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长五聚素 PTX3 对炎症的调节作用和对侵袭性肺炎球菌感染的保护作用。

Regulation of inflammation and protection against invasive pneumococcal infection by the long pentraxin PTX3.

机构信息

IRCCS Humanitas Research Hospital, Milan, Italy.

Department of Biomedical Sciences, Humanitas University, Milan, Italy.

出版信息

Elife. 2023 May 24;12:e78601. doi: 10.7554/eLife.78601.

Abstract

is a major pathogen in children, elderly subjects, and immunodeficient patients. Pentraxin 3 (PTX3) is a fluid-phase pattern recognition molecule (PRM) involved in resistance to selected microbial agents and in regulation of inflammation. The present study was designed to assess the role of PTX3 in invasive pneumococcal infection. In a murine model of invasive pneumococcal infection, PTX3 was strongly induced in non-hematopoietic (particularly, endothelial) cells. The IL-1β/MyD88 axis played a major role in regulation of the gene expression. mice presented more severe invasive pneumococcal infection. Although high concentrations of PTX3 had opsonic activity in vitro, no evidence of PTX3-enhanced phagocytosis was obtained in vivo. In contrast, -deficient mice showed enhanced recruitment of neutrophils and inflammation. Using deficient mice, we found that protection against pneumococcus was dependent upon PTX3-mediated regulation of neutrophil inflammation. In humans, gene polymorphisms were associated with invasive pneumococcal infections. Thus, this fluid-phase PRM plays an important role in tuning inflammation and resistance against invasive pneumococcal infection.

摘要

是儿童、老年患者和免疫功能低下患者的主要病原体。五聚素 3(PTX3)是一种参与抵抗某些微生物和调节炎症的体液模式识别分子(PRM)。本研究旨在评估 PTX3 在侵袭性肺炎球菌感染中的作用。在侵袭性肺炎球菌感染的小鼠模型中,PTX3 在非造血细胞(特别是内皮细胞)中被强烈诱导。IL-1β/MyD88 轴在调节 基因表达中起主要作用。PTX3 缺陷小鼠表现出更严重的侵袭性肺炎球菌感染。尽管 PTX3 在体外具有调理活性,但在体内未获得 PTX3 增强吞噬作用的证据。相反,PTX3 缺陷小鼠显示中性粒细胞募集和炎症增强。使用缺陷小鼠,我们发现对肺炎球菌的保护作用取决于 PTX3 介导的中性粒细胞炎症调节。在人类中,基因多态性与侵袭性肺炎球菌感染有关。因此,这种体液 PRM 在调节炎症和抵抗侵袭性肺炎球菌感染方面发挥着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d64/10266767/fbc97aa3f12d/elife-78601-fig1.jpg

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