CXCL16-dependent scavenging of oxidized lipids by islet macrophages promotes differentiation of pathogenic CD8+ T cells in diabetic autoimmunity

Immunity. 2024 Jul 9;57(7):1629-1647.e8. doi: 10.1016/j.immuni.2024.04.017. Epub 2024 May 15.

Abstract

The pancreatic islet microenvironment is highly oxidative, rendering β cells vulnerable to autoinflammatory insults. Here, we examined the role of islet resident macrophages in the autoimmune attack that initiates type 1 diabetes. Islet macrophages highly expressed CXCL16, a chemokine and scavenger receptor for oxidized low-density lipoproteins (OxLDLs), regardless of autoimmune predisposition. Deletion of Cxcl16 in nonobese diabetic (NOD) mice suppressed the development of autoimmune diabetes. Mechanistically, Cxcl16 deficiency impaired clearance of OxLDL by islet macrophages, leading to OxLDL accumulation in pancreatic islets and a substantial reduction in intra-islet transitory (Texint) CD8+ T cells displaying proliferative and effector signatures. Texint cells were vulnerable to oxidative stress and diminished by ferroptosis; PD-1 blockade rescued this population and reversed diabetes resistance in NOD.Cxcl16-/- mice. Thus, OxLDL scavenging in pancreatic islets inadvertently promotes differentiation of pathogenic CD8+ T cells, presenting a paradigm wherein tissue homeostasis processes can facilitate autoimmune pathogenesis in predisposed individuals.

Keywords: CD8 T cell differentiation; CD8 T cell exhaustion; CD8 T cell ferroptosis; CXCL16; PD-1 checkpoint blockade; autoimmunity; oxidized LDL; pancreatic islets; tissue-resident macrophages; type 1 diabetes.

MeSH terms

  • Animals
  • Autoimmunity*
  • CD8-Positive T-Lymphocytes* / immunology
  • CD8-Positive T-Lymphocytes* / metabolism
  • Cell Differentiation*
  • Chemokine CXCL16* / metabolism
  • Diabetes Mellitus, Type 1* / immunology
  • Diabetes Mellitus, Type 1* / metabolism
  • Islets of Langerhans* / immunology
  • Islets of Langerhans* / metabolism
  • Lipoproteins, LDL* / immunology
  • Lipoproteins, LDL* / metabolism
  • Macrophages* / immunology
  • Macrophages* / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred NOD*
  • Mice, Knockout*

Substances

  • Lipoproteins, LDL
  • oxidized low density lipoprotein
  • Chemokine CXCL16
  • Cxcl16 protein, mouse