Abstract |
Despite the strong immune responses elicited after natural infection with Trypanosoma cruzi or vaccination against it, parasite survival suggests that these responses are insufficient or inherently inadequate. T. cruzi contains a major cystein proteinase, cruzipain, which has a catalytic N-terminal domain and a C-terminal extension. Immunizations that employed recombinant cruzipain or its N- and C-terminal domains allowed evaluation of the ability of cruzipain to circumvent responses against the catalytic domain. This phenomenon is not a property of the parasite but of cruzipain itself, because recombinant cruzipain triggers a response similar to that of cruzipain during natural or experimental infection. Cruzipain is not the only antigen with a highly immunogenic region of unknown function that somehow protects an essential domain for parasite survival. However, our studies show that this can be reverted by using the N-terminal domain as a tailored immunogen able to redirect host responses to provide enhanced protection.
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Authors | Silvia I Cazorla, Fernanda M Frank, Pablo D Becker, María Arnaiz, Gerardo A Mirkin, Ricardo S Corral, Carlos A Guzmán, Emilio L Malchiodi |
Journal | The Journal of infectious diseases
(J Infect Dis)
Vol. 202
Issue 1
Pg. 136-44
(Jul 01 2010)
ISSN: 1537-6613 [Electronic] United States |
PMID | 20497050
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies, Protozoan
- Protozoan Proteins
- Protozoan Vaccines
- Recombinant Proteins
- Cysteine Endopeptidases
- cruzipain
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Topics |
- Animals
- Antibodies, Protozoan
(blood)
- Chagas Disease
(prevention & control)
- Cysteine Endopeptidases
(immunology)
- Female
- Mice
- Mice, Inbred C3H
- Muscle, Skeletal
(pathology)
- Myocardium
(pathology)
- Protozoan Proteins
(immunology)
- Protozoan Vaccines
(immunology)
- Recombinant Proteins
(immunology)
- Trypanosoma cruzi
(enzymology, genetics, immunology)
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