C1858T Polymorphism of Protein Tyrosine Phosphatase Non-receptor Type 22 (PTPN22): an eligible target for prevention of type 1 diabetes?

Expert Rev Clin Immunol. 2017 Mar;13(3):189-196. doi: 10.1080/1744666X.2017.1266257. Epub 2016 Dec 8.

Abstract

In type 1 diabetes (T1D), several genetic factors are associated to β-cell autoimmunity onset and clinical progression. HLA-genes play a major role in susceptibility and initiation of β-cell autoimmunity, whereas non-HLA genes may influence the destruction rate. Areas covered: Our review focuses on the possible role of the PTPN22 C1858 T variant as a prognostic factor, given its influence on disease variability. Moreover, we present the potential role of C1858 T as a target for tertiary prevention trials and new therapeutic strategies, such as the LYP inhibitors. We used PubMed for literature research; key words were 'PTPN22', 'C1858 T polymorphism', 'lymphoid-specific tyrosine phosphatase' and 'type 1 diabetes'. We selected publications between 2000 and 2016. Expert commentary: Current data suggest that PTPN22 can be a promising target for therapeutic interventions and identification of at-risk subjects in autoimmune diseases such as T1D.

Keywords: Ptpn22; autoantibodies; autoimmune diseases; experimental pharmacology; lyp protein; polimorphism; prevention; type 1 diabetes.

Publication types

  • Review

MeSH terms

  • Animals
  • Clinical Trials as Topic
  • Diabetes Mellitus, Type 1 / drug therapy
  • Diabetes Mellitus, Type 1 / genetics*
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Hypoglycemic Agents / therapeutic use*
  • Molecular Targeted Therapy
  • Polymorphism, Genetic
  • Protein Tyrosine Phosphatase, Non-Receptor Type 22 / antagonists & inhibitors
  • Protein Tyrosine Phosphatase, Non-Receptor Type 22 / genetics*

Substances

  • Hypoglycemic Agents
  • PTPN22 protein, human
  • Protein Tyrosine Phosphatase, Non-Receptor Type 22