Gut microbiota mediated T cells regulation and autoimmune diseases

Gut microbiota regulates the immune system, the development and progression of autoimmune diseases (AIDs) and overall health. Recent studies have played a crucial part in understanding the specific role of different gut bacterial strains and their metabolites in different AIDs. Microbial signatures...

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Main Authors: Nabeel Khalid Bhutta, Xiujin Xu, Cuiqin Jian, Yifan Wang, Yi Liu, Jinlyu Sun, Bingnan Han, Shandong Wu, Ansar Javeed
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-12-01
Series:Frontiers in Microbiology
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Online Access:https://www.frontiersin.org/articles/10.3389/fmicb.2024.1477187/full
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author Nabeel Khalid Bhutta
Xiujin Xu
Cuiqin Jian
Yifan Wang
Yi Liu
Jinlyu Sun
Bingnan Han
Shandong Wu
Ansar Javeed
author_facet Nabeel Khalid Bhutta
Xiujin Xu
Cuiqin Jian
Yifan Wang
Yi Liu
Jinlyu Sun
Bingnan Han
Shandong Wu
Ansar Javeed
author_sort Nabeel Khalid Bhutta
collection DOAJ
description Gut microbiota regulates the immune system, the development and progression of autoimmune diseases (AIDs) and overall health. Recent studies have played a crucial part in understanding the specific role of different gut bacterial strains and their metabolites in different AIDs. Microbial signatures in AIDs are revealed by advanced sequencing and metabolomics studies. Microbes such as Faecalibacterium prausnitzii, Akkermansia muciniphila, Anaerostipes caccae, Bacteroides sp., Roseburia sp., Blautia sp., Blautia faecis, Clostridium lavalense, Christensenellaceae sp., Coprococcus sp., Firmicutes sp., Ruminococcaceae sp., Lachnospiraceae sp., Megamonas sp., Monoglobus sp., Streptococcus pneumoniae and Bifidobacterium sp. help maintain immune homeostasis; whereas, Prevotella copri, Ruminococcus gnavus, Lactobacillus salivarius, Enterococcus gallinarum, Elizabeth menigoseptica, Collinsella sp., Escherichia sp., Fusobacterium sp., Enterobacter ludwigii, Enterobacteriaceae sp., Proteobacteria, Porphyromonas gingivalis, Porphyromonas nigrescens, Dorea sp., and Clostridium sp. cause immuno-pathogenesis. A complex web of interactions is revealed by understanding the influence of gut microbiota on immune cells and various T cell subsets such as CD4+ T cells, CD8+ T cells, natural killer T cells, γδ T cells, etc. Certain AIDs, including rheumatoid arthritis, diabetes mellitus, atopic asthma, inflammatory bowel disease and non-alcoholic fatty liver disease exhibit a state of dysbiosis, characterized by alterations in microbial diversity and relative abundance of specific taxa. This review summarizes recent developments in understanding the role of certain microbiota composition in specific AIDs, and the factors affecting specific regulatory T cells through certain microbial metabolites and also focuses the potential application and therapeutic significance of gut microbiota-based interventions as novel adjunctive therapies for AIDs. Further research to determine the precise association of each gut bacterial strain in specific diseases is required.
