The pleiotropic cytokine IL-21 is implicated in the pathogenesis of human systemic lupus erythematosus by polymorphisms in the molecule and its receptor (IL-21R). The systemic lupus erythematosus-like autoimmune disease of BXSB.Yaa mice is critically dependent on IL-21 signaling, providing a model for understanding IL-21/IL-21R signaling in lupus pathogenesis. In this study, we generated BXSB.Yaa mice selectively deficient in IL-21R on B cells, on all T cells, or on CD8+ T cells alone and examined the effects on disease. We found that IL-21 signaling to B cells is essential for the development of all classical disease manifestations, but that IL-21 signaling also supports the expansion of central memory, CD8+ suppressor cells and broadly represses the cytokine activity of CD4+ T cells. These results indicate that IL-21 has both disease-promoting and disease-suppressive effects in the autoimmune disease of BXSB.Yaa mice.
CITATION STYLE
McPhee, C. G., Bubier, J. A., Sproule, T. J., Park, G., Steinbuck, M. P., Schott, W. H., … Roopenian, D. C. (2013). IL-21 Is a Double-Edged Sword in the Systemic Lupus Erythematosus–like Disease of BXSB. Yaa Mice. The Journal of Immunology, 191(9), 4581–4588. https://doi.org/10.4049/jimmunol.1300439
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