We have observed that 8 3 T cells from Il21−/− mice produced sign

We have observed that 8.3 T cells from Il21−/− mice produced significantly less IL-2 following antigen stimulation and that this was associated with decreased Il2 mRNA expression. At least one report has alluded to the possibility that introduction of the Il21 knock-out allele might influence the expression of Il2 gene, as these genes are located only 95 kb apart on chromosome

3 [30]. Even though daily administration of IL-21 to lymphocytic choriomeningitis (LCMV)-infected Il21−/− mice for more than a week reversed the defective IL-2 production in viral antigen-specific CD8+ T cells [28], this reversal does not rule out completely the possible influence of the Il21 knock-out allele on Il2 gene expression, and further experiments EPZ-6438 datasheet are needed to resolve this issue. The addition of exogenous IL-2 could not reverse completely the defective antigen-induced proliferation of 8.3 T cells from Il21−/− mice, suggesting that either IL-21-dependent autocrine IL-2 production is necessary to achieve maximal expansion of activated CD8+ T cells, or IL-21 may also modulate the expression of molecules that influence T cell proliferation. We did not find any significant difference in the induction of CD25 between antigen-stimulated 8.3 T cells from Il21−/− and control 8.3-NOD mice (data not shown). Moreover, normal IFN-γ production and CTL activity of Il21−/−

8.3 T cells, suggesting that lack of IL-21 signalling does not impair TCR signalling pathways that promote effector functions. Consistent with this prediction, protein tyrosine phosphorylation and calcium flux response following TCR stimulation buy BMN 673 were not affected in Il21−/− 8.3 T cells (data not shown). In agreement with this, viral antigen-specific cells in control and IL-21 or IL-21Rα-deficient mice produced comparable levels of IFN-γ [28, 30]. These considerations raise the possibility that an IL-21-sufficient environment is necessary for naive CD8+ T cells to sustain full proliferation potential

in response to antigen stimulation. This requirement may be dispensable when antigen stimulation is accompanied Protein kinase N1 by potent activation of the innate immune system and induction of other inflammatory cytokines that could compensate for IL-21, and/or when the immune response is directed towards several strong immunodominant antigens. This notion is supported by the ability of Il21−/− and Il21ra−/− mice to clear acute viral infection and mount a memory response [31]. Conversely, productive CD8+ T cell activation during persisting viral infection or to a limiting autoantigen may depend upon the continuous availability of IL-21, presumably from innate immune cells, in order to clear chronic infections or to cause autoimmune pathology. Intriguingly, the addition of IL-21 alone during antigen stimulation of CD8+ T cells inhibits proliferation (Fig. 6c).

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