Tryptophan metabolism promotes immune evasion in human pancreatic β cells

EBioMedicine. 2023 Sep:95:104740. doi: 10.1016/j.ebiom.2023.104740. Epub 2023 Aug 1.

Abstract

Background: To resist the autoimmune attack characteristic of type 1 diabetes, insulin producing pancreatic β cells need to evade T-cell recognition. Such escape mechanisms may be conferred by low HLA class I (HLA-I) expression and upregulation of immune inhibitory molecules such as Programmed cell Death Ligand 1 (PD-L1).

Methods: The expression of PD-L1, HLA-I and CXCL10 was evaluated in the human β cell line, ECN90, and in primary human and mouse pancreatic islets. Most genes were determined by real-time RT-PCR, flow cytometry and Western blot. Activator and inhibitor of the AKT signaling were used to modulate PD-L1 induction. Key results were validated by monitoring activity of CD8+ Jurkat T cells presenting β cell specific T-cell receptor and transduced with reporter genes in contact culture with the human β cell line, ECN90.

Findings: In this study, we identify tryptophan (TRP) as an agonist of PD-L1 induction through the AKT signaling pathway. TRP also synergistically enhanced PD-L1 expression on β cells exposed to interferon-γ. Conversely, interferon-γ-mediated induction of HLA-I and CXCL10 genes was down-regulated upon TRP treatment. Finally, TRP and its derivatives inhibited the activation of islet-reactive CD8+ T cells by β cells.

Interpretation: Collectively, our findings indicate that TRP could induce immune tolerance to β cells by promoting their immune evasion through HLA-I downregulation and PD-L1 upregulation.

Funding: Dutch Diabetes Research Foundation, DON Foundation, the Laboratoire d'Excellence consortium Revive (ANR-10-LABX-0073), Agence Nationale de la Recherche (ANR-19-CE15-0014-01), Fondation pour la Recherche Médicale (EQ U201903007793-EQU20193007831), Innovative Medicines InitiativeINNODIA and INNODIA HARVEST, Aides aux Jeunes Diabetiques (AJD) and Juvenile Diabetes Research Foundation Ltd (JDRF).

Keywords: CD274; CXCL10; HLA-I; Immune checkpoint inhibitor; Islet; PD-L1; Pancreatic beta cells; Tryptophan; Type 1 diabetes.

MeSH terms

  • Animals
  • B7-H1 Antigen
  • Diabetes Mellitus, Type 1*
  • Humans
  • Immune Evasion
  • Insulin-Secreting Cells* / metabolism
  • Interferon-gamma / metabolism
  • Mice
  • Proto-Oncogene Proteins c-akt
  • Tryptophan

Substances

  • Tryptophan
  • Interferon-gamma
  • B7-H1 Antigen
  • Proto-Oncogene Proteins c-akt