4.6 Article

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

期刊

JOURNAL OF IMMUNOLOGY
卷 191, 期 9, 页码 4581-4588

出版社

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1300439

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  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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