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肠道-口腔轴上的病原体反应性 Th17 细胞引发炎症性口腔疾病,并受肠道微生物组调节。

Pathobiont-responsive Th17 cells in gut-mouth axis provoke inflammatory oral disease and are modulated by intestinal microbiome.

机构信息

Section of Infection Biology, Department of Functional Bioscience, Fukuoka Dental College, Fukuoka 814-0193, Japan; Oral Medicine Research Center, Fukuoka Dental College, Fukuoka 814-0193, Japan.

Section of Infection Biology, Department of Functional Bioscience, Fukuoka Dental College, Fukuoka 814-0193, Japan.

出版信息

Cell Rep. 2022 Sep 6;40(10):111314. doi: 10.1016/j.celrep.2022.111314.

Abstract

Host immune response via Th17 cells against oral pathobionts is a key mediator in periodontitis development. However, where and how the Th17-type immune response is induced during the development of periodontitis is not well understood. Here, we demonstrate that gut translocation of the oral pathobiont Porphyromonas gingivalis (Pg) exacerbates oral pathobiont-induced periodontitis with enhanced Th17 cell differentiation. The oral pathobiont-responsive Th17 cells are differentiated in Peyer's patches and translocated systemically in the peripheral immune tissues. They are also capable of migrating to and accumulating in the mouth upon oral infection. Development of periodontitis via the oral pathobiont-responsive Th17 cells is regulated by the intestinal microbiome, and altering the intestinal microbiome composition with antibiotics affects the development of periodontitis. Our study highlights that pathobiont-responsive Th17 cells in the gut-mouth axis and the intestinal microbiome work together to provoke inflammatory oral diseases, including periodontitis.

摘要

宿主通过 Th17 细胞对口腔共生菌的免疫应答是牙周炎发展的关键介质。然而,在牙周炎发展过程中,Th17 型免疫应答是如何被诱导的还不是很清楚。在这里,我们证明了口腔共生菌牙龈卟啉单胞菌(Pg)的肠道易位会加剧口腔共生菌诱导的牙周炎,导致 Th17 细胞分化增强。口腔共生菌反应性 Th17 细胞在派尔集合淋巴结中分化,并在全身外周免疫组织中移位。它们也能够在口腔感染时迁移并积聚在口腔中。通过口腔共生菌反应性 Th17 细胞引发的牙周炎受肠道微生物组调控,而抗生素改变肠道微生物组组成会影响牙周炎的发展。我们的研究强调了肠道-口腔轴上的共生菌反应性 Th17 细胞和肠道微生物组共同作用,引发包括牙周炎在内的炎症性口腔疾病。

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