4.6 Article

PTPN22 Alters the Development of Regulatory T Cells in the Thymus

Journal

JOURNAL OF IMMUNOLOGY
Volume 188, Issue 11, Pages 5267-5275

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1200150

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Funding

  1. National Institutes of Health [AI070351, AI050864, 5R01AI070544]
  2. Juvenile Diabetes Research Foundation
  3. Wellcome Trust [079895]

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PTPN22 encodes a tyrosine phosphatase that inhibits Src-family kinases responsible for Ag receptor signaling in lymphocytes and is strongly linked with susceptibility to a number of autoimmune diseases. As strength of TCR signal is critical to the thymic selection of regulatory T cells (Tregs), we examined the effect of murine PTPN22 deficiency on Treg development and function. In the thymus, numbers of pre-Tregs and Tregs increased inversely with the level of PTPN22. This increase in Tregs persisted in the periphery and could play a key part in the reduced severity observed in the PTPN22-deficient mice of experimental autoimmune encephalomyelitis, a mouse model of multiple sclerosis. This could explain the lack of association of certain autoimmune conditions with PTPN22 risk alleles. The Journal of Immunology, 2012, 188: 5267-5275.

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