Human MAIT celis in airway mucosal immune responses to intracellular infections

人 MAIT 细胞在气道粘膜对细胞内感染的免疫反应中的作用

基本信息

  • 批准号:
    8286891
  • 负责人:
  • 金额:
    $ 241.64万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2011
  • 资助国家:
    美国
  • 起止时间:
    2011-07-01 至 2016-06-30
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): The human airway is a complex immune organ, reflecting its central role in the host response to airborne infection. Innate T cells found within the airway have the potential to play a critical role in the recognition of these pathogens, in their control, and in the acquisition of adaptive immunity. Human mucosal associated invariant T (MAIT) cells are a unique T cell population found in all humans that are characterized by the use of a semi-invariant T cell receptor (TCR; Va7.2), dependence on the non-classical (HLA-lb) molecule MRI, and their rapid effector function. We have recently found MAIT cells to be capable of the recognition of bacterially-infected epithelial cells, and to be highly enriched in the human airway and lung parenchyma. Furthermore, in an analysis of the role of MAIT cells in those infected with Mycobacterium tuberculosis (Mtb), we found these cells to be virtually absent in those with active but not latent tuberculosis. As a result, the location of MAIT cells in the human airway, in conjunction with their ability to rapidly respond to bacterially infected epithelial cells positions these cells to play a critical role in the control of intracellular infection. The specific aims of this proposal are designed to delineate the role of these cells in the human host response to airborne infection. First, while we have found that MRI-restricted MAIT cells are capable of recognizing a broad array of pathogens, the diversity of ligand and/or pathogen recognition is not known. As a result, in the first aim the full spectrum of pathogens recognized by MAIT cells will be characterized with regard to TCR usage. Second, we have found that human primary lung epithelial cells can produce INOS both in response to IFN-gamma as well as direct T cell contact. Consequently, in the second aim we will determine the contribution of MAIT cells to the production of epithelial iNOS and consequent bacterial control. Finally, in our analysis of human airway immune cells, we have observed the presence of MAIT cells in the absence of DC. Consequently, we postulate that one function of MAIT cells is to "license" lung epithelial cells resulting in the recruitment and maturation of DC. The third aim will determine the relationship of MAIT cells with airway epithelium and dendritic cells. PUBLIC HEALH RELEVANCE (from applicant): Airborne Infections due to intracellular bacteria are a frequent and severe cause of morbidity and mortality worldwide. The airway contains a number of immune effector cells, yet their role in the recognition and control of intracellular bacteria is poorly understood. This application will focus on an innate class of T cells termed mucosal associated invariant T cells (MAIT) that are highly enriched in the human airway.
描述(由申请人提供):人体气道是一个复杂的免疫器官,反映了其在宿主对空气传播感染的反应中的核心作用。在气道内发现的先天性T细胞有可能在识别这些病原体、控制它们以及获得适应性免疫中发挥关键作用。人粘膜相关不变T(MAIT)细胞是在所有人中发现的独特T细胞群,其特征在于使用半不变T细胞受体(TCR; Va 7.2)、依赖于非经典(HLA-Ib)分子MRI以及它们的快速效应子功能。我们最近发现MAIT细胞能够识别细菌感染的上皮细胞,并且在人气道和肺实质中高度富集。此外,在分析MAIT细胞在结核分枝杆菌(Mtb)感染者中的作用时,我们发现这些细胞在活动性而非潜伏性结核病患者中几乎不存在。因此,MAIT细胞在人气道中的位置,连同它们快速响应细菌感染的上皮细胞的能力,使这些细胞在控制细胞内感染中发挥关键作用。该建议的具体目标是描述这些细胞在人类宿主对空气传播感染的反应中的作用。首先,虽然我们已经发现MRI限制性MAIT细胞能够识别广泛的病原体,但配体和/或病原体识别的多样性尚不清楚。因此,在第一个目标中,MAIT细胞识别的病原体的全谱将关于TCR使用来表征。第二,我们发现人原代肺上皮细胞可以产生INOS以响应IFN-γ以及直接的T细胞接触。因此,在第二个目标中,我们将确定MAIT细胞对上皮iNOS的产生和随后的细菌控制的贡献。最后,在我们对人气道免疫细胞的分析中,我们观察到在不存在DC的情况下MAIT细胞的存在。因此,我们推测MAIT细胞的一个功能是“许可”肺上皮细胞,导致DC的募集和成熟。第三个目标是确定MAIT细胞与气道上皮细胞和树突状细胞的关系。 公共卫生相关性(来自申请人):由于细胞内细菌引起的空气传播感染是全球范围内发病率和死亡率的常见和严重原因。气道含有大量的免疫效应细胞,但它们在识别和控制细胞内细菌中的作用知之甚少。本申请将集中于被称为粘膜相关不变T细胞(MAIT)的先天性T细胞类别,其在人气道中高度富集。

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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Marielle C. Gold其他文献

