Airways eosinophils as antigen-presenting cells-asthma

气道嗜酸性粒细胞作为抗原呈递细胞-哮喘

基本信息

  • 批准号:
    6632607
  • 负责人:
  • 金额:
    $ 38.25万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2001
  • 资助国家:
    美国
  • 起止时间:
    2001-09-30 至 2006-05-31
  • 项目状态:
    已结题

项目摘要

Description (provided by applicant): Studies will investigate the ability of eosinophils to serve as antigen-presenting cells that contribute to propagating lymphocyte-dependent, IgE-mediated response to inhaled antigens in the respiratory tract. Eosinophils are prominent cellular components of allergic airway responses. While many cells function as antigen-presenting cells, eosinophils have distinct capabilities within the airway. First, eosinophils are present in the airway lumina of asthmatics; and these eosinophils in vivo express requisite class II MHC proteins and critical lymphocyte costimulatory proteins. Second, eosinophils contain preformed stores of cytokines that may be rapidly mobilized for extra cellular release to modulate lymphocyte-dependent responses. Third, unlike B cells and dendritic cells that are capable of presenting soluble protein antigens, eosinophils, like macrophages, are especially able to degrade particulate antigens. Alveolar macrophages are poor antigen-presenting cells. In contrast, eosinophils could present peptides derived from particulate inhaled allergens. Fourth, antibodies of several classes, by Fc receptor-mediated mechanisms, can dramatically enhance antigen uptake and presentation by antigen-presenting cells. Eosinophils with their IgE, IgA, and IgG antibodies receptors are well suited to internalize and present allergens recognized by allergen-specific IgE, IgA, and IgG antibodies present in the respiratory tract. Fifth, eosinophil trafficking from the airway lumen into lymphocytes provides a mechanism for antigens inhaled into the airways to be processed and transported into tissues for presentation to lymphocytes. Hypotheses are that eosinophils are effective at presenting inhaled antigens to lymphocytes, that this eosinophil antigen processing and trafficking occur in vivo within the airways, that eosinophil high affinity IgE receptors function to enhance eosinophil antigen presentation of allergens, and that antigen presentation by eosinophils, perhaps based on their release of preformed, cytokines, skews Th2-mediated responses to inhaled antigens. Studies aim to define the capacity of human eosinophils in vitro to function as antigen-presenting cells and to define the role of eosinophil IgE receptors in facilitating antigen presentation by eosinophils. These studies of eosinophils active in asthma focus on the roles of eosinophils in propagating the chronic airway inflammation of asthma. Roles for eosinophils as antigen-presenting cells in sustaining allergic responses to inhaled particulate allergens would provide insights into the characteristically chronic nature of allergic diseases.
描述(由申请人提供):研究将调查 嗜酸性粒细胞作为抗原呈递细胞, 增殖淋巴细胞依赖性IgE介导的对吸入抗原的应答, 呼吸道。嗜酸性粒细胞是重要的细胞成分, 过敏性气道反应虽然许多细胞的功能是抗原呈递 嗜酸性粒细胞在气道内具有独特的功能。第一、 嗜酸性粒细胞存在于哮喘患者的气道腔中;并且这些嗜酸性粒细胞 体内嗜酸性粒细胞表达必需的II类MHC蛋白, 淋巴细胞共刺激蛋白。其次,嗜酸性粒细胞含有预先形成的 细胞因子的储存,可被迅速动员以释放到细胞外 调节淋巴细胞依赖性反应。第三,与B细胞和 能够呈递可溶性蛋白抗原的树突细胞, 嗜酸性粒细胞,像巨噬细胞,特别能够降解颗粒 抗原肺泡巨噬细胞是不良的抗原呈递细胞。在 相比之下,嗜酸性粒细胞可以呈递来自吸入颗粒物的肽, 过敏原第四,几类抗体,通过Fc受体介导 机制,可以显着提高抗原的摄取和呈递, 抗原呈递细胞嗜酸性粒细胞及其IgE、伊加和IgG抗体 受体非常适合于内化和呈递被 过敏原特异性IgE,伊加和IgG抗体存在于呼吸道 道。第五,嗜酸性粒细胞从气道腔运输到淋巴细胞 提供了一种机制,用于处理吸入气道的抗原, 转运到组织中呈递给淋巴细胞。假设是, 嗜酸性粒细胞能有效地将吸入的抗原呈递给淋巴细胞, 这种嗜酸性粒细胞抗原的加工和运输在体内发生在 气道,嗜酸性粒细胞高亲和力IgE受体的功能,以增强 嗜酸性粒细胞抗原呈递过敏原,和抗原呈递 嗜酸性粒细胞,也许是基于它们释放的预先形成的细胞因子, Th 2介导的对吸入抗原的应答。研究旨在确定 体外人嗜酸性粒细胞作为抗原呈递细胞的能力 并确定嗜酸性粒细胞IgE受体在促进抗原 嗜酸性粒细胞的表现。这些关于嗜酸性粒细胞在哮喘中的活性的研究 重点研究嗜酸性粒细胞在慢性气道炎症中的作用 哮喘的炎症。嗜酸性粒细胞作为抗原提呈细胞的作用 对吸入颗粒过敏原的持续过敏反应将提供 深入了解过敏性疾病的慢性特征。

