Affiliation:
1. Department of Cellular Biology and Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, Georgia 30502
Abstract
ABSTRACT
Trypanosoma cruzi
infects millions of people in Latin America and often leads to the development of Chagas disease.
T. cruzi
infection can be acquired at or near the bite site of the triatomine vector, but
per os
infection is also a well-documented mode of transmission, as evidenced by recent microepidemics of acute Chagas disease attributed to the consumption of parasite-contaminated foods and liquids. It would also be convenient to deliver vaccines for
T. cruzi
by the oral route, particularly live parasite vaccines intended for the immunization of reservoir hosts. For these reasons, we were interested in better understanding immunity to
T. cruzi
following oral infection or oral vaccination, knowing that the route of infection and site of antigen encounter can have substantial effects on the ensuing immune response. Here, we show that the route of infection does not alter the ability of
T. cruzi
to establish infection in muscle tissue nor does it impair the generation of a robust CD8
+
T cell response. Importantly, oral vaccination with attenuated parasites provides protection against wild-type (WT)
T. cruzi
challenge. These results strongly support the development of whole-organism-based vaccines targeting reservoir species as a means to alleviate the burden of Chagas disease in affected regions.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
33 articles.
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