Resiniferatoxin modulates the Th1 immune response and protects the host during intestinal nematode infection

In the early stage of the intestinal phase of Trichinella spiralis infection, the host triggers a Th1-type immune response with the aim of eliminating the parasite. However, this response damages the host which favours the survival of the parasite. In the search for novel pharmacological strategies...

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Detalles Bibliográficos
Autores: Muñoz Carrillo, José Luís, Contreras Cordero, Juan Francisco, Muñoz López, José Luis, Maldonado Tapia, Claudia, Muñoz Escobedo, José Jesús, Moreno García, María Alejandra
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2017
País:México
Institución:Universidad Autónoma de Zacatecas
Repositorio:Repositorio Institucional Caxcán
Idioma:inglés
OAI Identifier:oai:http://ricaxcan.uaz.edu.mx:20.500.11845/708
Acceso en línea:http://localhost/xmlui/handle/20.500.11845/708
https://doi.org/10.48779/tn6m-my91
Access Level:acceso abierto
Palabra clave:BIOLOGIA Y QUIMICA [2]
immune response
resiniferatoxin
Th1 cytokines
Trichinella spiralis
Descripción
Sumario:In the early stage of the intestinal phase of Trichinella spiralis infection, the host triggers a Th1-type immune response with the aim of eliminating the parasite. However, this response damages the host which favours the survival of the parasite. In the search for novel pharmacological strategies that inhibit the Th1 immune response and assist the host against T. spiralis infection, a recent study showed that resiniferatoxin had anti-inflammatory activity contributed to the host in T. spiralis infection. In this study, we evaluated whether RTX modulates the host immune response through the inhibition of Th1 cytokines in the intestinal phase. In addition, it was determined whether the treatment with RTX affects the infectivity of T. spiralis-L1 and the development of the T. spiralis life cycle. Our results show that RTX decreased serum levels of IL-12, INF-γ, IL-1β, TNF-α and parasite burden on muscle tissue. It was observed that T. spiralis-L1 treated with RTX decreased their infectivity affecting the development of the T. spiralis life cycle in mouse. These results demonstrate that RTX is able to inhibit the production of Th1 cytokines, contributing to the defence against T. spiralis, which places it as a potential drug modulator of the immune response.