机构地区:[1]Department of Endocrinology&Metabolism,Guangdong Provincial Key Laboratory of Diabetology,The Third Affliated Hospital of Sun Yat-sen University,Guangzhou 510630,China [2]Department of Clinical Immunology,The Third Affliated Hospital of Sun Yat-sen University,Guangzhou 510630,China [3]VIP Medical Service Center,The Third Affliated Hospital of Sun Yat-sen University,Guangzhou 510630,China [4]State Key Laboratory of Ophthalmology,Zhongshan Ophthalmic Center,Sun Yat-sen University,Guangzhou 510060,China [5]Department of Gastrointestinal Surgery,The Third Affliated Hospital of Sun Yat-sen University,Guangzhou 510630,China [6]Department of Rheumatology,The Sixth Affliated Hospital of Guangzhou Medical University,Qingyuan People's Hospital,Qingyuan 511518,China [7]Division of Pediatric Nephrology,Rady Children's Hospital,University of California,San Diego,CA 92093-0831,USA
出 处:《Cellular & Molecular Immunology》2022年第7期791-804,共14页中国免疫学杂志(英文版)
基 金:This study was funded by the National Key R&D Program of China(2017YFA0105803);the National Natural Science Foundation of China(32000621 and 81770826);the Key Area R&D Program of Guangdong Province(2019B020227003);the Science and Technology Plan Project of Guangzhou City(202102010338 and 202007040003);the 5010 Clinical Research Projects of Sun Yat-sen University(2015015);the Dengfeng Plan High-level Hospital Construction Opening Project of Foshan Fourth People’s Hospital(FSSYKF-2020009).
摘 要:Type 2 diabetes(T2D)is highly associated with obesity.However,the factors that drive the transition from excessive weight gain to glucose metabolism disruption are still uncertain and seem to revolve around systemic immune disorder.Mucosal-associated invariant T(MAIT)cells,which are innate-like T cells that recognize bacterial metabolites,have been reported to be altered in obese people and to lead to metabolic dysfunction during obesity.By studying the immunophenotypes of blood MAIT cells from a cross-sectional cohort of obese participants with/without T2D,we found an elevation in CD27^(-)negative(CD27−)MAIT cells producing a high level of IL-17 under T2D obese conditions,which could be positively correlated with impaired glucose metabolism in obese people.We further explored microbial translocation caused by gut barrier dysfunction in obese people as a triggering factor of MAIT cell abnormalities.Specifically,accumulation of the bacterial strain Bacteroides ovatus in the peripheral blood drove IL-17^(-)producing CD27−MAIT cell expansion and could be associated with T2D risk in obese individuals.Overall,these results suggest that an aberrant gut microbiota–immune axis in obese people may drive or exacerbate T2D.Importantly,CD27−MAIT cell subsets and Bacteroides ovatus could represent targets for novel interventional strategies.Our findings extend current knowledge regarding the clinical relevance of body mass index(BMI)-associated variation in circulating MAIT cells to reveal the role of these cells in obesity-related T2D progression and the underlying cellular mechanisms.
关 键 词:type 2 diabetes OBESITY MAIT cells Bacteroides ovatus bacterial translocation
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...