CD70 Inversely Regulates Regulatory T Cells and Invariant NKT Cells and Modulates Type 1 Diabetes in NOD Mice

J Immunol. 2020 Oct 1;205(7):1763-1777. doi: 10.4049/jimmunol.2000148. Epub 2020 Aug 31.

Abstract

The CD27-CD70 costimulatory pathway is essential for the full activation of T cells, but some studies show that blocking this pathway exacerbates certain autoimmune disorders. In this study, we report on the impact of CD27-CD70 signaling on disease progression in the NOD mouse model of type 1 diabetes (T1D). Specifically, our data demonstrate that CD70 ablation alters thymocyte selection and increases circulating T cell levels. CD27 signaling was particularly important for the thymic development and peripheral homeostasis of Foxp3+Helios+ regulatory T cells, which likely accounts for our finding that CD70-deficient NOD mice develop more-aggressive T1D onset. Interestingly, we found that CD27 signaling suppresses the thymic development and effector functions of T1D-protective invariant NKT cells. Thus, rather than providing costimulatory signals, the CD27-CD70 axis may represent a coinhibitory pathway for this immunoregulatory T cell population. Moreover, we showed that a CD27 agonist Ab reversed the effects of CD70 ablation, indicating that the phenotypes observed in CD70-deficient mice were likely due to a lack of CD27 signaling. Collectively, our results demonstrate that the CD27-CD70 costimulatory pathway regulates the differentiation program of multiple T cell subsets involved in T1D development and may be subject to therapeutic targeting.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD27 Ligand / genetics
  • CD27 Ligand / metabolism*
  • Cell Differentiation
  • DNA-Binding Proteins / metabolism
  • Diabetes Mellitus, Type 1 / immunology*
  • Disease Models, Animal
  • Forkhead Transcription Factors / metabolism
  • Humans
  • Immunomodulation
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred NOD
  • Mice, Knockout
  • Natural Killer T-Cells / immunology*
  • Signal Transduction
  • T-Lymphocytes, Regulatory / immunology*
  • Transcription Factors / metabolism
  • Tumor Necrosis Factor Receptor Superfamily, Member 7 / metabolism

Substances

  • CD27 Ligand
  • DNA-Binding Proteins
  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • Transcription Factors
  • Tumor Necrosis Factor Receptor Superfamily, Member 7
  • Zfpn1a2 protein, mouse