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. Author manuscript; available in PMC: 2017 Feb 16.
Published in final edited form as: Semin Immunopathol. 2015 Apr 22;37(3):261–270. doi: 10.1007/s00281-015-0487-3

Table 1.

Candidate antigen presenting cells for CD8+ T cells in toxoplasma-infected brain

Cell Type Description References Disease model
Neurons CD8+ T cells damage neuronal
axons in an MHC I dependent
manner in vivo
global elevation in MHC I
expression during infection
Toxoplasma cysts are
exclusively observed in neurons
[75]



[46]

[12]
EAE


cerebral
LCMV
chronic T.
gondii
Astrocytes CD8+ T cells are capable of
forming immunological
synapses with astrocytes in vivo
mice with astrocytes lacking
cytokine receptor gp130
succumb to infection
[47] [48]


[76]
adenovirus
infection

chronic T.
gondii
Microglia CD8+ T cells observed in
contact with CD11c+ cells in
brain parenchyma
Microglia first to take up
antigen during disease
progression
[15]


[77]
chronic T.
gondii

EAE
Infiltrating/Perivascular
phagocytes
CD8+ T cells observed in
contact with CD11c+ cells in
the brain parenchyma
MHC I elevated in vasculature
of brain
CD8+ T cells interact with
perivascular APCs
Perivascular MHC I dependent
proliferation of CD8+ T cells
[15]


[46]

[45] [44]

[43]
chronic T.
gondii

cerebral
LCMV
EAE

cerebral
LCMV