Journal
SCIENCE IMMUNOLOGY
Volume 2, Issue 10, Pages -Publisher
AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/sciimmunol.aai7616
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Funding
- Canadian Institutes of Health Research (CIHR) [119414, 132562, 142708, 148385]
- J.P. Bickell Foundation Grant
- Canada Research Chair
- Ontario Ministry of Innovation Early Researcher Award
- CIHR Canada Graduate Scholarship-Master's Program award
- Alfred Benzon Foundation Postdoctoral Fellowship
- CDA Postdoctoral Fellowship Award
- Canadian Diabetes Association (CDA) [OG-3-15-5014, CS-5-12-3886]
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Obesity-related insulin resistance is driven by low-grade chronic inflammation of metabolic tissues. In the liver, nonalcoholic fatty liver disease (NAFLD) is associated with hepatic insulin resistance and systemic glucose dysregulation. However, the immunological factors supporting these processes are poorly understood. We found that the liver accumulates pathogenic CD8(+) T cell subsets, which control hepatic insulin sensitivity and gluconeogenesis during diet-induced obesity in mice. In a cohort of human patients, CD8(+) T cells represent a dominant intrahepatic immune cell population that is linked to glucose dysregulation. Accumulation and activation of these cells are supported by type I interferon (IFN-I) responses in the liver. Livers from obese mice up-regulate critical interferon regulatory factors (IRF5), interferon stimulatory genes (ISGs), and IFN alpha protein, whereas IFN alpha R1(-/-) mice or CD8-specific IFN alpha R1(-/-) chimeric mice are protected from disease. IFN alpha R1 inhibitors improve metabolic parameters in mice, whereas CD8(+) T cells and IFN-I responses correlate with NAFLD in human patients. Thus, IFN-I responses represent a central immunological axis that governs intrahepatic T cell pathogenicity during metabolic disease.
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