Mucosal Immunology Course & Symposium (MICS)
粘膜免疫学课程
基本信息
- 批准号:9195544
- 负责人:
- 金额:$ 0.4万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2016
- 资助国家:美国
- 起止时间:2016-07-01 至 2017-06-30
- 项目状态:已结题
- 来源:
- 关键词:AddressAntigensAreaAsthmaAwardB-LymphocytesBioinformaticsBiotechnologyBloodCattleCeliac DiseaseCollaborationsCommittee MembersCommunicationConsultCritiquesCuesDataDendritic CellsDevelopmentDietDiet and NutritionDisciplineDiseaseDrug IndustryEcologyEnvironmentEpithelial CellsExtrinsic asthmaEyeFoodFood HypersensitivityFosteringGenitourinary systemHIVHealthHumanHypersensitivityImmune responseImmune systemImmunityImmunobiologyImmunoglobulin AImmunoglobulin-Secreting CellsImmunologistImmunologyIncubatorsInfectionInflammatory Bowel DiseasesInternationalKnowledgeLower respiratory tract structureLungLymphoidLymphoid CellLymphoid TissueMedicalMicrobeMicrobiologyMilkMucosal ImmunityNatural ImmunityNatureOralOrganProbioticsPubMedPublishingResearchResearch PersonnelRoleScienceScientistSecretory Immunoglobulin ASiteSpleenStomachSurfaceSurveysSystems DevelopmentT-LymphocyteTherapeuticTimeTissuesTransplantationTravelUpper digestive tract structureUpper respiratory tractVaccinationWheatWorkabstractingbasecostcytokineeducation researchgut microbiotainterestlymph nodesmacrophagemeetingsmicrobialmicrobiomemicrobiotamonocytemucosal vaccinepathogenpostersprogramsrapid growthresponsesymposiumtrenduptake
项目摘要
As the degree of interest in mucosal immunology continues its upswing, the SMI has decided to
initiate a second set of biennial meetings to be called “Mucosal Immunology Course and
Symposium” that will be held in even‐numbered years. These meetings will include a full day
course aimed mainly at trainees preceding the main meeting, which will be organized as a
symposium emphasizing a prominent and active area from within the broad area of mucosal
immunology. The first SMI‐sponsored MICS meeting will be held in Toronto from July 26‐30,
2016. The content of this meeting will focus on the educational theme of “Microbiota and
Mucosal Immunity: Rules of Engagement in Health and Disease”. The breadth of research into
the nature and function of the commensal microbiota has surged in recent years. Most of the
human microbiota is resident at one of the major mucosal surfaces, including the
gastrointestinal tract, the upper and lower respiratory tract, and the genitourinary system. Thus
there is a natural scientific interface between studies of the microbiota and studies of mucosal
immunology. Scientific sessions will promote excellence in research and education across many
areas of mucosal immunology and microbiota studies and will foster increased communication
and scientific collaboration among immunologists and microbiota researchers.
MICS 2016, co‐chaired by Drs. Ifor Williams, Phil Smith, Dana Philpott, Ken Croitoru, and
Gerard Eberl, will deliver another exciting program of wide interest to mucosal immunologists.
The meeting includes 17 keynote and plenary speakers who will present new information in
areas relating to influence of the microbiota on asthma and allergies, secretory IgA and the
mucosal microbiota, the microbiota and gut immune system development, intestinal microbiota
and inflammatory bowel disease, mucosal immunity to urogenital microbiota and therapeutic
modulation of the human gut microbiota. These sessions will be enhanced by an additional 20
invited speakers who will chair abstract‐driven sessions on antigen uptake, asthma and atopic
disease, bioinformatics analysis of microbiota, celiac disease, dendritic cells, diet, nutrition and
microbiota, effector T cells and cytokines, epithelial cells in innate immunity, fecal microbiota
transplantation, food allergy, gastric microbiota, genitourinary microbiota, HIV, IgA responses
to microbiota, inflammatory bowel disease, innate immune responses, innate lymphoid cells,
intestinal microbiota, microbial ecology of mucosal surfaces, monocytes and macrophages,
mucosal B cells, mucosal infections, mucosal tolerance, mucosal vaccines and probiotics. The
educational content of MICS 2016 was developed by SMI's International Planning Committee,
which is comprised of leaders in the mucosal immunology field. As experts, committee
members engaged in discussions in which topics are identified and developed into sessions.
