| Literature DB >> 12559784 |
Manuela Donati1, Vittorio Sambri, Maurizio Comanducci, Korinne Di Leo, Elisa Storni, Lorenzo Giacani, Giulio Ratti, Roberto Cevenini.
Abstract
Chlamydia trachomatis pgp3 DNA immunized (no. 300) and non-immunized (no. 300) C3H/HeN mice were infected by vaginal inoculation with infectious C. trachomatis serotype D elementary bodies (EBs) and the spread of infection to the salpinges was assessed by cell culture isolation from tissue homogenates 7, 14, 21, 28, 35 and 42 days post-infection (p.i.). Overall, the pgp3-DNA immunization prevented salpinx infection in 94 (56%) mice, if compared with the 168 positive animals found among the non-immunized animals (P < 0.001). A group of negative control animals (i.e. mice immunized with plasmid DNA containing an irrelevant insert) was not protected, whereas all the mice of a positive immune control group (mice that had resolved a primary genital C. trachomatis infection) were resistant to re-infection. Pgp3 DNA immunization induced both humoral and mucosal anti-pgp3 antibodies. Copyright 2002 Elsevier Science Ltd.Entities:
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Year: 2003 PMID: 12559784 DOI: 10.1016/s0264-410x(02)00631-x
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641