Decreased production of IL-2 and IFN-γ by stimulated splenocytes from mice bearing plasma cell tumors is associated with alteration of DNA-binding factors

: We have previously demonstrated that polyclonally stimulated splenocytes as well as enriched T cells from mice bearing plasma cell tumors (PCT) show decreased production of the Th1-associated cytokines, IL-2 and IFN-gamma. This observed loss of IL-2 and IFN-gamma production could be attributed to possible alterations in various factors required for T cell activation and cytokine production. We find that B7 co-stimulatory molecules and IL-2R are up-regulated normally on splenocytes from PCT mice. Concanavalin A (Con A) stimulation of splenocytes from PCT mice in the presence of immobilized anti-CD28 antibody does not enhance proliferation. Exogenous rIL-2 addition to cultures of splenocytes from PCT mice also does not enhance proliferative responses or cytokine production. Furthermore, we do not observe inhibition of normal splenocyte proliferation and IL-2 production in the presence of splenocytes from PCT mice, suggesting that the appearance of suppressor cells cannot account for the decreased responses by splenocytes from PCT mice. Also, IL-2 mRNA levels are decreased in stimulated splenocytes from PCT mice, suggesting that there may be an alteration of transcription factors required for activation of IL-2. Therefore, we have evaluated the DNA-binding activity of transcription factors involved in activation of IL-2 and IFN-gamma gene transcription. We find that binding activities of AP-1, Oct-1 and Oct-2 transcription factors in stimulated splenocytes from PCT mice are similar to normal splenocytes. However, the binding activities of NF-kappa B complexes and factors that bind to the proximal conserved element in the IFN-gamma promoter are dramatically altered in splenocytes from PCT mice. These results suggest that PCT induce changes in certain transcription factors that are important for anti-tumor responses, including T cell proliferative responses and Th1-associated cytokine production.