Committee members drew from their extensive knowledge, and also consulted membership
surveys and conducted after previous SMI meetings to create a program that addresses timely
topics in mucosal immunology with a strong emphasis on interactions between the mucosal
immune system and the microbiota resident at mucosal surfaces. In addition to highlighting the
best science, MICS 2016 will also be an incubator for developing scientists and practitioners
alike to meet with one another along with representatives of relevant biotechnology and
pharmaceutical industry. The meeting includes 3 days of oral abstract presentations and 2
evening poster sessions to give young investigators the change to have their work presented
and critiqued. SMI takes a specific interest in the development of young investigators and
provides travel awards to them to supplement their costs to attend the meeting.
随着人们对黏膜免疫学的兴趣程度继续上升,美国食品和药物管理局已决定继续。
启动一套新的两年一次的国际会议,被称为“粘膜免疫学”课程。
研讨会将在偶数年举行一次。这些会议将包括一整天的时间。
本课程主要是针对大会主要会议之前的实习生,会议将作为一个整体进行组织。
座谈会强调从胃粘膜的广泛区域内寻找一个突出的区域和活跃的区域。
免疫学。第一次由SMI赞助的MICS会议将于7月26日至30日在多伦多市中心举行。
2016年,本次会议的主要内容内容将集中在新的教育主题--《微生物区系》和《生物多样性》。
粘膜免疫:《健康与疾病》的参与规则。将其研究的广度扩大到
近几年来,全球共生微生物群的性质和功能都有了很大的提高。
人类的微生物群至少是一种主要的粘膜表面的居民生物,包括动物。
胃肠道,包括上呼吸道和下呼吸道,控制着整个泌尿生殖系统。
在对微生物区系的研究和对粘膜组织的研究之间,存在着一种天然的、科学的界面。
免疫学。科学会议将在许多国家促进他们在研究和教育领域的卓越成就。
包括黏膜免疫学和微生物群研究在内的领域将进一步促进更多的信息交流。
此外,还加强了免疫学家和微生物群研究人员之间的科学和技术合作。
MICS在2016年,由威廉博士、菲尔·史密斯博士、达纳·菲尔波特博士、肯·克罗伊托鲁博士、约翰·克洛托鲁博士共同主持。
Gerard和Eberl还将为黏膜和免疫学家提供另一个令人兴奋的、引起广泛兴趣的新程序。
本次会议将包括17位主旨发言人和3位全体演讲者,他们将在会议上介绍新的信息。
与微生物区系对儿童哮喘和过敏症的影响、分泌性免疫球蛋白A分泌和免疫球蛋白相关的领域。
黏膜微生物区系是最主要的微生物区系,肠道微生物区系是肠道免疫系统发育的主要微生物区系。
炎症性肠病、粘膜免疫、泌尿生殖系统、微生物区系和治疗性疾病。
对人类肠道和微生物区系的调制能力。在这些会议上,我们将通过增加20亿美元来加强这些会议。
受邀的演讲者将主持一个抽象驱动的会议,主题是抗原摄取、哮喘和特应性。
疾病,包括微生物区系、乳酸菌病、树突状细胞、饮食、营养和营养等的分析研究。
微生物群是T细胞的效应者,参与细胞因子的作用,上皮性细胞参与先天免疫,粪便和微生物群。
移植、食物过敏、胃肠道微生物区系、泌尿生殖道微生物区系、艾滋病毒、免疫球蛋白A免疫应答。
对于微生物区系,炎症性肠病,先天免疫反应,先天免疫反应,先天免疫细胞,
肠道微生物区系,包括粘膜表面、单核细胞和巨噬细胞的微生物生态系统。
粘膜免疫B细胞、黏膜免疫感染、黏膜免疫耐受、黏膜免疫疫苗和益生菌。
2016年MICS的教育内容指南是由SMI的全球国际教育规划委员会共同开发的。
该委员会由世界黏膜免疫领域的领导者组成。作为全球专家,该委员会表示。
成员们还参与了讨论,在这些讨论中,他们确定了一些主题,并将其发展为两个会议。
委员们汲取了他们广泛的专业知识,他们也征求了委员们的意见。
在之前的几次SMI会议之后进行的调查和调查都是为了创建一个解决问题的及时解决问题的计划。
主题集中在粘膜组织免疫学上,特别强调组织与粘膜组织之间的相互作用。
