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炎症性肠病。

Inflammatory bowel disease.

机构信息

Department of Medicine II, Medical University Innsbruck, Austria.

出版信息

Annu Rev Immunol. 2010;28:573-621. doi: 10.1146/annurev-immunol-030409-101225.


DOI:10.1146/annurev-immunol-030409-101225
PMID:20192811
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4620040/
Abstract

Insights into inflammatory bowel disease (IBD) are advancing rapidly owing to immunologic investigations of a plethora of animal models of intestinal inflammation, ground-breaking advances in the interrogation of diseases that are inherited as complex genetic traits, and the development of culture-independent methods to define the composition of the intestinal microbiota. These advances are bringing a deeper understanding to the genetically determined interplay between the commensal microbiota, intestinal epithelial cells, and the immune system and the manner in which this interplay might be modified by relevant environmental factors in the pathogenesis of IBD. This review examines these interactions and, where possible, potential lessons from IBD-directed, biologic therapies that may allow for elucidation of pathways that are central to disease pathogenesis in humans.

摘要

由于对大量肠道炎症动物模型的免疫学研究、对作为复杂遗传特征遗传疾病的突破性研究,以及对定义肠道微生物组组成的非培养方法的发展,人们对炎症性肠病(IBD)的认识正在迅速深入。这些进展使人们对共生微生物群、肠上皮细胞和免疫系统之间由遗传决定的相互作用,以及这种相互作用如何被 IBD 发病机制中的相关环境因素改变有了更深入的了解。这篇综述检查了这些相互作用,并在可能的情况下,从针对 IBD 的生物治疗中吸取了一些教训,这些治疗可能有助于阐明对人类疾病发病机制至关重要的途径。

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本文引用的文献

[1]
NOD2 stimulation induces autophagy in dendritic cells influencing bacterial handling and antigen presentation.

Nat Med. 2009-12-6

[2]
Nod1 and Nod2 direct autophagy by recruiting ATG16L1 to the plasma membrane at the site of bacterial entry.

Nat Immunol. 2009-11-8

[3]
Inflammatory bowel disease and mutations affecting the interleukin-10 receptor.

N Engl J Med. 2009-11-19

[4]
A dominant, coordinated T regulatory cell-IgA response to the intestinal microbiota.

Proc Natl Acad Sci U S A. 2009-11-17

[5]
T cell-intrinsic role of Nod2 in promoting type 1 immunity to Toxoplasma gondii.

Nat Immunol. 2009-12

[6]
Regulation of inflammatory responses by gut microbiota and chemoattractant receptor GPR43.

Nature. 2009-10-29

[7]
Endoplasmic reticulum stress and intestinal inflammation.

Mucosal Immunol. 2009-10-28

[8]
Induction of intestinal Th17 cells by segmented filamentous bacteria.

Cell. 2009-10-30

[9]
The key role of segmented filamentous bacteria in the coordinated maturation of gut helper T cell responses.

Immunity. 2009-10-16

[10]
Nod2 is required for the regulation of commensal microbiota in the intestine.

Proc Natl Acad Sci U S A. 2009-9-15

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