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住院的百日咳博德特氏菌、鼻病毒或合并感染患儿的细胞因子表达模式。

Cytokine expression patterns in hospitalized children with Bordetella pertussis, Rhinovirus or co-infection.

机构信息

Multifactorial Disease and Complex Phenotype Research Area, Bambino Gesù Children's Hospital (IRCCS), Piazza S. Onofrio, 4, 00165, Rome, Italy.

Research Unit of Molecular Genetics of Complex Phenotypes, Bambino Gesù Children's Hospital (IRCCS), Rome, Italy.

出版信息

Sci Rep. 2021 May 26;11(1):10948. doi: 10.1038/s41598-021-89538-0.

Abstract

Mechanisms of interaction between Bordetella pertussis and other viral agents are yet to be fully explored. We studied the inflammatory cytokine expression patterns among children with both viral-bacterial infections. Nasopharyngeal aspirate (NPA) samples were taken from children, aged < 1 year, positive for Rhinovirus, Bordetella pertussis and for Rhinovirus and Bordetella pertussis. Forty cytokines were evaluated in NPA by using human cytokine protein arrays and a quantitative analysis was performed on significantly altered cytokines. Forty cytokines were evaluated in NPA by using human cytokine protein arrays and a quantitative analysis was performed on significantly altered cytokines. Our results show that co-infections display a different inflammatory pattern compared to single infections, suggesting that a chronic inflammation caused by one of the two pathogens could be the trigger for exacerbation in co-infections.

摘要

百日咳博德特氏菌与其他病毒因子相互作用的机制尚未被充分研究。我们研究了同时患有病毒-细菌感染的儿童的炎症细胞因子表达模式。从年龄<1 岁、鼻病毒、百日咳博德特氏菌阳性和鼻病毒及百日咳博德特氏菌阳性的儿童中采集鼻咽抽吸物(NPA)样本。使用人细胞因子蛋白芯片评估 NPA 中的 40 种细胞因子,并对明显改变的细胞因子进行定量分析。使用人细胞因子蛋白芯片评估 NPA 中的 40 种细胞因子,并对明显改变的细胞因子进行定量分析。我们的研究结果表明,与单重感染相比,合并感染显示出不同的炎症模式,这表明两种病原体之一引起的慢性炎症可能是合并感染恶化的触发因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9e/8154898/8675f50a8e7c/41598_2021_89538_Fig1_HTML.jpg

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