Training in the Molecular Basis of Autoimmunity and Autoinflammation
自身免疫和自身炎症的分子基础培训
基本信息
- 批准号:10442502
- 负责人:
- 金额:$ 14.69万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2018
- 资助国家:美国
- 起止时间:2018-09-01 至 2023-08-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
ABSTRACT
The past 15 years has seen a paradigm shift in our understanding of the complex mechanisms underlying
autoimmune diseases with a greater understanding of the interplay between innate and adaptive immune
system components, the mechanisms that lead to innate and adaptive immune mediated tissue destruction,
the relevance of animal models to human disease, and the factors needed to generate functional transplant
tissue. To capitalize on all of these insights and develop novel therapeutic strategies that block autoreactive
responses and also permit the repair and/or replacement of damaged organs, will require a next generation of
scientists with a broad understanding of basic immunology, cell biology, molecular biology, systems biology
and informatics. The proposed Training in the Molecular Basis of Autoimmunity and Autoinflammation will train
predoctoral investigators in these important areas by bringing together highly skilled and collaborative mentors
from multiple disciplines, with the ultimate goal of developing new therapies for these debilitating diseases. We
have also learned that an array of susceptibility genes are shared among autoimmune diseases, indicative of
common pathways. A better understanding of how these susceptibility genes promote the loss of tolerance and
hyperreactivity will also be key to effective treatments for autoimmune diseases. To train investigators to meet
these challenges of scientific inquiry, our training environments must embrace cross-disciplinary themes and
provide both state-of-the-art research opportunities in this area, and also provide training in other aspects of
career development. Therefore, the specific goals of this program will be to: (1) provide talented PhD
candidates with conceptual and technological skills to tackle meaningful, clinically relevant topics in the area of
autoimmunity; (2) facilitate communication and collaborative interactions amongst trainees and training faculty;
(3) provide opportunities for the translation of research discoveries to the clinics; (4) establish mechanisms for
recruiting increased numbers underrepresented minorities to postdoctoral positions at this institution; (5)
provide trainees with strong oral presentation, manuscript writing, grant writing, networking, and other essential
career development skills; and (6) provide trainees with opportunities to participate in local, national, and
international meetings where they can share their own research findings. The program is highly cross-
disciplinary, incorporating 18 accomplished investigators as mentors who represent a broad spectrum of
research expertise and technologies that are being applied to the study of autoimmune/autoinflammatory
conditions. The training faculty includes MD and MD-PhD scientists engaged in basic and translational,
disease-oriented research. Faculty members are already involved in highly productive collaborations and have
extensive experience in predoctoral training. The program co-directors will be advised by both the training
faculty and an External Advisory Committee comprised of distinguished scientists/training grant directors with
interests in autoimmunity and autoinflammation. Importantly, the program directors will work closely with the
UMMS Office of Career Development to provide training in critical career skills that will further enable trainees
to carry their research accomplishments forward to successful academic careers.
抽象的
过去 15 年,我们对复杂机制的理解发生了范式转变
自身免疫性疾病,更好地了解先天免疫和适应性免疫之间的相互作用
系统组成部分,导致先天性和适应性免疫介导的组织破坏的机制,
动物模型与人类疾病的相关性,以及产生功能性移植所需的因素
组织。利用所有这些见解并开发阻止自身反应的新治疗策略
响应并允许修复和/或更换受损器官,将需要下一代
对基础免疫学、细胞生物学、分子生物学、系统生物学有广泛了解的科学家
和信息学。拟议的自身免疫和自身炎症分子基础培训将培训
通过汇集高技能且协作的导师,在这些重要领域培养博士前研究人员
来自多个学科,最终目标是为这些使人衰弱的疾病开发新疗法。我们
还了解到,自身免疫性疾病有一系列的易感基因,这表明
共同途径。更好地了解这些易感基因如何促进耐受性的丧失和
过度反应也将是有效治疗自身免疫性疾病的关键。培训调查人员会面
这些科学探究的挑战,我们的培训环境必须涵盖跨学科主题和
提供该领域最先进的研究机会,并提供其他方面的培训
职业发展。因此,该项目的具体目标是:(1)培养博士人才
具有概念和技术技能的候选人,可以解决该领域有意义的、临床相关的主题
自身免疫; (2) 促进学员和培训教师之间的沟通和协作互动;
(3) 提供将研究发现转化为临床的机会; (四)建立机制
招募更多数量不足的少数族裔担任该机构的博士后职位; (5)
为学员提供强有力的口头表达、手稿写作、资助写作、网络和其他必要的能力
职业发展技能; (6) 为学员提供参加地方、国家和地区的机会
他们可以在国际会议上分享自己的研究成果。该计划具有高度交叉性
学科,吸收了 18 名卓有成效的研究者作为导师,他们代表了广泛的领域
应用于自身免疫/自身炎症研究的研究专业知识和技术
状况。培训师资包括从事基础和转化、
以疾病为导向的研究。教职员工已经参与了高效的合作,并且已经
丰富的博士前培训经验。培训双方都将向项目联合主任提供建议
教师和外部咨询委员会由杰出科学家/培训资助主任组成
对自身免疫和自身炎症感兴趣。重要的是,项目主管将与
UMMS 职业发展办公室将提供关键职业技能培训,进一步帮助受训者
将他们的研究成果推进到成功的学术生涯。
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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Katherine A. Fitzgerald其他文献
Genetic Models Reveal cis and trans Immune-Regulatory Activities for lincRNA-Cox2
遗传模型揭示 lincRNA-Cox2 的顺式和反式免疫调节活性
- DOI:
10.3390/epigenomes3030014 - 发表时间:
2024-09-13 - 期刊:
- 影响因子:2.5
- 作者:
Rol;Elling;E. K. Robinson;Barbara Shapleigh;Stephen C. Liapis;S. Covarrubias;Sol Katzman;A. Groff;Zhaozhao Jiang;S. Agarwal;M. Motwani;Jennie Chan;Shrutie Sharma;Elizabeth J Hennessy;Garret A. FitzGerald;Michael T. McManus;J. Rinn;Katherine A. Fitzgerald;Susan B. Carpenter - 通讯作者:
Susan B. Carpenter
STING channels its proton power.
