Zinc deficiency is accompanied by a severe impairment of the immune system, causing a high risk for
infections and
autoimmune diseases due to altered functionality of B- and T- cells. The influence of
zinc deficiency on T- and B- cells via alteration of
cytokine expression is well established. The aim of this study was to examine potential direct effects of
zinc deficiency on the reactivity of B- and T- cells.
Zinc deficient B- and T- cells revealed divergent reaction patterns compared to
zinc sufficienT-cells. This was manifested by a stronger proliferative response following
IL-6 and
IL-2 stimulation on the one hand, but less proliferation following
IL-4 stimulation on the other hand. Moreover, these results were supported by the finding that the B- and T-cell signaling cascades activated by
IL-4 or
IL-6, respectively, were affected directly by
zinc deficiency, resulting in reduced Stat6 phosphorylation and increased Stat3 phosphorylation. Whereas the
transcription factor Stat6 is involved in
IL-4 signaling, Stat3 is activated by
IL-6 signaling. Consequently, these results show opposing effects of
zinc deficiency on
IL-4 and IL-6/IL-2 signaling pathways, thus underlying the importance of
zinc for proper immune function.