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CT043, a Protective Antigen That Induces a CD4+Th1 Response duringChlamydia trachomatisInfection in Mice and Humans

Authors :
Luisanna Zedda
Elisabetta Frigimelica
Nathalie Norais
Roberto Cevenini
Elisa Faenzi
Manuela Donati
Ilaria Ferlenghi
Mauro Agnusdei
Alessandra Bonci
Serena Giovinazzi
Francesca Buricchi
Guido Grandi
Giuliano Galli
Oretta Finco
Erika Bartolini
Roberto Petracca
Eva Meoni
Renata Grifantini
David A. G. Skibinski
Filomena Nardelli
Meoni E.
Faenzi E.
Frigimelica E.
Zedda L.
Skibinski D.
Giovinazzi S.
Bonci A.
Petracca R.
Bartolini E.
Galli G.
Agnusdei M.
Nardelli F.
Buricchi F.
Norais N.
Ferlenghi I.
Donati M.
Cevenini R.
Finco O.
Grandi G.
Grifantini R.
Source :
Infection and Immunity. 77:4168-4176
Publication Year :
2009
Publisher :
American Society for Microbiology, 2009.

Abstract

Despite several decades of intensive studies, no vaccines againstChlamydia 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 diagnosedC. trachomatisgenital 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 fromC. trachomatishuman 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 againstC. trachomatisinfection.

Details

ISSN :
10985522 and 00199567
Volume :
77
Database :
OpenAIRE
Journal :
Infection and Immunity
Accession number :
edsair.doi.dedup.....30dfecc2ef4f4279f5f85afcb7b7e5f1
Full Text :
https://doi.org/10.1128/iai.00344-09