4.6 Article

IL-21 Is a Double-Edged Sword in the Systemic Lupus Erythematosus-like Disease of BXSB.Yaa Mice

Journal

JOURNAL OF IMMUNOLOGY
Volume 191, Issue 9, Pages 4581-4588

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1300439

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Funding

  1. Intramural Research Program of the National Institutes of Health, National Institute of Allergy and Infectious Diseases
  2. Alliance for Lupus Research
  3. National Institutes of Health
  4. Arthritis Foundation

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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.

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