Effector T cells secreting type 1 and/or type 2 lymphokines (Tc1, Tc0, Tc2)
were generated in vitro from CD8(+) T cells of mice with a transgenic TCR
recognizing lymphocytic choriomeningitis virus (LCMV) glycoprotein to compa
re their effector function in vitro and in vivo, Tc1, Tc2, and Tc0 showed s
imilar Fas- and perforin-mediated cytotoxicity in vitro. Upon adoptive tran
sfer, Tc2 and Tc0 effecters were less efficient than Tc1 at controlling LCM
V or recombinant vaccinia virus expressing the LCMV glycoprotein in vivo, T
c2 and Tc0 had decreased surface VLA-4 density and deficient activation-ind
uced LFA-1/ICAM-1-dependent homotypic adhesion in vitro, Therefore, the red
uced antiviral activity in vivo of Tc2 and Tc0 compared with Tc1 is not due
to reduced cytotoxic activity or IFN-gamma secretion but may be explained
by defective homing to the target organ due to decreased expression and/or
lower activity of adhesion molecules. (C) 2000 Academic Press.