Mechanisms of Deficient Innate Immune Responses in Asthma

哮喘先天免疫反应缺陷的机制

基本信息

  • 批准号:
    G0601236/1
  • 负责人:
  • 金额:
    $ 155.42万
  • 依托单位:
  • 依托单位国家:
    英国
  • 项目类别:
    Research Grant
  • 财政年份:
    2008
  • 资助国家:
    英国
  • 起止时间:
    2008 至 无数据
  • 项目状态:
    已结题

项目摘要

Asthma is the most common chronic respiratory disease in the UK. The majority of healthcare costs are related to acute attacks. Acute attacks are also dreaded by asthma sufferers, as they lead to severe breathlessness, hospitalisation or death. Current therapies are not good at either treatment or prevention of acute attacks. New approaches to therapy are therefore urgently needed. Asthma attacks are caused by common cold viruses, which ?go to the chest?, some are also made worse by chronic bacterial colonisation which can be ?reactivated? during acute attacks. We have discovered asthmatics have weak immune responses to viral and bacterial infections, accounting for their increased susceptibility to these infections. We plan to carry out detailed studies of anti-viral and anti-bacterial immunity in lung cells from adults with asthma, to identify the molecules deficient in switching on immune responses in the lung during these attacks. We will also study different forms of asthma to see how widespread these deficiencies are, and will study children through from birth to 6 years of age, to see when these deficiencies develop. Finally we will see if the deficiencies are detected in blood tests so they can be more easily identified.By identifying the molecules that are deficient 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 asthma. So doing would greatly reduce distress suffered by asthma patients, as well as reducing mortality and health care costs.
哮喘是英国最常见的慢性呼吸道疾病。大部分医疗费用与急性发作有关。哮喘患者也害怕急性发作,因为它们会导致严重的呼吸困难,住院治疗或死亡。目前的疗法既不擅长治疗也不擅长预防急性发作。因此,迫切需要新的治疗方法。哮喘发作是由普通感冒病毒引起的,哪种?去胸部?有些人还恶化的慢性细菌定植,这可能是?重新激活?急性发作时。我们发现哮喘患者对病毒和细菌感染的免疫反应较弱,这是他们对这些感染易感性增加的原因。我们计划在成人哮喘患者的肺细胞中进行抗病毒和抗细菌免疫的详细研究,以确定在这些攻击期间肺中启动免疫反应的分子缺陷。我们还将研究不同形式的哮喘,看看这些缺陷有多普遍,并将研究从出生到6岁的儿童,看看这些缺陷何时发展。最后,我们将看看是否在血液测试中检测到这些缺陷,以便更容易地识别它们。通过识别在这些发作期间缺乏的分子,我们应该能够确定开发新疗法的目标,用于预防和治疗哮喘急性发作。这样做将大大减少哮喘患者所遭受的痛苦,并降低死亡率和医疗保健费用。

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)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

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

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ 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:
    $ 155.42万
  • 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:
    $ 155.42万
  • 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:
    $ 155.42万
  • 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:
    $ 155.42万
  • 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:
    $ 155.42万
  • 项目类别:
    Research Grant
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
  • 批准号:
    G0600879/1
  • 财政年份:
    2007
  • 资助金额:
    $ 155.42万
  • 项目类别:
    Research Grant

相似国自然基金

DnaJ蛋白PDP10(PSI Deficient Protein 10)调控光系统I生物发生和功能的研究
  • 批准号:
    31970291
  • 批准年份:
    2019
  • 资助金额:
    58.0 万元
  • 项目类别:
    面上项目
拟南芥PDP2(Photosystem I Deficient Protein 2)蛋白参与光系统I生物发生的分子机理研究
  • 批准号:
    31300994
  • 批准年份:
    2013
  • 资助金额:
    23.0 万元
  • 项目类别:
    青年科学基金项目

相似海外基金

Generation of RORgt+ Innate lymphpid cell deficient mouse
RORgt 先天淋巴细胞缺陷小鼠的产生
  • 批准号:
    25670228
  • 财政年份:
    2013
  • 资助金额:
    $ 155.42万
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
Innate antiviral response and predisposition to neoplasia in IRF-5 deficient mous
IRF-5 缺陷小鼠的先天抗病毒反应和肿瘤易感性
  • 批准号:
    8082049
  • 财政年份:
    2010
  • 资助金额:
    $ 155.42万
  • 项目类别:
Innate antiviral response and predisposition to neoplasia in IRF-5 deficient mous
IRF-5 缺陷小鼠的先天抗病毒反应和肿瘤易感性
  • 批准号:
    7879743
  • 财政年份:
    2009
  • 资助金额:
    $ 155.42万
  • 项目类别:
Innate antiviral response and predisposition to neoplasia in IRF-5 deficient mous
IRF-5 缺陷小鼠的先天抗病毒反应和肿瘤易感性
  • 批准号:
    7436171
  • 财政年份:
    2006
  • 资助金额:
    $ 155.42万
  • 项目类别:
Innate antiviral response and predisposition to neoplasia in IRF-5 deficient mous
IRF-5 缺陷小鼠的先天抗病毒反应和肿瘤易感性
  • 批准号:
    7893111
  • 财政年份:
    2006
  • 资助金额:
    $ 155.42万
  • 项目类别:
Innate antiviral response and predisposition to neoplasia in IRF-5 deficient mous
IRF-5 缺陷小鼠的先天抗病毒反应和肿瘤易感性
  • 批准号:
    7252075
  • 财政年份:
    2006
  • 资助金额:
    $ 155.42万
  • 项目类别:
Innate antiviral response and predisposition to neoplasia in IRF-5 deficient mous
IRF-5 缺陷小鼠的先天抗病毒反应和肿瘤易感性
  • 批准号:
    7149544
  • 财政年份:
    2006
  • 资助金额:
    $ 155.42万
  • 项目类别:
Innate antiviral response and predisposition to neoplasia in IRF-5 deficient mous
IRF-5 缺陷小鼠的先天抗病毒反应和肿瘤易感性
  • 批准号:
    7665044
  • 财政年份:
    2006
  • 资助金额:
    $ 155.42万
  • 项目类别:
Phytoestrogens and innate immunity in ER deficient mice
ER 缺陷小鼠的植物雌激素和先天免疫
  • 批准号:
    6647790
  • 财政年份:
    2002
  • 资助金额:
    $ 155.42万
  • 项目类别:
Phytoestrogens and innate immunity in ER deficient mice
ER 缺陷小鼠的植物雌激素和先天免疫
  • 批准号:
    6575694
  • 财政年份:
    2002
  • 资助金额:
    $ 155.42万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了