IL-23 drives a pathogenic T cell population that induces autoimmune inflammation |
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| Authors: | Langrish Claire L Chen Yi Blumenschein Wendy M Mattson Jeanine Basham Beth Sedgwick Jonathan D McClanahan Terrill Kastelein Robert A Cua Daniel J |
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| Affiliation: | Discovery Research, DNAX Research Inc., Palo Alto, CA 94304, USA. |
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| Abstract: | Interleukin (IL)-23 is a heterodimeric cytokine composed of a unique p19 subunit, and a common p40 subunit shared with IL-12. IL-12 is important for the development of T helper (Th)1 cells that are essential for host defense and tumor suppression. In contrast, IL-23 does not promote the development of interferon-gamma-producing Th1 cells, but is one of the essential factors required for the expansion of a pathogenic CD4(+) T cell population, which is characterized by the production of IL-17, IL-17F, IL-6, and tumor necrosis factor. Gene expression analysis of IL-23-driven autoreactive T cells identified a unique expression pattern of proinflammatory cytokines and other novel factors, distinguishing them from IL-12-driven T cells. Using passive transfer studies, we confirm that these IL-23-dependent CD4(+) T cells are highly pathogenic and essential for the establishment of organ-specific inflammation associated with central nervous system autoimmunity. |
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