STING 引导其质子能量。
- DOI:
10.1016/j.molcel.2023.09.014 - 发表时间:
2023-10-01 - 期刊:
- 影响因子:16
- 作者:
Mingqi Dong;Katherine A. Fitzgerald - 通讯作者:
Katherine A. Fitzgerald
Quantifying and Mitigating Motor Phenotypes Induced by Quantifying and Mitigating Motor Phenotypes Induced by Antisense Oligonucleotides in the Central Nervous System Antisense Oligonucleotides in the Central Nervous System
量化和减轻中枢神经系统中反义寡核苷酸诱导的运动表型 量化和减轻中枢神经系统中反义寡核苷酸诱导的运动表型
- DOI:
- 发表时间:
2022 - 期刊:
- 影响因子:0
- 作者:
Michael P. Moazami;Julia M. Rembetsy;Feng Wang;P. M. Krishnamurthy;Alexandra Weiss;M. Marosfoi;Robert M. King;M. Motwani;H. Gray;Katherine A. Fitzgerald;Robert H Brown;Jonathan K. Watts - 通讯作者:
Jonathan K. Watts
Lnc-ing RNA to intestinal homeostasis and inflammation.
Lnc-ing RNA 影响肠道稳态和炎症。
- DOI:
10.1016/j.it.2023.12.005 - 发表时间:
2024-01-01 - 期刊:
- 影响因子:16.8
- 作者:
Katherine A. Fitzgerald;Liraz Shmuel - 通讯作者:
Liraz Shmuel
Gene coexpression networks reveal a broad role for lncRNAs in inflammatory bowel disease
基因共表达网络揭示了lncRNA在炎症性肠病中的广泛作用
- DOI:
10.1172/jci.insight.168988 - 发表时间:
2024-02-08 - 期刊:
- 影响因子:8
- 作者:
John L Johnson;Davit Sargsyan;Eric M Neiman;Amy Hart;A. Stojmirović;Roman Kosoy;H. Irizar;M. Suárez;Won;Carmen Argmann;Stefan Avey;Liraz Shmuel;Tim Vierbuchen;Gerold Bongers;Yu Sun;Leonard Edelstein;J. Perrigoue;Jennifer E. Towne;Aisling O'Hara Hall;Katherine A. Fitzgerald;Kasper Hoebe - 通讯作者:
Kasper Hoebe
Katherine A. Fitzgerald的其他文献
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{{ truncateString('Katherine A. Fitzgerald', 18)}}的其他基金
Radioresistant Innate Immunity in SAVI Tissue-Specific Autoinflammation
SAVI 组织特异性自身炎症中的抗辐射先天免疫
- 批准号:
10752556 - 财政年份:2023
- 资助金额:
$ 14.69万 - 项目类别:
9th Annual meeting of the International Cytokine and Interferon Society Meeting
国际细胞因子和干扰素学会第九届年会
- 批准号:
10389980 - 财政年份:2021
- 资助金额:
$ 14.69万 - 项目类别:
Training in the Molecular Basis of Autoimmunity and Autoinflammation
自身免疫和自身炎症的分子基础培训
- 批准号:
10712784 - 财政年份:2018
- 资助金额:
$ 14.69万 - 项目类别:
Training in the Molecular Basis of Autoimmunity and Autoinflammation
自身免疫和自身炎症的分子基础培训
- 批准号:
10201428 - 财政年份:2018
- 资助金额:
$ 14.69万 - 项目类别:
Regulation of Lupus by Cytosolic DNA Sensors
细胞质 DNA 传感器对狼疮的调节
- 批准号:
9229764 - 财政年份:2017
- 资助金额:
$ 14.69万 - 项目类别:
Characterization of Chromatin associated Long non-coding in immunity
免疫中染色质相关长非编码的表征
- 批准号:
8809301 - 财政年份:2014
- 资助金额:
$ 14.69万 - 项目类别:
Characterization of Chromatin associated Long non-coding in immunity
免疫中染色质相关长非编码的表征
- 批准号:
8966645 - 财政年份:2014
- 资助金额:
$ 14.69万 - 项目类别:
DNA sensors and associated signaling pathways in the innate immune response
先天免疫反应中的 DNA 传感器和相关信号通路
- 批准号:
8297717 - 财政年份:2012
- 资助金额:
$ 14.69万 - 项目类别:
DNA sensors and associated signaling pathways in the innate immune response
先天免疫反应中的 DNA 传感器和相关信号通路
- 批准号:
8606390 - 财政年份:2012
- 资助金额:
$ 14.69万 - 项目类别:
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