STAT3 is required for IL-21-induced secretion of IgE from human naive B cells
The production of IgE is tightly regulated. This is evidenced by the fact that it comprises <0.0001% of serum Ig, and aberrant production causes atopic conditions including allergy, rhinitis and anaphylaxis. IL-4 is a well-characterised inducer of IgE by human and murine B cells, while IFN-gamma can antagonise this effect. IL-21 has also been recognised for its ability to suppress IL-4-induced IgE production by murine B cells. Here, we identified IL-21 as an inducer of IgE production by CD40L-stimulated human naive B cells. Furthermore, there was a striking synergistic effect between IL-4 and IL-21 on inducing IgE secretion by all subsets of CD40L-stimulated human B cells, such that the levels detected under these conditions exceeded those induced by IL-4 or IL-21 alone by >10 fold. IL-21 induced activation of STAT3 and analysis of B cells from patients with loss-of-function STAT3 mutations revealed that the ability of IL-21 to induce IgE secretion, and augment that driven by IL-4, was STAT3-dependent. These findings highlight a fundamental difference between the regulation of IgE production by human and murine B cells and have implications for the dysregulated production of IgE in conditions characterised by extremely high levels of serum IgE.
|Authors||Avery, D. T.;Ma, C. S.;Bryant, V. L.;Santner-Nanan, B.;Nanan, R.;Wong, M.;Fulcher, D. A.;Cook, M. C.;Tangye, S. G. :|
|Published Date||2008-01-01 00:00:00|
|OpenAccess Link||https://publications.gimr.garvan.org.au/download.php?2311_10122/08 Avery Blood.pdf|