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Cell Rep ; 27(11): 3254-3268.e8, 2019 06 11.
Article in English | MEDLINE | ID: mdl-31189109

ABSTRACT

Control of CNS pathogens by CD8 T cells is key to avoid fatal neuroinflammation. Yet, the modalities of MHC I presentation in the brain are poorly understood. Here, we analyze the antigen presentation mechanisms underlying CD8 T cell-mediated control of the Toxoplasma gondii parasite in the CNS. We show that MHC I presentation of an efficiently processed model antigen (GRA6-OVA), even when not expressed in the bradyzoite stage, reduces cyst burden and dampens encephalitis in C57BL/6 mice. Antigen presentation assays with infected primary neurons reveal a correlation between lower MHC I presentation of tachyzoite antigens by neurons and poor parasite control in vivo. Using conditional MHC I-deficient mice, we find that neuronal MHC I presentation is required for robust restriction of T. gondii in the CNS during chronic phase, showing the importance of MHC I presentation by CNS neurons in the control of a prevalent brain pathogen.


Subject(s)
Antibodies, Protozoan/immunology , Brain/immunology , Histocompatibility Antigens Class I/immunology , Toxoplasmosis, Cerebral/immunology , Animals , Antigens, Protozoan/immunology , Brain/cytology , Brain/parasitology , Cell Line , Cells, Cultured , Histocompatibility Antigens Class I/genetics , Humans , Male , Mice , Mice, Inbred C57BL , Neurons/immunology , Neurons/parasitology , Protozoan Proteins/immunology , Toxoplasma/immunology , Toxoplasma/pathogenicity
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