Title of article :
Stable form of galectin-9, a Tim-3 ligand, inhibits contact hypersensitivity and psoriatic reactions: A potent therapeutic tool for Th1- and/or Th17-mediated skin inflammation
Author/Authors :
Niwa، نويسنده , , Haruna and Satoh، نويسنده , , Takahiro and Matsushima، نويسنده , , Yuki and Hosoya، نويسنده , , Kazuki and Saeki، نويسنده , , Kazumi and Niki، نويسنده , , Toshiro and Hirashima، نويسنده , , Mitsuomi and Yokozeki، نويسنده , , Hiroo، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2009
Abstract :
Tim-3 is a cell surface molecule preferentially expressed in Th1 and Th17 cells. Galectin-9 is a ligand for Tim-3 and the binding of galectin-9 to Tim-3 induces apoptosis. We recently developed a stable form of galectin-9 (sGal-9) by partial deletion of the linker peptide. In this study, we characterized the therapeutic effects of sGal-9 on inflammatory reactions in contact hypersensitivity and IL-23-induced psoriatic mouse models. In contact hypersensitivity in mice, the ear swelling response was suppressed by sGal-9. In vitro treatment with sGal-9 resulted in cell apoptosis of CD4, CD8, and hepatic NK cells. sGal-9-treated mice had decreased IFN-γ- and IL-17-producing T cells. Similarly, sGal-9 reduced epidermal thickness and dermal cellular infiltrate levels in IL-23-induced psoriasis-like skin inflammation. This was accompanied by decreased skin lesion levels of IL-17 and IL-22. sGal-9 may be a unique and useful therapeutic tool for the treatment of Th1- and/or Th17-mediated skin inflammation.
Keywords :
contact hypersensitivity , apoptosis , Galectin-9 , Th17 , psoriasis , TIM-3 , Regulatory T cells
Journal title :
Clinical Immunology
Journal title :
Clinical Immunology