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 }}

PETER F WELLER其他文献

PETER F WELLER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('PETER F WELLER', 18)}}的其他基金

Human Eosinophils: Mechanisms of Functioning
人类嗜酸性粒细胞:功能机制
  • 批准号:
    9242550
  • 财政年份:
    2015
  • 资助金额:
    $ 38.25万
  • 项目类别:
Human Eosinophils: Mechanisms of Functioning
人类嗜酸性粒细胞:功能机制
  • 批准号:
    7878373
  • 财政年份:
    2009
  • 资助金额:
    $ 38.25万
  • 项目类别:
Airways Eosinophils as Antigen-presenting Cells in Asthma
气道嗜酸性粒细胞作为哮喘中的抗原呈递细胞
  • 批准号:
    7921759
  • 财政年份:
    2009
  • 资助金额:
    $ 38.25万
  • 项目类别:
Multi-Laser Flow Cytometer
多激光流式细胞仪
  • 批准号:
    6730722
  • 财政年份:
    2004
  • 资助金额:
    $ 38.25万
  • 项目类别:
MULTI-LASER FLOW CYTOMETER: CANCER: BREAST, PROSTATE
多激光流式细胞仪:癌症:乳腺癌、前列腺癌
  • 批准号:
    6973415
  • 财政年份:
    2004
  • 资助金额:
    $ 38.25万
  • 项目类别:
MULTI-LASER FLOW CYTOMETER: INFECTIOUS DIS, HERPE VIRUS, HCV
多激光流式细胞仪:传染性 DIS、疱疹病毒、HCV
  • 批准号:
    6973417
  • 财政年份:
    2004
  • 资助金额:
    $ 38.25万
  • 项目类别:
MULTI-LASER FLOW CYTOMETER: HIV
多激光流式细胞仪:HIV
  • 批准号:
    6973414
  • 财政年份:
    2004
  • 资助金额:
    $ 38.25万
  • 项目类别:
MULTI-LASER FLOW CYTOMETER: LUNG, AIRWAY & ALLERGIC INFLAMMATION
多激光流式细胞仪:肺、气道
  • 批准号:
    6973416
  • 财政年份:
    2004
  • 资助金额:
    $ 38.25万
  • 项目类别:
Eosinophils in Pulmonary Fibrosis
肺纤维化中的嗜酸性粒细胞
  • 批准号:
    6850807
  • 财政年份:
    2002
  • 资助金额:
    $ 38.25万
  • 项目类别:
Eosinophils in Pulmonary Fibrosis
肺纤维化中的嗜酸性粒细胞
  • 批准号:
    6731179
  • 财政年份:
    2002
  • 资助金额:
    $ 38.25万
  • 项目类别:

相似海外基金

Analysis of expression of Cd antigens in retinoblastoma, and its application for disease classification and therapeutic strategy
视网膜母细胞瘤中Cd抗原的表达分析及其在疾病分类和治疗策略中的应用
  • 批准号:
    25670726
  • 财政年份:
    2013
  • 资助金额:
    $ 38.25万
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了