免疫系统控制和控制微生物群,使其停留在粘膜表面。除了突出其重要性外,还包括
2016年的最佳科学,MICS也将成为培养优秀科学家和科技从业者的全球孵化器。
我们将陆续与中国相关生物技术公司和企业的代表会面。
制药和工业。这次会议包括为期3天的口头和摘要演讲,以及第二次会议。
晚上的海报会议是为了让年轻的调查人员了解他们已经提交的最新工作的变化。
并受到了批评。SMI对中国年轻科技调查员的健康发展给予了特殊的关注。
提供旅行和奖励,以帮助他们补充他们参加会议的费用。
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 }}
IFOR R WILLIAMS其他文献
IFOR R WILLIAMS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('IFOR R WILLIAMS', 18)}}的其他基金
CCR6 Regulation of Intestinal T Lymphocyte Development
CCR6 对肠道 T 淋巴细胞发育的调节
- 批准号:
6875743 - 财政年份:2004
- 资助金额:
$ 0.4万 - 项目类别:
CCR6 Regulation of Intestinal T Lymphocyte Development
CCR6 对肠道 T 淋巴细胞发育的调节
- 批准号:
7216199 - 财政年份:2004
- 资助金额:
$ 0.4万 - 项目类别:
Regulation of Organized Intestinal Lymphoid Tissues by TRANCE/RANKL
TRANCE/RANKL 对有组织肠淋巴组织的调节
- 批准号:
7732048 - 财政年份:2004
- 资助金额:
$ 0.4万 - 项目类别:
Regulation of Organized Intestinal Lymphoid Tissues by TRANCE/RANKL
TRANCE/RANKL 对有组织肠淋巴组织的调节
- 批准号:
8137918 - 财政年份:2004
- 资助金额:
$ 0.4万 - 项目类别:
CCR6 Regulation of Intestinal T Lymphocyte Development
CCR6 对肠道 T 淋巴细胞发育的调节
- 批准号:
7035400 - 财政年份:2004
- 资助金额:
$ 0.4万 - 项目类别:
CCR6 Regulation of Intestinal T Lymphocyte Development
CCR6 对肠道 T 淋巴细胞发育的调节
- 批准号:
6775267 - 财政年份:2004
- 资助金额:
$ 0.4万 - 项目类别:
Regulation of Organized Intestinal Lymphoid Tissues by TRANCE/RANKL
TRANCE/RANKL 对有组织肠淋巴组织的调节
- 批准号:
7928053 - 财政年份:2004
- 资助金额:
$ 0.4万 - 项目类别:
Regulation of Organized Intestinal Lymphoid Tissues by TRANCE/RANKL
TRANCE/RANKL 对有组织肠淋巴组织的调节
- 批准号:
8432109 - 财政年份:2004
- 资助金额:
$ 0.4万 - 项目类别:
Regulation of Organized Intestinal Lymphoid Tissues by TRANCE/RANKL
TRANCE/RANKL 对有组织肠淋巴组织的调节
- 批准号:
8325162 - 财政年份:2004
- 资助金额:
$ 0.4万 - 项目类别:
相似国自然基金
Neo-antigens暴露对肾移植术后体液性排斥反应的影响及其机制研究
- 批准号:2022J011295
- 批准年份:2022
- 资助金额:10.0 万元
- 项目类别:省市级项目
结核分枝杆菌持续感染期抗原(latency antigens)的重组BCG疫苗研究
- 批准号:30801055
- 批准年份:2008
- 资助金额:19.0 万元
- 项目类别:青年科学基金项目
相似海外基金
Bovine herpesvirus 4 as a vaccine platform for African swine fever virus antigens in pigs
牛疱疹病毒 4 作为猪非洲猪瘟病毒抗原的疫苗平台
- 批准号:
BB/Y006224/1 - 财政年份:2024
- 资助金额:
$ 0.4万 - 项目类别:
Research Grant
A novel vaccine approach combining mosquito salivary antigens and viral antigens to protect against Zika, chikungunya and other arboviral infections.
