TY - JOUR
T1 - Meningeal macrophages protect against viral neuroinfection
AU - Rebejac, Julie
AU - Eme-Scolan, Elisa
AU - Arnaud Paroutaud, Laurie
AU - Kharbouche, Sarah
AU - Teleman, Matei
AU - Spinelli, Lionel
AU - Gallo, Emeline
AU - Roussel-Queval, Annie
AU - Zarubica, Ana
AU - Sansoni, Amandine
AU - Bardin, Quentin
AU - Hoest, Philippe
AU - Michallet, Marie Cécile
AU - Brousse, Carine
AU - Crozat, Karine
AU - Manglani, Monica
AU - Liu, Zhaoyuan
AU - Ginhoux, Florent
AU - McGavern, Dorian B.
AU - Dalod, Marc
AU - Malissen, Bernard
AU - Lawrence, Toby
AU - Rua, Rejane
N1 - Publisher Copyright:
© 2022 Elsevier Inc.
PY - 2022/11/8
Y1 - 2022/11/8
N2 - The surface of the central nervous system (CNS) is protected by the meninges, which contain a dense network of meningeal macrophages (MMs). Here, we examined the role of tissue-resident MM in viral infection. MHC-II− MM were abundant neonatally, whereas MHC-II+ MM appeared over time. These barrier macrophages differentially responded to in vivo peripheral challenges such as LPS, SARS-CoV-2, and lymphocytic choriomeningitis virus (LCMV). Peripheral LCMV infection, which was asymptomatic, led to a transient infection and activation of the meninges. Mice lacking macrophages but conserving brain microglia, or mice bearing macrophage-specific deletion of Stat1 or Ifnar, exhibited extensive viral spread into the CNS. Transcranial pharmacological depletion strategies targeting MM locally resulted in several areas of the meninges becoming infected and fatal meningitis. Low numbers of MHC-II+ MM, which is seen upon LPS challenge or in neonates, corelated with higher viral load upon infection. Thus, MMs protect against viral infection and may present targets for therapeutic manipulation.
AB - The surface of the central nervous system (CNS) is protected by the meninges, which contain a dense network of meningeal macrophages (MMs). Here, we examined the role of tissue-resident MM in viral infection. MHC-II− MM were abundant neonatally, whereas MHC-II+ MM appeared over time. These barrier macrophages differentially responded to in vivo peripheral challenges such as LPS, SARS-CoV-2, and lymphocytic choriomeningitis virus (LCMV). Peripheral LCMV infection, which was asymptomatic, led to a transient infection and activation of the meninges. Mice lacking macrophages but conserving brain microglia, or mice bearing macrophage-specific deletion of Stat1 or Ifnar, exhibited extensive viral spread into the CNS. Transcranial pharmacological depletion strategies targeting MM locally resulted in several areas of the meninges becoming infected and fatal meningitis. Low numbers of MHC-II+ MM, which is seen upon LPS challenge or in neonates, corelated with higher viral load upon infection. Thus, MMs protect against viral infection and may present targets for therapeutic manipulation.
KW - LCMV
KW - brain
KW - immunological barrier
KW - interferon
KW - macrophages
KW - meninges
KW - neuroinfection
KW - virus
UR - http://www.scopus.com/inward/record.url?scp=85141324006&partnerID=8YFLogxK
U2 - 10.1016/j.immuni.2022.10.005
DO - 10.1016/j.immuni.2022.10.005
M3 - Article
C2 - 36323311
AN - SCOPUS:85141324006
SN - 1074-7613
VL - 55
SP - 2103-2117.e10
JO - Immunity
JF - Immunity
IS - 11
ER -