both in chlamydia-infected mice and in human patients with diagnosed C. trachomatis genital infection. DNA priming/protein boost immunization with CT043 results in a 2.6-log inclusion-forming unit reduction in the murine lung infection model. Sequence analysis of CT043 from C. trachomatis human isolates belonging to the most representative genital serovars revealed a high degree of conservation, suggesting that this antigen could provide cross-serotype protection. Therefore, CT043 is a promising vaccine candidate against C. trachomatis infection.Entities:
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Year: 2009 PMID: 19596772 PMCID: PMC2738022 DOI: 10.1128/IAI.00344-09
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441