Antibody blockade of IL-15 signaling has the potential to durably reverse vitiligo

Jillian M. Richmond, James P. Strassner, Lucio Z. Zapata, Madhuri Garg, Rebecca L. Riding, Maggi A. Refat, Xueli Fan, Vincent Azzolino, Andrea Tovar-Garza, Naoya Tsurushita, Amit G. Pandya, J. Yun Tso, John E. Harris

Research output: Contribution to journalArticlepeer-review

146 Scopus citations


Vitiligo is an autoimmune disease of the skin mediated by CD8+ T cells that kill melanocytes and create white spots. Skin lesions in vitiligo frequently return after discontinuing conventional treatments, supporting the hypothesis that autoimmune memory is formed at these locations. We found that lesional T cells in mice and humans with vitiligo display a resident memory (TRM) phenotype, similar to those that provide rapid, localized protection against reinfection from skin and mucosal-tropic viruses. Interleukin-15 (IL-15)-deficient mice reportedly have impaired TRM formation, and IL-15 promotes TRM function ex vivo. We found that both human and mouse TRM express the CD122 subunit of the IL-15 receptor and that keratinocytes up-regulate CD215, the subunit required to display the cytokine on their surface to promote activation of T cells. Targeting IL-15 signaling with an anti-CD122 antibody reverses disease in mice with established vitiligo. Short-term treatment with anti-CD122 inhibits TRM production of interferon- (IFN), and long-term treatment depletes TRM from skin lesions. Short-term treatment with anti-CD122 can provide durable repigmentation when administered either systemically or locally in the skin.

Original languageEnglish (US)
Article numbereaam7710
JournalScience translational medicine
Issue number450
StatePublished - Jul 18 2018

ASJC Scopus subject areas

  • General Medicine


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