Role of Oxidative and Nitrative Stress and Histone De-acetylation in Rhinovirus Induced Acute Exacerbations of COPD

氧化应激、硝基应激以及组蛋白去乙酰化在鼻病毒诱导的慢性阻塞性肺病急性加重中的作用

基本信息

  • 批准号:
    G0600879/1
  • 负责人:
  • 金额:
    $ 114.06万
  • 依托单位:
  • 依托单位国家:
    英国
  • 项目类别:
    Research Grant
  • 财政年份:
    2007
  • 资助国家:
    英国
  • 起止时间:
    2007 至 无数据
  • 项目状态:
    已结题

项目摘要

Chronic obstructive pulmonary disease (COPD) or smokers? lung is a growing problem and already one of the commonest causes of death and disability in the UK. COPD accounts for over #800 million in direct healthcare costs. Seventy percent of these costs are related to acute attacks. Acute attacks are also dreaded by COPD sufferers, as they lead to severe breathlessness, prolonged hospitalisation or death. Current therapies are not good at either treatment or prevention of acute attacks. New approaches to therapy are therefore urgently needed. COPD is associated with inflammation in the lung, which gets worse as the disease progresses. Acute attacks also involve inflammation in the lung but how this occurs is very poorly understood. Most acute attacks are caused by common cold viruses, which ?go to the chest?. We plan to carry out detailed studies of virus induced acute attacks of COPD, to understand the molecules switching on inflammation in the lung during these attacks. By identifying the molecules that increase lung inflammation during these attacks, we should be able to identify targets for the development of new therapies for both prevention and treatment of acute attack of COPD. So doing would greatly reduce distress suffered by COPD patients, as well as reducing mortality and health care costs.
慢性阻塞性肺疾病(COPD)或吸烟者?肺是一个日益严重的问题,已经是英国最常见的死亡和残疾原因之一。COPD占直接医疗费用的8亿多。其中70%的成本与急性攻击有关。COPD患者也害怕急性发作,因为它们会导致严重的呼吸困难,延长住院时间或死亡。目前的疗法在治疗或预防急性发作方面都不好。因此,迫切需要新的治疗方法。慢性阻塞性肺病与肺部炎症有关,随着疾病的进展,肺部炎症会变得更糟。急性发作也涉及肺部炎症,但对这种情况如何发生知之甚少。大多数急性发作是由普通感冒病毒引起的,哪种?去胸部?我们计划对病毒诱导的COPD急性发作进行详细研究,以了解在这些发作期间肺部炎症的分子。通过鉴定在这些发作期间增加肺部炎症的分子,我们应该能够确定用于预防和治疗COPD急性发作的新疗法的开发目标。这样做将大大减少COPD患者的痛苦,并降低死亡率和医疗费用。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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Sebastian Johnston其他文献

Soluble mediators derived from bronchial epithelium are able to drive Th2 differentiation in the context of rhinovirus infection
  • DOI:
    10.1186/2045-7022-3-s1-o1
  • 发表时间:
    2013-05-03
  • 期刊:
  • 影响因子:
    4.000
  • 作者:
    Heidi Makrinioti;Ross Walton;Nikolaos Papadopoulos;Michael Edwards;Aurica Telcian;David Cousins;Kerstin Wanke;Luminita Stanciu;Mubeccel Akdis;Spyridon Megremis;Cezmi Akdis;Sebastian Johnston
  • 通讯作者:
    Sebastian Johnston

Sebastian Johnston的其他文献

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{{ truncateString('Sebastian Johnston', 18)}}的其他基金

MICA: Effect of CRTH2 Antagonist OC459 on Response to Rhinovirus Challenge in Asthma
MICA:CRTH2 拮抗剂 OC459 对哮喘鼻病毒攻击反应的影响
  • 批准号:
    MR/M025330/1
  • 财政年份:
    2015
  • 资助金额:
    $ 114.06万
  • 项目类别:
    Research Grant
MICA: Phenotyping immune responses in asthma and respiratory infections - a systems approach to understanding changes from childhood to adulthood
MICA:哮喘和呼吸道感染的表型免疫反应——一种了解从儿童到成年变化的系统方法
  • 批准号:
    MR/L012693/1
  • 财政年份:
    2014
  • 资助金额:
    $ 114.06万
  • 项目类别:
    Research Grant
MRC-GSK Alliance: Mechanisms of interplay between allergy and viruses in asthma
MRC-GSK 联盟:哮喘中过敏和病毒之间相互作用的机制
  • 批准号:
    G1100238/1
  • 财政年份:
    2012
  • 资助金额:
    $ 114.06万
  • 项目类别:
    Research Grant
MRC-Asthma UK Centre in Allergic Mechanisms of Asthma (2)
MRC-Asthma 英国哮喘过敏机制中心 (2)
  • 批准号:
    G1000758-E01/2
  • 财政年份:
    2011
  • 资助金额:
    $ 114.06万
  • 项目类别:
    Research Grant
MRC-Asthma UK Centre in Allergic Mechanisms of Asthma (2)
MRC-Asthma 英国哮喘过敏机制中心 (2)
  • 批准号:
    G1000758-E01/1
  • 财政年份:
    2011
  • 资助金额:
    $ 114.06万
  • 项目类别:
    Research Grant
Mechanisms of Deficient Innate Immune Responses in Asthma
哮喘先天免疫反应缺陷的机制
  • 批准号:
    G0601236/1
  • 财政年份:
    2008
  • 资助金额:
    $ 114.06万
  • 项目类别:
    Research Grant

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    2024
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