Abstract
We investigated the role of IL-12 in regulating IL-2 and IFN-γ production in primary culture of human T cells. Addition of neutralizing antiserum against the 40-kDa subunit of IL-12 to PHA-stimulated PBMC markedly reduced both IFN-γ protein production and mRNA accumulation and stability. Moreover, concurrent treatment of partially purified T cells (>90% CD3+) with PHA and rlL-12 selectively enhanced IFN-γ mRNA stability and protein production, while IL-2 protein and mRNA levels were unaffected. These studies also show that IFN-γ and IL-2 mRNA stability are temporally dissociated during the course of T cell activation, and we propose that this dissociation may be mediated through the production of IL-12. The effect of IL-12 on modulation of IFN-γ mRNA turnover is not associated with detectable changes in either the levels or affinity of cytoplasmic RNA-binding proteins capable of recognizing AU-rich sequences in the 3' UTR of IFN-γ mRNA.
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