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Vanilloid Receptor 1 Agonists, Capsaicin and Resiniferatoxin, Enhance MHC Class I-restricted Viral Antigen Presentation in Virus-infected Dendritic Cells
Immune Network ; : 233-241, 2016.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-97831
Biblioteca responsável: WPRO
ABSTRACT
DCs, like the sensory neurons, express vanilloid receptor 1 (VR1). Here we demonstrate that the VR1 agonists, capsaicin (CP) and resiniferatoxin (RTX), enhance antiviral CTL responses by increasing MHC class I-restricted viral antigen presentation in dendritic cells (DCs). Bone marrow-derived DCs (BM-DCs) were infected with a recombinant vaccinia virus (VV) expressing OVA (VV-OVA), and then treated with CP or RTX. Both CP and RTX increased MHC class I-restricted presentation of virus-encoded endogenous OVA in BM-DCs. Oral administration of CP or RTX significantly increased MHC class I-restricted OVA presentation by splenic and lymph node DCs in VV-OVA-infected mice, as assessed by directly measuring OVA peptide SIINFEKL-Kb complexes on the cell surface and by performing functional assays using OVA-specific CD8 T cells. Accordingly, oral administration of CP or RTX elicited potent OVA-specific CTL activity in VV-OVA-infected mice. The results from this study demonstrate that VR1 agonists enhance anti-viral CTL responses, as well as a neuro-immune connection in anti-viral immune responses.
Assuntos

Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Óvulo / Células Receptoras Sensoriais / Vaccinia virus / Células Dendríticas / Capsaicina / Linfócitos T / Administração Oral / Apresentação de Antígeno / Linfonodos Limite: Animais Idioma: Inglês Revista: Immune Network Ano de publicação: 2016 Tipo de documento: Artigo
Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Óvulo / Células Receptoras Sensoriais / Vaccinia virus / Células Dendríticas / Capsaicina / Linfócitos T / Administração Oral / Apresentação de Antígeno / Linfonodos Limite: Animais Idioma: Inglês Revista: Immune Network Ano de publicação: 2016 Tipo de documento: Artigo
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