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Publication : RORγt-specific transcriptional interactomic inhibition suppresses autoimmunity associated with TH17 cells.

First Author  Park TY Year  2014
Journal  Proc Natl Acad Sci U S A Volume  111
Issue  52 Pages  18673-8
PubMed ID  25527718 Mgi Jnum  J:216925
Mgi Id  MGI:5610045 Doi  10.1073/pnas.1413687112
Citation  Park TY, et al. (2014) RORgammat-specific transcriptional interactomic inhibition suppresses autoimmunity associated with TH17 cells. Proc Natl Acad Sci U S A 111(52):18673-8
abstractText  The nuclear hormone receptor retinoic acid-related orphan receptor gamma t (RORgammat) is a transcription factor (TF) specific to TH17 cells that produce interleukin (IL)-17 and have been implicated in a wide range of autoimmunity. Here, we developed a novel therapeutic strategy to modulate the functions of RORgammat using cell-transducible form of transcription modulation domain of RORgammat (tRORgammat-TMD), which can be delivered effectively into the nucleus of cells and into the central nerve system (CNS). tRORgammat-TMD specifically inhibited TH17-related cytokines induced by RORgammat, thereby suppressing the differentiation of naive T cells into TH17, but not into TH1, TH2, or Treg cells. tRORgammat-TMD injected into experimental autoimmune encephalomyelitis (EAE) animal model can be delivered effectively in the splenic CD4(+) T cells and spinal cord-infiltrating CD4(+) T cells, and suppress the functions of TH17 cells. The clinical severity and incidence of EAE were ameliorated by tRORgammat-TMD in preventive and therapeutic manner, and significant reduction of both infiltrating CD4(+) IL-17(+) T cells and inflammatory cells into the CNS was observed. As a result, the number of spinal cord demyelination was also reduced after tRORgammat-TMD treatment. With the same proof of concept, tTbet-TMD specifically blocking TH1 differentiation improved the clinical incidence of rheumatoid arthritis (RA). Therefore, tRORgammat-TMD and tTbet-TMD can be novel therapeutic reagents with the natural specificity for the treatment of inflammatory diseases associated with TH17 or TH1. This strategy can be applied to treat various diseases where a specific transcription factor has a key role in pathogenesis.
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