Resource for Molecular Imaging Agents in Precision Medicine
精准医学分子成像剂资源
基本信息
- 批准号:10226206
- 负责人:
- 金额:$ 117.95万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2017
- 资助国家:美国
- 起止时间:2017-09-15 至 2024-06-30
- 项目状态:已结题
- 来源:
- 关键词:AddressAutologous TransplantationBiologicalBiological MarkersBiomedical TechnologyBrain imagingCAR T cell therapyCancer VaccinesCaringCell LineCell TransplantationCell surfaceCellsChemical AgentsChemicalsChemistryClinicClinicalCollaborationsCommunitiesDataDetectionDevelopmentDiscipline of Nuclear MedicineEducationEnvironmentFOLH1 geneGenerationsGeneticGenetically Engineered MouseGoalsGrantHandHistopathologyHumanImageImmersionImmunityImmunohistochemistryImmunooncologyImmunotherapyIndustryInflammationInflammatoryInfrastructureInstitutesInvestmentsJournalsLibrariesLinkLocationMalignant NeoplasmsMedicalMethodsMissionMolecular GeneticsNational Institute of Biomedical Imaging and BioengineeringNew AgentsOrganic SynthesisPatient CarePatientsPeptidesPeptoidsPharmacologyPhenotypePositron-Emission TomographyPreclinical TestingProcessRadiology SpecialtyReagentRecording of previous eventsReporterResearchResourcesSchoolsServicesSiteSystemTechnical ExpertiseTechnologyTrainingTransgenic OrganismsTranslatingTranslationsUnited States National Institutes of HealthUniversitiesValidationWorkanticancer researcharmcancer cellcancer imagingcancer immunotherapycellular imagingcommercializationcostdesignflexibilityhandicapping conditionhuman imagingimaging agentimaging modalityimaging systemimmune checkpointin vitro Modelin vivoin vivo monitoringinstrumentationlecturesmolecular imagingneuroinflammationnext generationnuclear divisionphase II trialpre-clinicalprecision medicineprogramsradioligandradiotracerresearch and developmentside effectsmall moleculetargeted agenttechnology developmenttheranosticstumortumor microenvironmentweb site
项目摘要
OVERALL RESOURCE: Summary
The Resource for Molecular Imaging Agents in Precision Medicine is a program spanning three campuses of the
Johns Hopkins University (JHU). In our view precision medicine is using all data at hand regarding a particular
patient to enable the best possible care for that patient. We believe that carefully designed molecular imaging
agents can contribute to this. We are now poised to offer a unique Biomedical Technology Resource Center
(BTRC) with a heavy emphasis on the provision of chemistry – new reagents, methods and training in their
development and practice – for molecular imaging. The biological theme of the BTRC is relationships between
cancer, inflammation and immunity, deeper study of which is an unmet need. Although brilliant research
continues worldwide in the development of new molecular imaging agents, few have had actual impact on
addressing human infirmity and many do not justify the cost of their development. In March 2014 the NIBIB
conducted a study “to better understand the reasons why more molecular imaging agents and instrumentation
developed with NIH grant support are not being translated to the clinic nor subsequently commercialized.” To
address those shortcomings, the JHU BTRC will be highly translational by leveraging the Center for Translational
Molecular Imaging (CTMI) at the Johns Hopkins Bayview medical campus, the F. M. Kirby Center for Functional
Brain Imaging at the Kennedy Krieger Institute, the Division of Cancer Imaging Research, and the Division of
Nuclear Medicine and Molecular Imaging, all of which are highly integrated into numerous departments and
schools at JHU. We have generated agents that have been licensed and are in the process of commercialization.
However to date those activities have been performed on an ad hoc basis, and we intend to expand upon them
in two new ways: (1) provide targeted and unique technical research and development (TR&D) projects that will
(2) enable widespread dissemination and training in their use, enhancing the capacity of the centers and divisions
noted above to perform their intended functions – discovery with intent to educate, promote new collaborative,
transdisciplinary research and to manage a variety of conditions, while addressing unanticipated effects of
emerging cancer immunotherapies. The unique aspect of the BTRC is its focus on provision of new, precision
materials, to test these pre-clinically and progress them to human use, delivered on-site or to our collaborators
in a format suitable for their implementation. We will assure proper off-site utilization through continual, reciprocal
education and “push-pull” interactions. The program is agnostic to imaging modality and composition of the
materials to provide, relying upon the specific expertise within each TR&D. In addition to sharing the goal of
leveraging chemistry for imaging, the four TR&Ds will be linked through the aforementioned biological theme.
They can briefly be summarized as focusing on new theranostics (TR&D 1), molecular-genetic imaging systems
(TR&D 2), agents for probing immunity (TR&D 3), and targeted agents for chemical exchange saturation transfer
(CEST, TR&D 4). Within TR&Ds 1 and 3 are also the Pre-clinical and Clinical Validation cores, respectively.
