CD8+ cytotoxic T lymphocytes (CTL) have an established role in anti-vi
ral immunity, but whether CTL function efficiently in the brain remain
s unclear. In particular, virus-infected neurons, which express only l
ow levels of MHC class I antigens and are resistant to the induction o
f apoptosis, could constitute a relatively intractable CTL target. we
have used immune lymphocytes adoptively transferred into the CSF to pr
otect naive mice against an intracerebral infection with influenza A/W
SN, a virus that infects neurons in the brain parenchyma and causes a
lethal encephalitis. After in vitro restimulation, heterotypically imm
une spleen cells protected against A/WSN encephalitis in an H-2-restri
cted, CD8-dependent, CD4-independent manner. Adoptively transferred CT
L clones were also protective. Homotypically immune spleen cells addit
ionally mediated CD8-independent, H-P-unrestricted protection, probabl
y due to the generation of A/WSN-specific plasma cells from memory B c
ells during in vitro restimulation. Thus after in vitro restimulation,
either CTL or B cells adoptively transferred into the CSF protected a
gainst an acutely lethal intracerebral virus infection. (C) 1997 Acade
mic Press.