Cell-mediated (type-1) immunity is necessary for immune protection against
most intracellular pathogens and, when excessive, can mediate organ-specifi
c autoimmune destruction. Mice deficient in Eta-1 (also called osteopontin)
gene expression have severely impaired type-1 immunity to viral infection
[herpes simplex virus-type 1 (KOS strain)] and bacterial infection (Listeri
a monocytogenes) and do not develop sarcoid-type granulomas. Interleukin-12
(IL-12) and interferon-gamma production is diminished, and IL-10 productio
n is increased. A phosphorylation-dependent interaction between the amino-t
erminal portion of Eta-1 and its integrin receptor stimulated IL-12 express
ion, whereas a phosphorylation-independent interaction with CD44 inhibited
IL-10 expression. These findings identify Eta-1 as a key cytokine that sets
the stage for efficient type-1 immune responses through differential regul
ation of macrophage IL-12 and IL-10 cytokine expression.