Human intestinal lymphocytes, particularly intraepithelial lymphocytes
, proliferate minimally to some agents, like mitogens and stimuli of t
he CD3 pathway. This in vitro finding may be due, in part, to a loss o
f factors found in vivo. Three T-cell growth factors, IL-7, IL-9, and
IL-12, were tested for their ability to stimulate the proliferation of
intestinal lymphocytes. Both intraepithelial lymphocytes and lamina p
ropria lymphocytes proliferated more vigorously to IL-7 than to IL-9 o
r IL-12, and only IL-7 increased stimulation through the CD3 pathway.
The IL-7-induced response was IL-2-dependent: IL-2 receptors appeared
on both intestinal lymphocyte types, and antibody to the IL-2 receptor
blocked IL-7-induced proliferation. Both CD4(+) and CD8(+) T-cell sub
sets responded to this cytokine as shown by phenotype-depletion experi
ments and constancy in the CD4/CD8 ratios after culture with IL-7. In
addition, the T-cell receptor alpha beta and gamma delta subsets respo
nded equally well to IL-7. This newly described selective proliferativ
e response of intestinal lymphocytes to IL-7, but not to IL-9 or IL-12
, requires no preactivation and may enhance growth in vivo.