总体资源:摘要
精密医学中分子成像剂的资源是一个跨越三个校园的程序
约翰·霍普金斯大学(JHU)。在我们看来,精确医学正在使用有关特定的所有数据
患者可以为该患者提供最佳护理。我们相信精心设计的分子成像
代理商可以为此做出贡献。现在,我们被毒品提供了一个独特的生物医学技术资源中心
(BTRC)强调化学的提供 - 新试剂,方法和培训
开发和实践 - 用于分子成像。 BTRC的生物学主题是
癌症,炎症和免疫力,更深入的研究是未满足的需求。虽然很棒的研究
在全球范围内,在新分子成像剂的发展中,很少有人对
解决人类患病的问题,许多人不能证明其发展的成本是合理的。 2014年3月尼比布
进行了一项研究“以更好地理解更多分子成像剂和仪器的原因
以NIH的赠款支持开发,没有被转化为诊所,也不会被商业化。”
解决这些缺点,JHU BTRC将通过利用翻译中心来高度翻译
Johns Hopkins Bayview Medical Campus的分子成像(CTMI),F。M。Kirby功能中心
肯尼迪·克里格研究所(Kennedy Krieger Institute)的脑成像,癌症成像研究部和
核医学和分子成像,所有这些都高度整合到众多部门中
Jhu的学校。我们已经生成了已获得许可并正在商业化过程中的代理商。
但是,迄今为止,这些活动已临时进行,我们打算扩大它们
通过两种新的方式:(1)提供针对性的独特技术研发(TR&D)项目
(2)在其使用中启用宽度传播和培训,增强了中心和部门的能力
上面注意到的是执行其预期功能 - 意图进行教育,促进新的合作活动,
跨学科研究并管理各种条件,同时解决了
新兴的癌症免疫疗法。 BTRC的独特方面是其专注于提供新的精确度
材料,预先链接地测试这些并将其推向人类使用,现场交付或我们的合作者
以适合其实施的格式。我们将通过连续的,倒数地假设适当的场外利用
教育和“推力”互动。该程序对成像方式和组成不可知
提供的材料,依靠每个TR&D中的特定专业知识。除了分享目标
利用化学成像,四个TR&D将通过近似生物学主题链接。
可以简要地总结为重点关注新的Theranostics(TR&D 1),分子遗传成像系统
(TR&D 2),探测免疫力的药物(TR&D 3),以及用于化学交换满意度转移的靶向代理
(Cest,TR&D 4)。在TR&D 1和3中,也分别是临床前和临床验证核心。
项目成果
期刊论文数量(46)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Acoustic-resolution photoacoustic microscope based on compact and low-cost delta configuration actuator.
- DOI:10.1016/j.ultras.2021.106549
- 发表时间:2022-01
- 期刊:
- 影响因子:4.2
- 作者:Gao S;Tsumura R;Vang DP;Bisland K;Xu K;Tsunoi Y;Zhang HK
- 通讯作者:Zhang HK
Carbon Dots as a New Class of Diamagnetic Chemical Exchange Saturation Transfer (diaCEST) MRI Contrast Agents.
- DOI:10.1002/anie.201904722
- 发表时间:2019-06
- 期刊:
- 影响因子:0
- 作者:Jia Zhang;Yue Yuan;Minling Gao;Zheng Han;Chengyan Chu;Yuguo Li;P. V. van Zijl;M. Ying;J. Bulte;Guanshu Liu
- 通讯作者:Jia Zhang;Yue Yuan;Minling Gao;Zheng Han;Chengyan Chu;Yuguo Li;P. V. van Zijl;M. Ying;J. Bulte;Guanshu Liu
6-O-(2-[18F]Fluoroethyl)-6-O-Desmethyl-Diprenorphine ([18F]FE-DPN) Preferentially Binds to Mu Opioid Receptors In Vivo.
6-O-(2-[18F]氟乙基)-6-O-去甲基-二丙诺啡 ([18F]FE-DPN) 在体内优先与 Mu 阿片受体结合。
- DOI:10.1007/s11307-022-01767-5
- 发表时间:2023
- 期刊:
- 影响因子:3.1
- 作者:Levinstein,MarjorieR;Ventriglia,EmilyaN;Gomez,JuanL;Budinich,ReeceC;Marton,János;Henriksen,Gjermund;Holt,DanielP;Dannals,RobertF;Pomper,MartinG;ZarateJr,CarlosA;Bonaventura,Jordi;Michaelides,Michael
- 通讯作者:Michaelides,Michael
A Unique Core-Shell Structured, Glycol Chitosan-Based Nanoparticle Achieves Cancer-Selective Gene Delivery with Reduced Off-Target Effects.
- DOI:10.3390/pharmaceutics14020373
- 发表时间:2022-02-07
- 期刊:
- 影响因子:5.4
- 作者:Cheng B;Ahn HH;Nam H;Jiang Z;Gao FJ;Minn I;Pomper MG
- 通讯作者:Pomper MG
Non-Invasive imaging of extracellular vesicles: Quo vaditis in vivo?
