Mechanism of basophil mediated immune modulation
嗜碱性粒细胞介导的免疫调节机制
基本信息
- 批准号:7897737
- 负责人:
- 金额:$ 23.55万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-07-22 至 2012-06-30
- 项目状态:已结题
- 来源:
- 关键词:AddressAftercareAllergensAllergicAllergic DiseaseAllergic inflammationAnimal ModelAntigensAsthmaBasophilsBiologyBlood CirculationCD4 Positive T LymphocytesCellsCharacteristicsDevelopmentDiseaseImmuneImmune responseImmunityImmunizationInfectionInfiltrationInflammation MediatorsInjection of therapeutic agentInterleukin-3Interleukin-4IntestinesLymphoidLymphoid TissueMediatingMusNematodaNippostrongylusParasitesParasitic infectionPathologyPeripheralPertussis ToxinPlayProcessProductionProteinsRecruitment ActivityReporterReportingRoleT-LymphocyteTestingTissuesadaptive immunitybasecell typechemokinechemokine receptorcytokineimmunoregulationin vivoinsightinterestlymph nodesmast cellmigrationnovelnovel strategiespreventpublic health relevance
项目摘要
DESCRIPTION (provided by applicant): Basophils are now recognized as critical effectors and immune modulators during Th2 mediated immune responses, such as allergic inflammations and parasite infections. Evidence suggests that basophils produce Th2 inducing factors including IL-4, the signature cytokine of Th2 immunity, thus inducing Th2 differentiation of activated naive CD4 T cells. However, given that basophils are mostly found in the circulation during steady- state conditions, how basophils contribute to the Th2 differentiation remain unknown. A recent study reported that basophils are transiently recruited into the draining lymph nodes upon allergen immunization, promoting Th2 differentiation. Consistent with this, we found transient basophil recruitment into the draining lymph node following parasite injection. Interestingly, IL-3 plays a crucial role in basophil recruitment as the recruitment was absent in IL-3 KO mice injected with parasites. Lymph node entry of adoptively transferred basophils was abolished after treatment with pertussis toxin, suggesting the involvement of chemokine/chemokine receptor interaction. Coinjection of OVA protein with parasites preferentially induces OVA-specific IL-4 producing T cell immunity within the draining lymph nodes, strongly suggesting that recruited basophils may be involved in mediating the Th2 immunity. Based on these results, we propose the hypothesis that IL-3 produced by activated T cells within the lymph nodes stimulates IL-3R+ target cells to recruit circulating basophils, thus promoting Th2 differentiation. Two specific aims will be tested to address the hypothesis. Aim #1 will test the contribution of IL-3 to the developing Th2 immunity via basophil recruitment. Aim #2 will define targets of IL-3 involved in basophil lymph node recruitment. Elucidating how basophils are recruited into tissues such as lymphoid or inflamed tissues will provide critical insights into understanding in vivo contribution of basophils to developing Th2 immunity as well as to basophil mediated pathology found in allergic inflammation including asthma. PUBLIC HEALTH RELEVANCE: Evidence indicating that basophils play critical roles in type 2 mediated immune responses found in allergic inflammations as well as parasitic infections is increasing. This proposal aims to investigate poorly defined mechanism by which basophils modulate immune responses. The results may allow us to better understand in vivo roles of these rare yet potent cells and to develop novel strategies to prevent basophil mediated pathology often found in allergic inflammations such as asthma.
