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IBD immunopathogenesis: A comprehensive review of inflammatory molecules.

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TLDR
The roles of numerous inflammatory molecules including but not limited to cytokines, chemokines, inflammasomes, microRNAs and neuropeptides and their expression status in ulcerative colitis and Crohn's disease are discussed in relation to their effects on the overall intestinal inflammatory process.
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This article is published in Autoimmunity Reviews.The article was published on 2017-04-01. It has received 207 citations till now. The article focuses on the topics: Inflammatory bowel disease & Ulcerative colitis.

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Pea Albumin Attenuates Dextran Sulfate Sodium-Induced Colitis by Regulating NF-κB Signaling and the Intestinal Microbiota in Mice

TL;DR: In this paper , pea albumin from pea seeds was used to prevent colitis in dextran sulfate sodium (DSS)-challenged mice by reducing inflammatory cell infiltration, pro-inflammatory genes expression and cytokines release.
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Ag-NP-induced interleukin-1beta upregulation in a lung co-culture model

TL;DR: It is demonstrated here that interleukin-1beta is upregulated, both the transcript and the mature protein, following 24 hour exposure to 10 nm silver, but that caspase-1 function is downregulated, which prevents confirmation of the inflammasome activity.
References
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Journal ArticleDOI

Obesity is associated with macrophage accumulation in adipose tissue

TL;DR: Transcript expression in perigonadal adipose tissue from groups of mice in which adiposity varied due to sex, diet, and the obesity-related mutations agouti (Ay) and obese (Lepob) found that the expression of 1,304 transcripts correlated significantly with body mass.
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Molecular-phylogenetic characterization of microbial community imbalances in human inflammatory bowel diseases

TL;DR: Patient stratification by GI microbiota provides further evidence that CD represents a spectrum of disease states and suggests that treatment of some forms of IBD may be facilitated by redress of the detected microbiological imbalances.
Journal ArticleDOI

A novel transcription factor, T-bet, directs Th1 lineage commitment.

TL;DR: T-bet initiates Th1 lineage development from naive Thp cells both by activating Th1 genetic programs and by repressing the opposing Th2 programs, as evidenced by the simultaneous induction of IFNgamma and repression of IL-4 and IL-5.
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