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spelling doaj-art-ffc759fdd74d43b99cab591f7bcd56b12024-12-19T16:37:51ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2024-12-011510.3389/fmicb.2024.14771871477187Gut microbiota mediated T cells regulation and autoimmune diseasesNabeel Khalid Bhutta0Xiujin Xu1Cuiqin Jian2Yifan Wang3Yi Liu4Jinlyu Sun5Bingnan Han6Shandong Wu7Ansar Javeed8Laboratory of Anti-allergic Functional Molecules, College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, ChinaLaboratory of Anti-allergic Functional Molecules, College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, ChinaLaboratory of Anti-allergic Functional Molecules, College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, ChinaLaboratory of Anti-allergic Functional Molecules, College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, ChinaHangzhou Zheda Dixun Biological Gene Engineering Co., Ltd., Hangzhou, ChinaBeijing Key Laboratory of Precision Medicine for Diagnosis and Treatment of Allergic Diseases, Department of Allergy, National Clinical Research Center for Dermatologic and Immunologic Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, ChinaLaboratory of Anti-allergic Functional Molecules, College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, ChinaHangzhou Zheda Dixun Biological Gene Engineering Co., Ltd., Hangzhou, ChinaLaboratory of Anti-allergic Functional Molecules, College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, ChinaGut microbiota regulates the immune system, the development and progression of autoimmune diseases (AIDs) and overall health. Recent studies have played a crucial part in understanding the specific role of different gut bacterial strains and their metabolites in different AIDs. Microbial signatures in AIDs are revealed by advanced sequencing and metabolomics studies. Microbes such as Faecalibacterium prausnitzii, Akkermansia muciniphila, Anaerostipes caccae, Bacteroides sp., Roseburia sp., Blautia sp., Blautia faecis, Clostridium lavalense, Christensenellaceae sp., Coprococcus sp., Firmicutes sp., Ruminococcaceae sp., Lachnospiraceae sp., Megamonas sp., Monoglobus sp., Streptococcus pneumoniae and Bifidobacterium sp. help maintain immune homeostasis; whereas, Prevotella copri, Ruminococcus gnavus, Lactobacillus salivarius, Enterococcus gallinarum, Elizabeth menigoseptica, Collinsella sp., Escherichia sp., Fusobacterium sp., Enterobacter ludwigii, Enterobacteriaceae sp., Proteobacteria, Porphyromonas gingivalis, Porphyromonas nigrescens, Dorea sp., and Clostridium sp. cause immuno-pathogenesis. A complex web of interactions is revealed by understanding the influence of gut microbiota on immune cells and various T cell subsets such as CD4+ T cells, CD8+ T cells, natural killer T cells, γδ T cells, etc. Certain AIDs, including rheumatoid arthritis, diabetes mellitus, atopic asthma, inflammatory bowel disease and non-alcoholic fatty liver disease exhibit a state of dysbiosis, characterized by alterations in microbial diversity and relative abundance of specific taxa. This review summarizes recent developments in understanding the role of certain microbiota composition in specific AIDs, and the factors affecting specific regulatory T cells through certain microbial metabolites and also focuses the potential application and therapeutic significance of gut microbiota-based interventions as novel adjunctive therapies for AIDs. Further research to determine the precise association of each gut bacterial strain in specific diseases is required.https://www.frontiersin.org/articles/10.3389/fmicb.2024.1477187/fullmuciniphilaAnaerostipes caccaeBacteroides sp.Roseburia sp.Blautia sp.Blautia faecis
spellingShingle Nabeel Khalid Bhutta
Xiujin Xu
Cuiqin Jian
Yifan Wang
Yi Liu
Jinlyu Sun
Bingnan Han
Shandong Wu
Ansar Javeed
Gut microbiota mediated T cells regulation and autoimmune diseases
Frontiers in Microbiology
muciniphila
Anaerostipes caccae
Bacteroides sp.
Roseburia sp.
Blautia sp.
Blautia faecis
title Gut microbiota mediated T cells regulation and autoimmune diseases
title_full Gut microbiota mediated T cells regulation and autoimmune diseases
title_fullStr Gut microbiota mediated T cells regulation and autoimmune diseases
title_full_unstemmed Gut microbiota mediated T cells regulation and autoimmune diseases
title_short Gut microbiota mediated T cells regulation and autoimmune diseases
title_sort gut microbiota mediated t cells regulation and autoimmune diseases
topic muciniphila
Anaerostipes caccae
Bacteroides sp.
Roseburia sp.
Blautia sp.
Blautia faecis
url https://www.frontiersin.org/articles/10.3389/fmicb.2024.1477187/full
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