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宿主对肠内阿米巴病的保护机制。

Host Protective Mechanisms to Intestinal Amebiasis.

机构信息

Division of Infectious Diseases and International Health, Department of Medicine, University of Virginia, Charlottesville, VA, USA.

Division of Infectious Diseases and International Health, Department of Medicine, University of Virginia, Charlottesville, VA, USA.

出版信息

Trends Parasitol. 2021 Feb;37(2):165-175. doi: 10.1016/j.pt.2020.09.015. Epub 2020 Oct 23.


DOI:10.1016/j.pt.2020.09.015
PMID:33502317
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7840892/
Abstract

The protozoan parasite Entamoeba histolytica is the causative agent of amebiasis, an infection that manifests as colitis and, in some cases, liver abscess. A better understanding of host protective factors is key to developing an effective remedy. Recently, significant advances have been made in understanding the mechanisms of MUC2 production by goblet cells upon amebic infection, regulation of antimicrobial peptide production by Paneth cells, the interaction of commensal microbiota with immune stimulation, and host genetics in conferring protection from amebiasis. In addition to host pathways that may serve as potential therapeutic targets, significant progress has also been made with respect to development of a vaccine against amebiasis. Here, we aim to highlight the current understanding and knowledge gaps critically.

摘要

原虫寄生虫溶组织内阿米巴原虫是阿米巴病的病原体,感染表现为结肠炎,在某些情况下还会导致肝脓肿。更好地了解宿主保护因素是开发有效治疗方法的关键。最近,人们在理解阿米巴感染时杯状细胞产生 MUC2 的机制、潘氏细胞产生抗菌肽的调节、共生微生物群与免疫刺激的相互作用以及宿主遗传学在赋予对阿米巴病的保护方面取得了重大进展。除了可能作为潜在治疗靶点的宿主途径外,在开发针对阿米巴病的疫苗方面也取得了重大进展。在这里,我们旨在批判性地强调当前的理解和知识差距。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f17/7840892/15e51ff96e06/nihms-1642829-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f17/7840892/e5bcc7f649e6/nihms-1642829-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f17/7840892/15e51ff96e06/nihms-1642829-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f17/7840892/e5bcc7f649e6/nihms-1642829-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f17/7840892/15e51ff96e06/nihms-1642829-f0002.jpg

相似文献

[1]
Host Protective Mechanisms to Intestinal Amebiasis.

Trends Parasitol. 2021-2

[2]
Host-pathogen interaction in amebiasis and progress in vaccine development.

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[3]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Muc2 Mucin and Nonmucin Microbiota Confer Distinct Innate Host Defense in Disease Susceptibility and Colonic Injury.

Cell Mol Gastroenterol Hepatol. 2021

[2]
Androgens predispose males to monocyte-mediated immunopathology by inducing the expression of leukocyte recruitment factor CXCL1.

Nat Commun. 2020-7-10

[3]
Gut microbiome communication with bone marrow regulates susceptibility to amebiasis.

J Clin Invest. 2020-8-3

[4]
CD74 Signaling Links Inflammation to Intestinal Epithelial Cell Regeneration and Promotes Mucosal Healing.

Cell Mol Gastroenterol Hepatol. 2020

[5]
Inhibition of Amebic Cysteine Proteases Blocks Amebic Trogocytosis but Not Phagocytosis.

J Infect Dis. 2020-4-27

[6]
Entamoeba histolytica stimulates the alarmin molecule HMGB1 from macrophages to amplify innate host defenses.

Mucosal Immunol. 2020-3

[7]
EhP3, a homolog of 14-3-3 family of protein participates in actin reorganization and phagocytosis in Entamoeba histolytica.

PLoS Pathog. 2019-5-16

[8]
Deficiency in intestinal epithelial Reg4 ameliorates intestinal inflammation and alters the colonic bacterial composition.

Mucosal Immunol. 2019-4-5

[9]
Neutrophils: New insights and open questions.

Sci Immunol. 2018-12-7

[10]
Defining cooperative roles for colonic microbiota and Muc2 mucin in mediating innate host defense against Entamoeba histolytica.

PLoS Pathog. 2018-11-30

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