Targeting FOXP3 complex ensemble in drug discovery

Adv Protein Chem Struct Biol. 2020:121:143-168. doi: 10.1016/bs.apcsb.2019.11.010. Epub 2020 Jan 7.

Abstract

Forkhead Box P3 (FOXP3) is a key transcriptional regulator of regulatory T cells (Tregs), especially for its function of immune suppression. The special immune suppression function of Tregs plays an important role in maintaining immune homeostasis, and is related to several diseases including cancer, and autoimmune diseases. At the same time, FOXP3 takes a place in a large transcriptional complex, whose stability and functions can be controlled by various post-translational modification. More and more researches have suggested that targeting FOXP3 or its partners might be a feasible solution to immunotherapy. In this review, we focus on the transcription factor FOXP3 in Tregs, Treg functions in diseases and the FOXP3 targets.

Keywords: Drug discovery; FOXP3; Immune therapy; Post-translational modification; Treg.

Publication types

  • Review

MeSH terms

  • Acetylation / drug effects
  • Autoimmune Diseases / drug therapy*
  • Autoimmune Diseases / genetics
  • Autoimmune Diseases / immunology
  • Autoimmune Diseases / pathology
  • Drug Discovery
  • Histone Deacetylase Inhibitors / therapeutic use*
  • Homeostasis / drug effects
  • Homeostasis / genetics
  • Homeostasis / immunology
  • Humans
  • Hypersensitivity / drug therapy*
  • Hypersensitivity / genetics
  • Hypersensitivity / immunology
  • Hypersensitivity / pathology
  • Immunologic Factors / therapeutic use*
  • Neoplasms / drug therapy*
  • Neoplasms / genetics
  • Neoplasms / immunology
  • Neoplasms / pathology
  • Organ Transplantation
  • Phosphorylation / drug effects
  • Protein Domains
  • Protein Kinase Inhibitors / therapeutic use*
  • Protein Processing, Post-Translational*
  • T-Lymphocytes, Regulatory / drug effects
  • T-Lymphocytes, Regulatory / immunology
  • T-Lymphocytes, Regulatory / pathology
  • Ubiquitination / drug effects

Substances

  • Histone Deacetylase Inhibitors
  • Immunologic Factors
  • Protein Kinase Inhibitors