- DOI:10.1002/jev2.12241
- 发表时间:2022-07
- 期刊:
- 影响因子:16
- 作者:Arifin, Dian R.;Witwer, Kenneth W.;Bulte, Jeff W. M.
- 通讯作者:Bulte, Jeff W. M.
{{
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 }}
MARTIN G POMPER其他文献
MARTIN G POMPER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('MARTIN G POMPER', 18)}}的其他基金
Translational imaging biomarkers of the tumor microenvironment in early prostate cancer
早期前列腺癌肿瘤微环境的转化成像生物标志物
- 批准号:
10698133 - 财政年份:2022
- 资助金额:
$ 117.95万 - 项目类别:
Translational imaging biomarkers of the tumor microenvironment in early prostate cancer
早期前列腺癌肿瘤微环境的转化成像生物标志物
- 批准号:
10518916 - 财政年份:2022
- 资助金额:
$ 117.95万 - 项目类别:
Administration - Resource for Molecular Imaging Agents in Precision Medicine
管理 - 精准医学中分子成像剂的资源
- 批准号:
10226207 - 财政年份:2017
- 资助金额:
$ 117.95万 - 项目类别:
Training/Dissemination - Resource for Molecular Imaging Agents in Precision Medicine
培训/传播 - 精准医学分子成像剂资源
- 批准号:
10226214 - 财政年份:2017
- 资助金额:
$ 117.95万 - 项目类别:
Imaging Agents for Inflammatory Components of Malignancy
恶性肿瘤炎症成分的显像剂
- 批准号:
10226210 - 财政年份:2017
- 资助金额:
$ 117.95万 - 项目类别:
Small Molecule PSMA-Targeted Alpha Therapy
小分子 PSMA 靶向阿尔法疗法
- 批准号:
10594010 - 财政年份:2014
- 资助金额:
$ 117.95万 - 项目类别:
Small Molecule PSMA-Targeted Alpha Therapy
小分子 PSMA 靶向阿尔法疗法
- 批准号:
10411890 - 财政年份:2014
- 资助金额:
$ 117.95万 - 项目类别:
Small Molecule PSMA-Targeted Alpha Therapy
小分子 PSMA 靶向阿尔法疗法
- 批准号:
10092113 - 财政年份:2014
- 资助金额:
$ 117.95万 - 项目类别:
相似国自然基金
基于异种来源细胞外基质的组织工程化关节软骨移植物表面负载自体细胞膜与白蛋白生物涂层以获得移植物体内免疫逃逸功能的机理研究
- 批准号:
- 批准年份:2019
- 资助金额:61 万元
- 项目类别:面上项目
基因修复的自体诱导多能干细胞来源的视网膜色素上皮细胞移植治疗视网膜色素变性的实验研究
- 批准号:81770970
- 批准年份:2017
- 资助金额:56.0 万元
- 项目类别:面上项目
小环DNA载体介导的自体内合成生物蛋白复合制剂对肾脏移植后免疫排斥反应治疗效果
- 批准号:81760293
- 批准年份:2017
- 资助金额:34.0 万元
- 项目类别:地区科学基金项目
应用动静脉短路和体内骨生物反应器技术自体异位构建带血管蒂的骨移植物及其对股骨头坏死的修复
- 批准号:81000809
- 批准年份:2010
- 资助金额:20.0 万元
- 项目类别:青年科学基金项目
自体成纤维母细胞移植治疗兔前交叉韧带损伤的生物力学研究
- 批准号:30870647
- 批准年份:2008
- 资助金额:33.0 万元
- 项目类别:面上项目
相似海外基金
Gene regulatory networks in early lung epithelial cell fate decisions
早期肺上皮细胞命运决定中的基因调控网络
- 批准号:
10587615 - 财政年份:2023
- 资助金额:
$ 117.95万 - 项目类别:
Targeting Dystroglycanopathies using Pluripotent-derived Myogenic Progenitors
使用多能源性肌源性祖细胞靶向肌营养不良症
- 批准号:
10561375 - 财政年份:2023
- 资助金额:
$ 117.95万 - 项目类别:
Deciphering unintended large gene modifications in gene editing for sickle cell disease
破译镰状细胞病基因编辑中意外的大基因修饰
- 批准号:
10720685 - 财政年份:2023
- 资助金额:
$ 117.95万 - 项目类别:
Improving in vitro preantral follicle development using novel bioengineered culture systems and pre-theca-like cells as a strategy for assisted reproduction
使用新型生物工程培养系统和卵泡膜前样细胞作为辅助生殖策略改善体外窦前卵泡发育
- 批准号:
10749434 - 财政年份:2023
- 资助金额:
$ 117.95万 - 项目类别:
Chemotherapy-free cure of hemoglobin disorders through base editing
通过碱基编辑无需化疗即可治愈血红蛋白疾病
- 批准号:
10754114 - 财政年份:2023
- 资助金额:
$ 117.95万 - 项目类别: