Activation of T lymphocytes is a key event for an efficient response of the
immune system. It requires the involvement of the T cell receptor antigen
as well as costimulatory molecules such as CD28. Engagement of these recept
ors through the interaction with a foreign antigen associated with major hi
stocompatibility complex molecules and CD28 counter-receptors B7.1/B7.2, re
spectively, results in a series of signaling cascades acting in synergy and
which culminate in activation of interleukin-2 gene transcription and even
tually cell proliferation. Many studies aimed at characterizing these speci
fic effector pathways have been published; however, the actual signaling mo
lecules that transduce activation signals from the cell membrane to the nuc
leus and that directly regulate interleukin-2 gene transcription are not ye
t completely defined and remain a matter of debate. In this commentary, we
have attempted to analyze the results, which are sometimes diverging if not
totally contradictory, characterizing effector pathways that possibly are
triggered during T cell activation. (C) 1998 Elsevier Science Inc.