Frontiers in Immunology (Aug 2021)

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

  • Emma N. Goddery,
  • Emma N. Goddery,
  • Cori E. Fain,
  • Cori E. Fain,
  • Chloe G. Lipovsky,
  • Chloe G. Lipovsky,
  • Katayoun Ayasoufi,
  • Lila T. Yokanovich,
  • Lila T. Yokanovich,
  • Courtney S. Malo,
  • Courtney S. Malo,
  • Roman H. Khadka,
  • Roman H. Khadka,
  • Zachariah P. Tritz,
  • Zachariah P. Tritz,
  • Fang Jin,
  • Michael J. Hansen,
  • Aaron J. Johnson,
  • Aaron J. Johnson,
  • Aaron J. Johnson

DOI
https://doi.org/10.3389/fimmu.2021.726421
Journal volume & issue
Vol. 12

Abstract

Read online

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-2Kb and H-2Db upon infection. Conditional ablation of H-2Kb and H-2Db from CNS-myeloid cells allowed us to determine that antigen presentation via H-2Db, but not H-2Kb, 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.

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