HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Redirection of the immune response to the functional catalytic domain of the cystein proteinase cruzipain improves protective immunity against Trypanosoma cruzi infection.

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.
AuthorsSilvia I Cazorla, Fernanda M Frank, Pablo D Becker, María Arnaiz, Gerardo A Mirkin, Ricardo S Corral, Carlos A Guzmán, Emilio L Malchiodi
JournalThe Journal of infectious diseases (J Infect Dis) Vol. 202 Issue 1 Pg. 136-44 (Jul 01 2010) ISSN: 1537-6613 [Electronic] United States
PMID20497050 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Antibodies, Protozoan
  • Protozoan Proteins
  • Protozoan Vaccines
  • Recombinant Proteins
  • Cysteine Endopeptidases
  • cruzipain
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)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: