Gut microbiota in Celiac Disease: microbes, metabolites, pathways and therapeutics

被引:22
|
作者
Olshan, Katherine L. [1 ,2 ,3 ]
Leonard, Maureen M. [1 ,2 ,3 ]
Serena, Gloria [1 ,2 ,3 ]
Zomorrodi, Ali R. [1 ,2 ,3 ]
Fasano, Alessio [1 ,2 ,4 ]
机构
[1] Harvard Med Sch, MassGen Hosp Children, Div Pediat Gastroenterol & Nutr, Boston, MA 02115 USA
[2] Harvard Med Sch, MassGen Hosp Children, Mucosal Immunol & Biol Res Ctr, Boston, MA 02115 USA
[3] Harvard Med Sch, Celiac Res Program, Boston, MA 02115 USA
[4] European Biomed Res Inst Salerno EBRIS, Salerno, Italy
关键词
Celiac disease; dysbiosis; gluten; gut; microbiome; microbiota; INTESTINAL MICROBIOTA; BARRIER FUNCTION; EARLY-LIFE; ESCHERICHIA-COLI; T-CELLS; BACTERIAL COMMUNITIES; BACTEROIDES-VULGATUS; DUODENAL MICROBIOTA; HEALTHY-VOLUNTEERS; GLUTEN METABOLISM;
D O I
10.1080/1744666X.2021.1840354
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction Current evidence supports a vital role of the microbiota on health outcomes, with alterations in an otherwise healthy balance linked to chronic medical conditions like celiac disease (CD). Recent advances in microbiome analysis allow for unparalleled profiling of the microbes and metabolites. With the growing volume of data available, trends are emerging that support a role for the gut microbiota in CD pathogenesis. Areas covered In this article, the authors review the relationship between factors such as genes and antibiotic exposure on CD onset and the intestinal microbiota. The authors also review other microbiota within the human body (like the oropharynx) that may play a role in CD pathogenesis. Finally, the authors discuss implications for disease modification and the ultimate goal of prevention. The authors reviewed literature from PubMed, EMBASE, and Web of Science. Expert opinion CD serves as a unique opportunity to explore the role of the intestinal microbiota on the development of chronic autoimmune disease. While research to date provides a solid foundation, most studies have been case-control and thus do not have capacity to explore the mechanistic role of the microbiota in CD onset. Further longitudinal studies and integrated multi-omics are necessary for investigating CD pathogenesis.
引用
收藏
页码:1075 / 1092
页数:18
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