科研成果详情

题名Partial Depletion of Regulatory T Cells Enhances Host Inflammatory Response Against Acute Pseudomonas aeruginosa Infection After Sepsis
作者
发表日期2018-10
发表期刊INFLAMMATION   影响因子和分区
语种英语
原始文献类型Article
关键词sepsis secondary infection nosocomial infection sepsis regulatory T cells CD25
其他关键词INTENSIVE-CARE UNITS ; IMMUNE DYSFUNCTION ; NOSOCOMIAL INFECTION ; SEPTIC SHOCK ; MICE ; LUNG ; IMMUNOSUPPRESSION ; PROTECTS
摘要Immune dysfunction contributes to secondary infection and worse outcomes in sepsis. Regulatory T cells (Tregs) have been implicated in sepsis-induced immunosuppression. Nevertheless, the role of Tregs in secondary infection after sepsis remains to be determined. In the present study, a two-hit model which mimics clinical conditions was used and the potential role of Tregs in secondary Pseudomonas aeruginosa infection post-sepsis was investigated. Results showed that mice were susceptible to secondary P. aeruginosa infection 3days, but not 7days, post-cecal ligation and puncture (CLP). The levels of IL-17A, IL-1, and IL-6 remained low in CLP mice after P. aeruginosa infection, while the levels of IL-10 increased significantly. Additionally, increased number of Tregs in both lung and spleen was observed in two-hit mice. Injection with PC61 (anti-CD25) mAb reduced the number of Tregs by 50% in spleen and 60% in lung of septic mice. This partial depletion of Tregs elevated IL-17A, IL-1, and IL-6 production and decreased IL-10 levels in septic mice with P. aeruginosa infection, leading to lower bacterial load, attenuation of lung injury, and improvement of survival. The present findings demonstrate that Tregs play a crucial role in secondary P. aeruginosa infection after sepsis by modulating the inflammatory response.
资助项目National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [81401621] Funding Source: Medline; Natural Science Foundation of Zhejiang ProvinceNatural Science Foundation of Zhejiang Province [LY13H150004] Funding Source: Medline; Wenzhou Municipal Science and Technology Project [2015KYB239] Funding Source: Medline; Excellent Young Talents Program of Traditional Chinese Medicine of Zhejiang Province [2013ZQ023] Funding Source: Medline
出版者SPRINGER/PLENUM PUBLISHERS
出版地NEW YORK
ISSN0360-3997
EISSN1573-2576
卷号41期号:5页码:1780-1790
DOI10.1007/s10753-018-0821-8
页数11
WOS类目Cell Biology ; Immunology
WOS研究方向Cell Biology ; Immunology
WOS记录号WOS:000444287600021
收录类别SCIE ; PUBMED ; SCOPUS
URL查看原文
PubMed ID29956070
SCOPUSEID2-s2.0-85049146087
通讯作者地址[Lu, Zhong-qiu]Emergency Department,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,325000,China
Scopus学科分类Immunology and Allergy;Immunology
引用统计
被引频次:11[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符https://kms.wmu.edu.cn/handle/3ETUA0LF/4816
专题附属第一医院
护理学院
通讯作者Lu, Zhong-qiu
作者单位
1.Emergency Department,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,325000,China;
2.Wenzhou Key Laboratory of Emergency,Critical Care,and Disaster Medicine,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,325000,China;
3.College of Nursing,Wenzhou Medical University,Wenzhou,325000,China;
4.Burns Institute,First Affiliated Hospital of PLA General Hospital,Beijing,100048,China;
5.Intensive Care Unit,Ningbo First Hospital,Ningbo,315000,China
第一作者单位附属第一医院;  第一临床医学院(信息与工程学院)、附属第一医院
通讯作者单位附属第一医院;  第一临床医学院(信息与工程学院)、附属第一医院
第一作者的第一单位附属第一医院
推荐引用方式
GB/T 7714
Hu, Zhi-qiang,Yao, Yong-ming,Chen, Wei,et al. Partial Depletion of Regulatory T Cells Enhances Host Inflammatory Response Against Acute Pseudomonas aeruginosa Infection After Sepsis[J]. INFLAMMATION,2018,41(5):1780-1790.
APA Hu, Zhi-qiang., Yao, Yong-ming., Chen, Wei., Bian, Jia-lan., Zhao, Lin-jun., ... & Zhao, Guang-ju. (2018). Partial Depletion of Regulatory T Cells Enhances Host Inflammatory Response Against Acute Pseudomonas aeruginosa Infection After Sepsis. INFLAMMATION, 41(5), 1780-1790.
MLA Hu, Zhi-qiang,et al."Partial Depletion of Regulatory T Cells Enhances Host Inflammatory Response Against Acute Pseudomonas aeruginosa Infection After Sepsis".INFLAMMATION 41.5(2018):1780-1790.

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