描述(由申请人提供):嗜碱性粒细胞现在被认为是Th 2介导的免疫应答(如过敏性炎症和寄生虫感染)中的关键效应子和免疫调节剂。有证据表明,嗜碱性粒细胞产生Th 2诱导因子,包括IL-4,Th 2免疫的标志性细胞因子,从而诱导活化的初始CD 4 T细胞的Th 2分化。然而,鉴于嗜碱性粒细胞大多数在稳态条件下在循环中发现,嗜碱性粒细胞如何促进Th 2分化仍然是未知的。最近的一项研究报道,嗜碱性粒细胞在变应原免疫后瞬时募集到引流淋巴结中,促进Th 2分化。与此一致,我们发现在寄生虫注射后,引流淋巴结中有短暂的嗜碱性粒细胞募集。有趣的是,IL-3在嗜碱性粒细胞募集中起关键作用,因为在注射寄生虫的IL-3 KO小鼠中不存在募集。过继转移的嗜碱性粒细胞的淋巴结进入被废除后,百日咳毒素治疗,表明参与趋化因子/趋化因子受体相互作用。共注射卵蛋白与寄生虫优先诱导OVA特异性IL-4产生T细胞免疫引流淋巴结内,强烈表明,招募嗜碱性粒细胞可能参与介导的Th 2免疫。基于这些结果,我们提出了这样的假设,即淋巴结内活化的T细胞产生的IL-3刺激IL-3R+靶细胞募集循环嗜碱性粒细胞,从而促进Th 2分化。两个具体目标将进行测试,以解决假设。目的#1将测试IL-3通过嗜碱性粒细胞募集对Th 2免疫的发展的贡献。目的#2将定义参与嗜碱性粒细胞淋巴结募集的IL-3的靶点。阐明嗜碱性粒细胞是如何被募集到组织如淋巴或发炎组织中的,将为理解嗜碱性粒细胞对Th 2免疫的发展以及嗜碱性粒细胞介导的病理学在变应性炎症包括哮喘中的体内贡献提供重要的见解。公共卫生关系:越来越多的证据表明,嗜碱性粒细胞在过敏性炎症以及寄生虫感染中发现的2型介导的免疫应答中起关键作用。该建议旨在研究嗜碱性粒细胞调节免疫反应的机制。这些结果可能使我们能够更好地了解这些罕见但有效的细胞在体内的作用,并开发新的策略来预防嗜碱性粒细胞介导的病理学,这些病理学通常在过敏性炎症如哮喘中发现。
项目成果
期刊论文数量(7)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Cutting edge: basophils are transiently recruited into the draining lymph nodes during helminth infection via IL-3, but infection-induced Th2 immunity can develop without basophil lymph node recruitment or IL-3.
- DOI:10.4049/jimmunol.0902447
- 发表时间:2010-02-01
- 期刊:
- 影响因子:0
- 作者:Kim S;Prout M;Ramshaw H;Lopez AF;LeGros G;Min B
- 通讯作者:Min B
Epithelial cell-specific Act1 adaptor mediates interleukin-25-dependent helminth expulsion through expansion of Lin(-)c-Kit(+) innate cell population.
- DOI:10.1016/j.immuni.2012.03.021
- 发表时间:2012-05-25
- 期刊:
- 影响因子:32.4
- 作者:Kang Z;Swaidani S;Yin W;Wang C;Barlow JL;Gulen MF;Bulek K;Do JS;Aronica M;McKenzie AN;Min B;Li X
- 通讯作者:Li X
Mice that "conditionally" lack basophils, AT LAST.
“有条件”缺乏嗜碱性粒细胞的小鼠终于出现了。
- DOI:10.1172/jci44058
- 发表时间:2010
- 期刊:
- 影响因子:0
- 作者:Min,Booki
- 通讯作者:Min,Booki
Basophils, IgE, and autoantibody-mediated kidney disease.
- DOI:10.4049/jimmunol.1002648
- 发表时间:2011-06-01
- 期刊:
- 影响因子:0
- 作者:Bosch X;Lozano F;Cervera R;Ramos-Casals M;Min B
- 通讯作者:Min B
Basophils are the major producers of IL-4 during primary helminth infection.
