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Infection and Immunity, September 2000, p. 4948-4953, Vol. 68, No. 9
Department of Applied Genetics, Institut de
Biologie et de Médecine Moléculaires, Université
Libre de Bruxelles, B-6041 Gosselies,1 and
SmithKline Beecham Biologicals, B-1330
Rixensart,2 Belgium
Received 13 April 2000/Returned for modification 30 May
2000/Accepted 7 June 2000
Primary infection with Toxoplasma gondii during
pregnancy can induce fetal pathology and abortion in both humans and
animals. The present study describes the development of an experimental model of congenital toxoplasmosis in the guinea pig. In this animal model, we evaluated the protective effect of vaccination with a
recombinant form of SAG1 against maternofetal transmission of tachyzoites. The presence of parasites in fetuses was determined by
nested PCRs and by an in vivo readout after fetal brain homogenate injections in mice. The absence of parasites was demonstrated in 66 to
86% of fetuses derived from adult guinea pigs immunized with SAG1 and
challenged with the mildly virulent T. gondii strain C56.
In contrast, more than 80% of fetuses from mock-immunized guinea pigs
were infected. The protection was not correlated with titers of
antibody to SAG1. Our results indicated that this experimental model
constitutes a relevant model for evaluation of vaccine candidates against congenital toxoplasmosis and that SAG1 elicits significant protection against maternofetal transmission.
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Protective Immunity against Congenital
Toxoplasmosis with Recombinant SAG1 Protein in a Guinea Pig
Model
*
Corresponding author. Mailing address: Rue des
Professeurs Jeener et Brachet, 12, B-6041 Gosselies, Belgium. Phone: 32 2 650 99 09. Fax: 32 2 650 99 00. E-mail:
ajacquet{at}sga.ulb.ac.be.
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