Skin-derived TSLP systemically expands regulatory T cells

Theresa M. Leichner, Atsushi Satake, Victor Sanoe Harrison, Yukinori Tanaka, Angela S. Archambault, Brian S. Kim, Mark C. Siracusa, Warren J. Leonard, Ali Naji, Gregory F. Wu, David Artis, Taku Kambayashi

Research output: Contribution to journalArticlepeer-review

24 Citations (Scopus)


Regulatory T cells (Tregs) are a subset of CD4+ T cells with suppressive function and are critical for limiting inappropriate activation of T cells. Hence, the expansion of Tregs is an attractive strategy for the treatment of autoimmune diseases. Here, we demonstrate that the skin possesses the remarkable capacity to systemically expand Treg numbers by producing thymic stromal lymphopoietin (TSLP) in response to vitamin D receptor stimulation. An ∼2-fold increase in the proportion and absolute number of Tregs was observed in mice treated topically but not systemically with the Vitamin D3 analog MC903. This expansion of Tregs was dependent on TSLP receptor signaling but not on VDR signaling in hematopoietic cells. However, TSLP receptor expression by Tregs was not required for their proliferation. Rather, skin-derived TSLP promoted Treg expansion through dendritic cells. Importantly, treatment of skin with MC903 significantly lowered the incidence of autoimmune diabetes in non-obese diabetic mice and attenuated disease score in experimental autoimmune encephalomyelitis. Together, these data demonstrate that the skin has the remarkable potential to control systemic immune responses and that Vitamin D-mediated stimulation of skin could serve as a novel strategy to therapeutically modulate the systemic immune system for the treatment of autoimmunity.

Original languageEnglish
Pages (from-to)39-52
Number of pages14
JournalJournal of Autoimmunity
Publication statusPublished - 2017 May 1


  • Immunotherapy
  • Regulatory T cells
  • Thymic stromal lymphopoietin
  • Tolerance
  • Vitamin D


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