- DOI:10.4049/jimmunol.1000940
- 发表时间:2011-03-01
- 期刊:
- 影响因子:0
- 作者:van Panhuys N;Prout M;Forbes E;Min B;Paul WE;Le Gros G
- 通讯作者:Le Gros G
{{
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 }}
Booki Min其他文献
Booki Min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('Booki Min', 18)}}的其他基金
miR-342, a novel glucocorticoid-responsive miRNA necessary for Foxp3+ regulatory T cell function
miR-342,一种新的糖皮质激素反应性 miRNA,是 Foxp3 调节 T 细胞功能所必需的
- 批准号:
10671943 - 财政年份:2023
- 资助金额:
$ 23.55万 - 项目类别:
Foxp3+ regulatory T cell-dependent treatment of allergic inflammation by glucocorticoids
Foxp3 调节性 T 细胞依赖性糖皮质激素治疗过敏性炎症
- 批准号:
10447598 - 财政年份:2020
- 资助金额:
$ 23.55万 - 项目类别:
Foxp3+ regulatory T cell-dependent treatment of allergic inflammation by glucocorticoids
Foxp3 调节性 T 细胞依赖性糖皮质激素治疗过敏性炎症
- 批准号:
10218031 - 财政年份:2020
- 资助金额:
$ 23.55万 - 项目类别:
Foxp3+ regulatory T cell-dependent treatment of allergic inflammation by glucocorticoids
Foxp3 调节性 T 细胞依赖性糖皮质激素治疗过敏性炎症
- 批准号:
9982786 - 财政年份:2019
- 资助金额:
$ 23.55万 - 项目类别:
The role of IL-27/Lag3 axis in regulating Foxp3+ regulatory T cell function
IL-27/Lag3轴在调节Foxp3调节性T细胞功能中的作用
- 批准号:
10264303 - 财政年份:2017
- 资助金额:
$ 23.55万 - 项目类别:
Mechanism of basophil mediated immune modulation
嗜碱性粒细胞介导的免疫调节机制
- 批准号:
7737907 - 财政年份:2009
- 资助金额:
$ 23.55万 - 项目类别:
相似海外基金
Life outside institutions: histories of mental health aftercare 1900 - 1960
机构外的生活:1900 - 1960 年心理健康善后护理的历史
- 批准号:
DP240100640 - 财政年份:2024
- 资助金额:
$ 23.55万 - 项目类别:
Discovery Projects
Development of a program to promote psychological independence support in the aftercare of children's homes
制定一项计划,促进儿童之家善后护理中的心理独立支持
- 批准号:
23K01889 - 财政年份:2023
- 资助金额:
$ 23.55万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Integrating Smoking Cessation in Tattoo Aftercare
将戒烟融入纹身后护理中
- 批准号:
10452217 - 财政年份:2022
- 资助金额:
$ 23.55万 - 项目类别:
Integrating Smoking Cessation in Tattoo Aftercare
将戒烟融入纹身后护理中
- 批准号:
10670838 - 财政年份:2022
- 资助金额:
$ 23.55万 - 项目类别:
Aftercare for young people: A sociological study of resource opportunities
年轻人的善后护理:资源机会的社会学研究
- 批准号:
DP200100492 - 财政年份:2020
- 资助金额:
$ 23.55万 - 项目类别:
Discovery Projects
Creating a National Aftercare Strategy for Survivors of Pediatric Cancer
为小儿癌症幸存者制定国家善后护理策略
- 批准号:
407264 - 财政年份:2019
- 资助金额:
$ 23.55万 - 项目类别:
Operating Grants
Aftercare of green infrastructure: creating algorithm for resolving human-bird conflicts
绿色基础设施的善后工作:创建解决人鸟冲突的算法
- 批准号:
18K18240 - 财政年份:2018
- 资助金额:
$ 23.55万 - 项目类别:
Grant-in-Aid for Early-Career Scientists
Development of an aftercare model for children who have experienced invasive procedures
为经历过侵入性手术的儿童开发善后护理模型
- 批准号:
17K12379 - 财政年份:2017
- 资助金额:
$ 23.55万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Development of a Comprehensive Aftercare Program for children's self-reliance support facility
为儿童自力更生支持设施制定综合善后护理计划
- 批准号:
17K13937 - 财政年份:2017
- 资助金额:
$ 23.55万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
Project#2 Extending Treatment Effects Through an Adaptive Aftercare Intervention
项目
- 批准号:
8742767 - 财政年份:2014
- 资助金额:
$ 23.55万 - 项目类别: