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本文引用的文献

1
Ibuprofen therapy resulted in significantly decreased tissue bacillary loads and increased survival in a new murine experimental model of active tuberculosis.布洛芬治疗可显著降低新的活动性结核小鼠实验模型中的组织细菌负荷并提高生存率。
J Infect Dis. 2013 Jul 15;208(2):199-202. doi: 10.1093/infdis/jit152. Epub 2013 Apr 5.
2
Tuberculosis.肺结核
N Engl J Med. 2013 Feb 21;368(8):745-55. doi: 10.1056/NEJMra1200894.
3
IL-10 inhibits mature fibrotic granuloma formation during Mycobacterium tuberculosis infection.白细胞介素-10 抑制结核分枝杆菌感染期间成熟的纤维性肉芽肿形成。
J Immunol. 2013 Mar 15;190(6):2778-90. doi: 10.4049/jimmunol.1202722. Epub 2013 Feb 8.
4
Inflammation, chronic obstructive pulmonary disease and aging.炎症、慢性阻塞性肺疾病与衰老。
Curr Opin Pulm Med. 2011 Dec;17 Suppl 1:S3-10. doi: 10.1097/01.mcp.0000410742.90463.1f.
5
Aging, inflammation, and emphysema.衰老、炎症与肺气肿。
Am J Respir Crit Care Med. 2011 Dec 15;184(12):1327-9. doi: 10.1164/rccm.201110-1764ED.
6
Prostaglandins and inflammation.前列腺素与炎症。
Arterioscler Thromb Vasc Biol. 2011 May;31(5):986-1000. doi: 10.1161/ATVBAHA.110.207449.
7
Aging of the innate immune system.固有免疫系统的衰老。
Curr Opin Immunol. 2010 Aug;22(4):507-13. doi: 10.1016/j.coi.2010.05.003.
8
TLR-2 independent recognition of Mycobacterium tuberculosis by CD11c+ pulmonary cells from old mice.老年小鼠肺部 CD11c+ 细胞对结核分枝杆菌的 TLR-2 非依赖性识别。
Mech Ageing Dev. 2010 Jun;131(6):405-14. doi: 10.1016/j.mad.2010.05.006. Epub 2010 Jun 8.
9
Mycobacterium tuberculosis activates human macrophage peroxisome proliferator-activated receptor gamma linking mannose receptor recognition to regulation of immune responses.结核分枝杆菌激活人巨噬细胞过氧化物酶体增殖物激活受体 γ,将甘露糖受体识别与免疫反应调节联系起来。
J Immunol. 2010 Jul 15;185(2):929-42. doi: 10.4049/jimmunol.1000866. Epub 2010 Jun 16.
10
Aging promotes neutrophil-induced mortality by augmenting IL-17 production during viral infection.衰老通过在病毒感染期间增强 IL-17 的产生促进中性粒细胞诱导的死亡。
Cell Host Microbe. 2009 Nov 19;6(5):446-56. doi: 10.1016/j.chom.2009.09.011.

衰老过程中肺部炎症的特征及其对巨噬细胞功能的影响。

Characterization of lung inflammation and its impact on macrophage function in aging.

作者信息

Canan Cynthia H, Gokhale Nandan S, Carruthers Bridget, Lafuse William P, Schlesinger Larry S, Torrelles Jordi B, Turner Joanne

机构信息

Department of Microbial Infection and Immunity, College of Medicine, and Center for Microbial Interface Biology, The Ohio State University, Columbus Ohio, USA.

Department of Microbial Infection and Immunity, College of Medicine, and Center for Microbial Interface Biology, The Ohio State University, Columbus Ohio, USA

出版信息

J Leukoc Biol. 2014 Sep;96(3):473-80. doi: 10.1189/jlb.4A0214-093RR. Epub 2014 Jun 16.

DOI:10.1189/jlb.4A0214-093RR
PMID:24935957
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4632167/
Abstract

Systemic inflammation that occurs with increasing age (inflammaging) is thought to contribute to the increased susceptibility of the elderly to several disease states. The elderly are at significant risk for developing pulmonary disorders and infectious diseases, but the contribution of inflammation in the pulmonary environment has received little attention. In this study, we demonstrate that the lungs of old mice have elevated levels of proinflammatory cytokines and a resident population of highly activated pulmonary macrophages that are refractory to further activation by IFN-γ. The impact of this inflammatory state on macrophage function was determined in vitro in response to infection with M.tb. Macrophages from the lungs of old mice secreted more proinflammatory cytokines in response to M.tb infection than similar cells from young mice and also demonstrated enhanced M.tb uptake and P-L fusion. Supplementation of mouse chow with the NSAID ibuprofen led to a reversal of lung and macrophage inflammatory signatures. These data indicate that the pulmonary environment becomes inflammatory with increasing age and that this inflammatory environment can be reversed with ibuprofen.

摘要

随着年龄增长而出现的全身炎症(炎症衰老)被认为是导致老年人对多种疾病易感性增加的原因。老年人患肺部疾病和传染病的风险很大,但炎症在肺部环境中的作用却很少受到关注。在本研究中,我们证明老年小鼠的肺部促炎细胞因子水平升高,并且存在一群高度活化的肺巨噬细胞,这些巨噬细胞对IFN-γ的进一步激活具有抗性。这种炎症状态对巨噬细胞功能的影响在体外通过结核分枝杆菌感染来确定。来自老年小鼠肺部的巨噬细胞在受到结核分枝杆菌感染时比来自年轻小鼠的类似细胞分泌更多的促炎细胞因子,并且还表现出增强的结核分枝杆菌摄取和吞噬体-溶酶体融合。在小鼠食物中添加非甾体抗炎药布洛芬可导致肺部和巨噬细胞炎症特征的逆转。这些数据表明,肺部环境会随着年龄的增长而变得具有炎症性,并且这种炎症环境可以通过布洛芬来逆转。