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Microglia and Perivascular Macrophages Act as Antigen Presenting Cells to Promote CD8 T Cell Infiltration of the Brain

CD8 T cell infiltration of the central nervous system (CNS) is necessary for host protection but contributes to neuropathology. Antigen presenting cells (APCs) situated at CNS borders are thought to mediate T cell entry into the parenchyma during neuroinflammation. The identity of the CNS-resident A...

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Detalles Bibliográficos
Autores principales: Goddery, Emma N., Fain, Cori E., Lipovsky, Chloe G., Ayasoufi, Katayoun, Yokanovich, Lila T., Malo, Courtney S., Khadka, Roman H., Tritz, Zachariah P., Jin, Fang, Hansen, Michael J., Johnson, Aaron J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8435747/
https://www.ncbi.nlm.nih.gov/pubmed/34526998
http://dx.doi.org/10.3389/fimmu.2021.726421
Descripción
Sumario:CD8 T cell infiltration of the central nervous system (CNS) is necessary for host protection but contributes to neuropathology. Antigen presenting cells (APCs) situated at CNS borders are thought to mediate T cell entry into the parenchyma during neuroinflammation. The identity of the CNS-resident APC that presents antigen via major histocompatibility complex (MHC) class I to CD8 T cells is unknown. Herein, we characterize MHC class I expression in the naïve and virally infected brain and identify microglia and macrophages (CNS-myeloid cells) as APCs that upregulate H-2K(b) and H-2D(b) upon infection. Conditional ablation of H-2K(b) and H-2D(b) from CNS-myeloid cells allowed us to determine that antigen presentation via H-2D(b), but not H-2K(b), was required for CNS immune infiltration during Theiler’s murine encephalomyelitis virus (TMEV) infection and drives brain atrophy as a consequence of infection. These results demonstrate that CNS-myeloid cells are key APCs mediating CD8 T cell brain infiltration.