Loss of gut barrier integrity triggers activation of islet-reactive T cells and autoimmune diabetes

被引:173
作者
Sorini, Chiara [1 ,2 ]
Cosorich, Ilaria [1 ]
Lo Conte, Marta [1 ]
De Giorgi, Lorena [1 ]
Facciotti, Federica [3 ]
Luciano, Roberta [4 ]
Rocchi, Martina [4 ]
Ferrarese, Roberto [1 ]
Sanvito, Francesca [4 ]
Canducci, Filippo [5 ]
Falcone, Marika [1 ]
机构
[1] IRCCS San Raffaele Sci Inst, Div Immunol Transplantat & Infect Dis, Expt Diabet Unit, I-20132 Milan, Italy
[2] Karolinska Inst, Dept Med, Immunol & Allergy Unit, SE-17177 Stockholm, Sweden
[3] European Inst Oncol IRCSS, Dept Expt Oncol, I-20139 Milan, Italy
[4] IRCSS San Raffaele Sci Inst, Pathol Anat Unit, I-20132 Milan, Italy
[5] Univ Insubria, Dept Biotechnol & Life Sci, I-21100 Varese, Italy
关键词
autoimmune diabetes; microbiota; gut inflammation; INCREASED INTESTINAL PERMEABILITY; CHROMOGRANIN-A; GASTROENTEROPANCREATIC SYSTEM; LYMPH-NODES; BETA-CELLS; TYPE-1; MICROBIOTA; MUCUS; ONSET; MICE;
D O I
10.1073/pnas.1814558116
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Low-grade intestinal inflammation and alterations of gut barrier integrity are found in patients affected by extraintestinal autoimmune diseases such as type 1 diabetes (T1D), but a direct causal link between enteropathy and triggering of autoimmunity is yet to be established. Here, we found that onset of autoimmunity in preclinical models of T1D is associated with alterations of the mucus layer structure and loss of gut barrier integrity. Importantly, we showed that breakage of the gut barrier integrity in BDC2.5XNOD mice carrying a transgenic T cell receptor (TCR) specific for a beta cell auto-antigen leads to activation of islet-reactive T cells within the gut mucosa and onset of T1D. The intestinal activation of islet-reactive T cells requires the presence of gut microbiota and is abolished when mice are depleted of endogenous commensal microbiota by antibiotic treatment. Our results indicate that loss of gut barrier continuity can lead to activation of islet-specific T cells within the intestinal mucosa and to autoimmune diabetes and provide a strong rationale to design innovative therapeutic interventions in "at-risk" individuals aimed at restoring gut barrier integrity to prevent T1D occurrence.
引用
收藏
页码:15140 / 15149
页数:10
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