一种结合蚊子唾液抗原和病毒抗原的新型疫苗方法,可预防寨卡病毒、基孔肯雅热和其他虫媒病毒感染。
- 批准号:
10083718 - 财政年份:2023
- 资助金额:
$ 0.4万 - 项目类别:
Small Business Research Initiative
Uncovering tumor specific antigens and vulnerabilities in ETP-acute lymphoblastic leukemia
揭示 ETP-急性淋巴细胞白血病的肿瘤特异性抗原和脆弱性
- 批准号:
480030 - 财政年份:2023
- 资助金额:
$ 0.4万 - 项目类别:
Operating Grants
Regulation of B cell responses to vaccines by long-term retention of antigens in germinal centres
通过在生发中心长期保留抗原来调节 B 细胞对疫苗的反应
- 批准号:
MR/X009254/1 - 财政年份:2023
- 资助金额:
$ 0.4万 - 项目类别:
Research Grant
Adaptive Discrimination of Risk of Antigens in Immune Memory Dynamics
免疫记忆动态中抗原风险的适应性辨别
- 批准号:
22KJ1758 - 财政年份:2023
- 资助金额:
$ 0.4万 - 项目类别:
Grant-in-Aid for JSPS Fellows
22-ICRAD Call 2 - Improving the diagnosis of tuberculosis in domestic ruminants through the use of new antigens and test platforms
22-ICRAD 呼吁 2 - 通过使用新抗原和测试平台改善家养反刍动物结核病的诊断
- 批准号:
BB/Y000927/1 - 财政年份:2023
- 资助金额:
$ 0.4万 - 项目类别:
Research Grant
Protective immunity elicited by distinct polysaccharide antigens of classical and hypervirulent Klebsiella
经典和高毒力克雷伯氏菌的不同多糖抗原引发的保护性免疫
- 批准号:
10795212 - 财政年份:2023
- 资助金额:
$ 0.4万 - 项目类别:
Integrative proteome analysis to harness humoral immune response against tumor antigens
综合蛋白质组分析利用针对肿瘤抗原的体液免疫反应
- 批准号:
23K18249 - 财政年份:2023
- 资助金额:
$ 0.4万 - 项目类别:
Grant-in-Aid for Challenging Research (Exploratory)
Targeting T3SA proteins as protective antigens against Yersinia
将 T3SA 蛋白作为针对耶尔森氏菌的保护性抗原
- 批准号:
10645989 - 财政年份:2023
- 资助金额:
$ 0.4万 - 项目类别:
Functionally distinct human CD4 T cell responses to novel evolutionarily selected M. tuberculosis antigens
功能独特的人类 CD4 T 细胞对新型进化选择的结核分枝杆菌抗原的反应
- 批准号:
10735075 - 财政年份:2023
- 资助金额:
$ 0.4万 - 项目类别: