TRANSPLANTATION SOCS3 regulates graft-versus-host disease

نویسندگان

  • Geoffrey R. Hill
  • Rachel D. Kuns
  • Neil C. Raffelt
  • Alistair L. J. Don
  • Stuart D. Olver
  • Kate A. Markey
  • Yana A. Wilson
  • Joel Tocker
  • Warren S. Alexander
  • Andrew D. Clouston
  • Andrew W. Roberts
  • Kelli P. A. MacDonald
چکیده

Suppressor of cytokine signaling-3 (SOCS3) is the main intracellular regulator of signaling by granulocyte colony-stimulating factor, an immune-modulatory cytokine used to mobilize stem cells for transplantation. We have therefore studied the contribution of SOCS3 to the spectrum of graft-versus-host disease (GVHD) after allogeneic stem cell transplantation (SCT). Grafts from SOCS3 / vav donor mice in which SOCS3 deficiency is restricted to the hematopoietic compartment had an augmented capacity to induce acute GVHD. With the use of SOCS3 / LysM and SOCS3 / lck donors in which SOCS3 deficiency was restricted to the myeloid or T-cell lineage, respectively, we confirmed SOCS3 deficiency promoted acute GVHD mortality and histopathology within the gastrointestinal tract by effects solely within the donor T cell. SOCS3 / lck donor T cells underwent enhanced alloantigendependent proliferation and generation of interleukin-10 (IL-10), IL-17, and interferon(IFN ) after SCT. The enhanced capacity of the SOCS3 / lck donor T cell to induce acute GVHD was dependent on IFN but independent of IL-10 or IL-17. Surprisingly, SOCS3 / lck donor T cells also induced severe, transforming growth factor – and IFN -dependent, sclerodermatous GVHD. Thus, the delivery of small molecule SOCS3 mimetics may prove to be useful for the inhibition of both acute and chronic GVHD. (Blood. 2010;116(2): 287-296)

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تاریخ انتشار 2010