The role of IL-4, -6 and -7 in the survival of T lymphocytes was studied in
vivo. The decay of polyclonal populations of CD4(+) and CD8(+) T cells was
monitored in thymectomized anti-cytokine receptor mab-treated and/or cytok
ine-deficient mice. The lack of IL-4 or -6 did not have any detectable effe
ct on T cell survival, but IL-7 played an important role in the survival of
the naive T cell compartment, especially of naive CD4(+) T cells.