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Human regulatory T cells in autoimmune diseases

Journal

CURRENT OPINION IN IMMUNOLOGY
Volume 22, Issue 6, Pages 753-760

Publisher

CURRENT BIOLOGY LTD
DOI: 10.1016/j.coi.2010.08.012

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Funding

  1. National Institutes of Health [P01 AI045757, U19 AI046130, U19 AI070352, P01 AI039671]
  2. National Institute of Neurological Disorders and Stroke [NS2427]
  3. Howard Hughes Medical Institute

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Human regulatory T cells (Tregs) play a critical role in preventing autoimmunity, and their failure contributes to autoimmune diseases. In recent years, our understanding of human Tregs has been greatly enhanced by improvements in the definition and isolation of pure human Tregs, as well as by the discovery of phenotypically and functionally distinct human Treg subsets. This progress has also yielded a better understanding of the mechanisms of human Treg suppression and the role of human Tregs in autoimmune diseases. An unexpected discovery is that human Tregs have considerable plasticity that allows them to produce the pro-inflammatory cytokine IL-17 under certain conditions. These recent advances highlight the importance of studying the roles of both mouse and human Tregs in autoimmunity.

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