Upon antigenic stimulation, naive T lymphocytes proliferate and a fraction
of the activated cells acquire a T helper cell type 1 (Th1) or Th2 phenotyp
e as well as the capacity to migrate to inflamed tissues. However, the anti
gen-primed T cells that receive a short T cell receptor (TCR) stimulation d
o not acquire effector function and remain in a nonpolarized state. Using T
CR transgenic CD4(+) T cells in an adoptive transfer system, we compared th
e in vivo migratory capacities of naive, nonpolarized, Th1 or Th2 cells. Al
though all cell types migrated to the spleen, only naive and nonpolarized T
cells efficiently migrated to lymph nodes. In addition Th1, but not Th2, m
igrated to inflamed tissues. In the lymph nodes, nonpolarized T cells proli
ferated and acquired effector function in response to antigenic stimulation
, displaying lower activation threshold and faster kinetics compared with n
aive T cells. These results suggest that nonpolarized T cells are in an int
ermediate state of differentiation characterized by lymph node homing capac
ity and increased responsiveness that allows them to mount a prompt and eff
ective secondary response.