2018
DOI: 10.1080/19490976.2018.1448742
|View full text |Cite
|
Sign up to set email alerts
|

The role of inflammation in temporal shifts in the inflammatory bowel disease mucosal microbiome

Abstract: Studies of the human intestinal microbiome in patients with inflammatory bowel disease (IBD) consistently show that there are differences (an abnormal or unbalanced microbiome, “dysbiosis”) when compared to healthy subjects. We sought to describe changes in the microbiome in individual patients over time, and determine the clinical factors that are associated with significant alteration. Forty-two mucosal biopsies were collected from 20 patients that were spaced an average of 2.4 years apart. These were analys… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
31
0

Year Published

2019
2019
2020
2020

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 37 publications
(31 citation statements)
references
References 44 publications
(38 reference statements)
0
31
0
Order By: Relevance
“…Another study reveals that RegIIIb‐target recognition, killing of Gram‐negative bacteria in infectious diarrhea, proposes avenues toward novel therapeutic interventions for Salmonella diarrhea (Miki, Okada, & Hardt, ). Using human patient specimens, Kiely, Pavli, and O'Brien () demonstrated that inflammation is related to microbiome, which is spatially and timely altered in inflammatory bowel disease (IBD). Interestingly, Mamantopoulos, Ronchi, McCoy, and Wullaert () analyzed the association between maternal inheritance and long‐term separate housing and host–microbiota interactions, illustrating the importance of host–microbiota and inflammatory responses.…”
Section: Discussionmentioning
confidence: 99%
“…Another study reveals that RegIIIb‐target recognition, killing of Gram‐negative bacteria in infectious diarrhea, proposes avenues toward novel therapeutic interventions for Salmonella diarrhea (Miki, Okada, & Hardt, ). Using human patient specimens, Kiely, Pavli, and O'Brien () demonstrated that inflammation is related to microbiome, which is spatially and timely altered in inflammatory bowel disease (IBD). Interestingly, Mamantopoulos, Ronchi, McCoy, and Wullaert () analyzed the association between maternal inheritance and long‐term separate housing and host–microbiota interactions, illustrating the importance of host–microbiota and inflammatory responses.…”
Section: Discussionmentioning
confidence: 99%
“…In a study conducted in 2008, F. prausnitzii was reported to protect from inflammation in vitro and in vivo through blocking NF-κB activation and IL8 production [21]. Meanwhile, both F. prausnitzii and its culture supernatant could exhibit anti-inflammatory effects under recovery from chronic colitis and colitis reactivation [22][23][24]. Umesaki and his colleagues found that a defined mixture of 46 strains of Clostridium species belonging to Clostridium clusters XIVa and IV could modify the intraepithelial lymphocytes profile in large intestine [19].…”
Section: Benefits From Crosstalk Between Clostridium Species and Intementioning
confidence: 99%
“…Oxidative pressure can be generated by the external environment and internal resources, causing some of the primary damage resulting from the peroxide (e.g., ROS, superoxide radical, hydroxyl radical and hydrogen peroxide) . The lack of antioxidants leads to oxidative stress and excessive free radicals, which affect the structure of the protein and making the function abnormal.…”
Section: Discussionmentioning
confidence: 99%
“…Oxidative pressure can be generated by the external environment and internal resources, causing some of the primary damage resulting from the peroxide (e.g., ROS, superoxide radical, hydroxyl radical and hydrogen peroxide). [37][38][39][40][41][42][43][44] The lack of antioxidants leads to oxidative stress and excessive free radicals, which affect the structure of the protein and making the function abnormal. Reactive oxygen species attack and react with stable skin cell molecules, causing cross-linking of collagen and elastin and reducing the skin's ability to repair itself.…”
Section: Hscae Reduced the Ros Produced By Uvb In Hs68 Cellsmentioning
confidence: 99%