An altered CD8+ T cell epitope of insulin prevents type 1 diabetes in humanized NOD mice

Cell Mol Immunol. 2019 Jun;16(6):590-601. doi: 10.1038/s41423-018-0058-3. Epub 2018 Jun 28.

Abstract

Autoreactive CD8+ T cells, which play an indispensable role in β cell destruction, represent an emerging target for the prevention of type 1 diabetes (T1D). Altered peptide ligands (APLs) can efficiently induce antigen-specific T cells anergy, apoptosis or shifts in the immune response. Here, we found that HLA-A*0201-restricted CD8+ T cell responses against a primary β-cell autoantigen insulin epitope InsB15-14 were present in both NOD.β2mnull.HHD NOD mice and T1D patients. We generated several APL candidates for InsB15-14 by residue substitution at the p6 position. Only H6F exhibited an inhibitory effect on mInsB15-14-specific CD8+ T cell responses in vitro. H6F treatment significantly reduced the T1D incidence, which was accompanied by diminished autoreactive CD8+ T cell responses to mInsB15-14, inhibited infiltration of CD8+ and CD4+ T cells in the pancreas and reduced pro-inflammatory cytokine production in pancreatic and splenic T cells in NOD.β2mnull.HHD mice. Mechanistically, H6F treatment significantly augmented a tiny portion of CD8+CD25+Foxp3+ T cells in the spleen and especially in the pancreas. This subset exhibited typical Treg phenotypes and required peptide-specific restimulation to exert immunosuppressive activity. Therefore, this APL H6F may be a promising candidate with potential clinical application value for antigen-specific prevention of T1D.

Keywords: Altered peptide ligand; CD8+CD25+Foxp3+ regulatory T cells; InsB15–14; NOD.β2m null .HHD mice; Type 1 diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Clonal Anergy
  • Diabetes Mellitus, Type 1 / immunology*
  • Diabetes Mellitus, Type 1 / therapy
  • Epitopes, T-Lymphocyte / genetics
  • Epitopes, T-Lymphocyte / immunology
  • Epitopes, T-Lymphocyte / metabolism*
  • Forkhead Transcription Factors / metabolism
  • HLA-A2 Antigen / genetics
  • Humans
  • Insulin / immunology
  • Insulin / metabolism*
  • Mice
  • Mice, Inbred NOD
  • Mutagenesis, Site-Directed
  • Pancreas / immunology*
  • Peptides / immunology
  • Peptides / metabolism*
  • T-Lymphocytes, Regulatory / immunology*

Substances

  • Epitopes, T-Lymphocyte
  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • HLA-A*02:01 antigen
  • HLA-A2 Antigen
  • Insulin
  • Peptides