Journal
JOURNAL OF INFECTIOUS DISEASES
Volume 205, Issue 2, Pages 320-332Publisher
OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jir734
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Funding
- Karolinska Institute
- Swedish International Development Agency
- Wellcome Trust [WT089992MA]
- US NIH Fogerty [1R21NS064888-01A1]
- Swedish Research Council
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Methods. The role of innate immune responses in the penetration of T cells and Trypanosoma brucei brucei into the brain was studied in knockout mice by using double immunofluorescent staining and real-time polymerase chain reaction. Results. We demonstrate that Toll-like receptor (TLR)-MyD88-mediated signaling is required for T-cell and parasite penetration into the brain and microglial activation, besides controlling parasitemia and antigen-specific T-cell activation. Among different TLR-deficient mice studied, TLR9 mediated parasitemia control and T-cell penetration into the brain. TLR-MyD88 signals increased levels of interferon (IFN) beta and tumor necrosis factor (TNF) alpha transcripts in the brains of infected mice and both TNF-alpha and IFN-alpha/beta, receptors promoted T-cell and trypanosoma infiltration into the brain parenchyma. Both resident and infiltrating inflammatory cells in the brain controlled parasite densities in a TLR2- and TLR9-MyD88-mediated manner. However, neither IFN-alpha/beta nor TNF-alpha contributed to parasite control in the brain. Conclusions. Our data indicate that innate immune TLR signals stimulate the expression of TNF-alpha and IFN-alpha/beta that initiate brain invasion of T cells and trypanosomes, and control T. brucei brucei load in the brain by molecules distinct from these.
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