Effective Inhibition of Kb- and Db-Restricted Antigen Presentation in Primary Macrophages by Murine Cytomegalovirus
鼠巨细胞病毒有效抑制原代巨噬细胞中 Kb 和 Db 限制性抗原的呈递
  • DOI:
  • 发表时间:
    2003
  • 期刊:
  • 影响因子:
    5.4
  • 作者:
    D. Lopiccolo;Marielle C. Gold;D. Kavanagh;M. Wagner;U. Koszinowski;A. Hill
  • 通讯作者:
    A. Hill
The Multiple Immune-Evasion Genes of Murine Cytomegalovirus Are Not Redundant
鼠巨细胞病毒的多个免疫逃避基因并非冗余
  • DOI:
  • 发表时间:
    2001
  • 期刊:
  • 影响因子:
    15.3
  • 作者:
    D. Kavanagh;Marielle C. Gold;M. Wagner;U. Koszinowski;A. Hill
  • 通讯作者:
    A. Hill
The Murine Cytomegalovirus Immunomodulatory Gene m152 Prevents Recognition of Infected Cells by M45-Specific CTL But Does Not Alter the Immunodominance of the M45-Specific CD8 T Cell Response In Vivo1
鼠巨细胞病毒免疫调节基因 m152 阻止 M45 特异性 CTL 识别感染细胞,但不会改变体内 M45 特异性 CD8 T 细胞反应的免疫优势1
  • DOI:
  • 发表时间:
    2002
  • 期刊:
  • 影响因子:
    4.4
  • 作者:
    Marielle C. Gold;M. Munks;M. Wagner;U. Koszinowski;A. Hill;S. Fling
  • 通讯作者:
    S. Fling
Co-dependents: MR1-restricted MAIT cells and their antimicrobial function
共依赖细胞:MR1 限制的黏膜相关不变 T 细胞及其抗菌功能
  • DOI:
    10.1038/nrmicro2918
  • 发表时间:
    2012-11-26
  • 期刊:
  • 影响因子:
    103.300
  • 作者:
    Marielle C. Gold;David M. Lewinsohn
  • 通讯作者:
    David M. Lewinsohn
T Cell Response In Vivo Immunodominance of the M 45-Specific CD 8 CTL But Does Not Alter the Recognition of Infected Cells by M 45-Specific Prevents m 152 Immunomodulatory Gene The Murine Cytomegalovirus
M 45 特异性 CD 8 CTL 的体内 T 细胞反应,但不改变 M 45 特异性对感染细胞的识别,可阻止 m 152 免疫调节基因 鼠巨细胞病毒
  • DOI:
  • 发表时间:
    2002
  • 期刊:
  • 影响因子:
    0
  • 作者:
    U. Koszinowski;A. Hill;S. Fling;Marielle C. Gold;M. Munks;M. Wagner
  • 通讯作者:
    M. Wagner

Marielle C. Gold的其他文献

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{{ truncateString('Marielle C. Gold', 18)}}的其他基金

Human MAIT celis in airway mucosal immune responses to intracellular infections
人 MAIT 细胞在气道粘膜对细胞内感染的免疫反应中的作用
  • 批准号:
    8493988
  • 财政年份:
    2011
  • 资助金额:
    $ 241.64万
  • 项目类别:
Innate Immune Effectors in Early Immune Response to Mycobacterium Tuberculosis
结核分枝杆菌早期免疫反应中的先天免疫效应器
  • 批准号:
    8391646
  • 财政年份:
    2011
  • 资助金额:
    $ 241.64万
  • 项目类别:
Human MAIT celis in airway mucosal immune responses to intracellular infections
人 MAIT 细胞在气道粘膜对细胞内感染的免疫反应中的作用
  • 批准号:
    8692637
  • 财政年份:
    2011
  • 资助金额:
    $ 241.64万
  • 项目类别:
Human MAIT celis in airway mucosal immune responses to intracellular infections
人 MAIT 细胞在气道粘膜对细胞内感染的免疫反应中的作用
  • 批准号:
    8180933
  • 财政年份:
    2011
  • 资助金额:
    $ 241.64万
  • 项目类别:
Innate Immune Effectors in Early Immune Response to Mycobacterium Tuberculosis
结核分枝杆菌早期免疫反应中的先天免疫效应器
  • 批准号:
    8598038
  • 财政年份:
    2011
  • 资助金额:
    $ 241.64万
  • 项目类别:
Innate Immune Effectors in Early Immune Response to Mycobacterium Tuberculosis
结核分枝杆菌早期免疫反应中的先天免疫效应器
  • 批准号:
    8762416
  • 财政年份:
    2011
  • 资助金额:
    $ 241.64万
  • 项目类别:
Innate Immune Effectors in Early Immune Response to Mycobacterium Tuberculosis
结核分枝杆菌早期免疫反应中的先天免疫效应器
  • 批准号:
    8243325
  • 财政年份:
    2011
  • 资助金额:
    $ 241.64万
  • 项目类别:
Mechanisms of recognition by Mycobacterium tuberculosis-reactive thymocytes
结核分枝杆菌反应性胸腺细胞的识别机制
  • 批准号:
    7882010
  • 财政年份:
    2010
  • 资助金额:
    $ 241.64万
  • 项目类别:
Mechanisms of recognition by Mycobacterium tuberculosis-reactive thymocytes
结核分枝杆菌反应性胸腺细胞的识别机制
  • 批准号:
    8306184
  • 财政年份:
    2010
  • 资助金额:
    $ 241.64万
  • 项目类别:
Mechanisms of recognition by Mycobacterium tuberculosis-reactive thymocytes
结核分枝杆菌反应性胸腺细胞的识别机制
  • 批准号:
    8510549
  • 财政年份:
    2010
  • 资助金额:
    $ 241.64万
  • 项目类别:

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