Mucosal-associated invariant T cells promote inflammation and intestinal dysbiosis leading to metabolic dysfunction during obesity

Amine Toubal(Centre National de la Recherche Scientifique), Badr Kiaf(Centre National de la Recherche Scientifique), Lucie Beaudoin(Centre National de la Recherche Scientifique), Lucie Cagninacci(Centre National de la Recherche Scientifique), Moez Rhimi(Microbiologie de l’alimentation au service de la santé), Blandine Fruchet(Centre National de la Recherche Scientifique), Jennifer Da Silva(Centre National de la Recherche Scientifique), Alexandra J. Corbett(The University of Melbourne), Yannick Simoni(Centre National de la Recherche Scientifique), Olivier Lantz(Inserm), Jamie Rossjohn(Australian Regenerative Medicine Institute), James McCluskey(The University of Melbourne), Philippe Lesnik(Inserm), Emmanuelle Maguin(Microbiologie de l’alimentation au service de la santé), Agnès Lehuen(Centre National de la Recherche Scientifique)
Nature Communications
July 24, 2020
Cited by 156Open Access
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Abstract

Obesity is associated with low-grade chronic inflammation promoting insulin-resistance and diabetes. Gut microbiota dysbiosis is a consequence as well as a driver of obesity and diabetes. Mucosal-associated invariant T cells (MAIT) are innate-like T cells expressing a semi-invariant T cell receptor restricted to the non-classical MHC class I molecule MR1 presenting bacterial ligands. Here we show that during obesity MAIT cells promote inflammation in both adipose tissue and ileum, leading to insulin resistance and impaired glucose and lipid metabolism. MAIT cells act in adipose tissue by inducing M1 macrophage polarization in an MR1-dependent manner and in the gut by inducing microbiota dysbiosis and loss of gut integrity. Both MAIT cell-induced tissue alterations contribute to metabolic dysfunction. Treatment with MAIT cell inhibitory ligand demonstrates its potential as a strategy against inflammation, dysbiosis and metabolic disorders.


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