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Vaccine ; 38(48): 7645-7653, 2020 11 10.
Artículo en Inglés | MEDLINE | ID: mdl-33071003

RESUMEN

The development of a Chagas disease vaccine has yet the need for the identification of novel combinations of antigens and adjuvants. Here, the performance of TcTASV-C proteins that are virulence factors of trypomastigotes and belong to a novel surface protein family specific for T. cruzi, have been evaluated as antigens for a prophylactic vaccine. Several immunization schemes in which TcTASV-C was combined with aluminum hydroxide, saponin and/or U-Omp19 were assayed. Aluminum hydroxide and saponin were assayed together to trigger different pathways of the immune response simultaneously. U-Omp19 is a promising novel adjuvant able to promote a Th1 immune response with IFNg production, thus an interesting molecule to be tested as adjuvant for the control of T. cruzi infection. Therefore, U-Omp19 was added to the aluminum hydroxide-saponin formulation as well as assayed individually with TcTASV-C. The immunization with TcTASV-C and U-Omp19 had the best performance as a prophylactic vaccine. Mice presented the lowest parasitemias and improved survival by 40% after being challenged with a highly virulent T. cruzi strain, which promoted 100% mortality in all other immunized groups. Immunization with TcTASV-C and U-Omp19 triggered cellular responses with IFN-γ and IL-17 production and with lytic antibodies that could explain the protection achieved by this vaccination scheme. To our knowledge, this is the first time that U-Omp19 is tested with a defined T. cruzi antigen in a vaccine formulation.


Asunto(s)
Enfermedad de Chagas , Trypanosoma cruzi , Factores de Virulencia , Inmunidad Adaptativa , Adyuvantes Inmunológicos , Hidróxido de Aluminio , Animales , Anticuerpos Antiprotozoarios , Antígenos de Protozoos , Enfermedad de Chagas/inmunología , Enfermedad de Chagas/prevención & control , Ratones , Ratones Endogámicos BALB C , Trypanosoma cruzi/inmunología , Trypanosoma cruzi/patogenicidad
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