Tolerogenic nanoparticles suppress central nervous system inflammation

Proc Natl Acad Sci U S A. 2020 Dec 15;117(50):32017-32028. doi: 10.1073/pnas.2016451117. Epub 2020 Nov 25.


Therapeutic approaches for the induction of immune tolerance remain an unmet clinical need for the treatment of autoimmune diseases, including multiple sclerosis (MS). Based on its role in the control of the immune response, the ligand-activated transcription factor aryl hydrocarbon receptor (AhR) is a candidate target for novel immunotherapies. Here, we report the development of AhR-activating nanoliposomes (NLPs) to induce antigen-specific tolerance. NLPs loaded with the AhR agonist ITE and a T cell epitope from myelin oligodendrocyte glycoprotein (MOG)35-55 induced tolerogenic dendritic cells and suppressed the development of experimental autoimmune encephalomyelitis (EAE), a preclinical model of MS, in preventive and therapeutic setups. EAE suppression was associated with the expansion of MOG35-55-specific FoxP3+ regulatory T cells (Treg cells) and type 1 regulatory T cells (Tr1 cells), concomitant with a reduction in central nervous system-infiltrating effector T cells (Teff cells). Notably, NLPs induced bystander suppression in the EAE model established in C57BL/6 × SJL F1 mice. Moreover, NLPs ameliorated chronic progressive EAE in nonobese diabetic mice, a model which resembles some aspects of secondary progressive MS. In summary, these studies describe a platform for the therapeutic induction of antigen-specific tolerance in autoimmune diseases.

Keywords: EAE; MS; antigen-specific therapy; autoimmunity; nanoparticles.

MeSH terms

  • Animals
  • Bystander Effect / drug effects
  • Bystander Effect / immunology
  • Drug Combinations
  • Encephalomyelitis, Autoimmune, Experimental / drug therapy*
  • Encephalomyelitis, Autoimmune, Experimental / immunology
  • Epitopes, T-Lymphocyte / immunology
  • Female
  • Humans
  • Immune Tolerance / drug effects*
  • Immunosuppressive Agents / administration & dosage*
  • Immunosuppressive Agents / immunology
  • Indoles / administration & dosage
  • Indoles / immunology
  • Liposomes
  • Mice
  • Multiple Sclerosis / drug therapy*
  • Multiple Sclerosis / immunology
  • Myelin-Oligodendrocyte Glycoprotein / administration & dosage
  • Myelin-Oligodendrocyte Glycoprotein / immunology
  • Nanoparticles / chemistry
  • Peptide Fragments / administration & dosage
  • Peptide Fragments / immunology
  • Receptors, Aryl Hydrocarbon / agonists
  • Receptors, Aryl Hydrocarbon / metabolism
  • Signal Transduction / drug effects
  • Signal Transduction / immunology
  • T-Lymphocytes, Regulatory / immunology
  • Thiazoles / administration & dosage
  • Thiazoles / immunology


  • 2-(1'H-indole-3'-carbonyl)thiazole-4-carboxylic acid methyl ester
  • Drug Combinations
  • Epitopes, T-Lymphocyte
  • Immunosuppressive Agents
  • Indoles
  • Liposomes
  • Myelin-Oligodendrocyte Glycoprotein
  • Peptide Fragments
  • Receptors, Aryl Hydrocarbon
  • Thiazoles
  • myelin oligodendrocyte glycoprotein (35-55)