UCSF Center for Synthetic Immunology: Tools to Reprogram the Immune System to Combat Cancer
加州大学旧金山分校合成免疫学中心:重新编程免疫系统以对抗癌症的工具
基本信息
- 批准号:10598367
- 负责人:
- 金额:$ 5.93万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2019
- 资助国家:美国
- 起止时间:2019-09-24 至 2024-08-31
- 项目状态:已结题
- 来源:
- 关键词:AddressAntigensBioinformaticsCell TherapyCellsCellular immunotherapyDatabasesEngineeringGene Expression ProfilingGoalsHematopoietic NeoplasmsImmuneImmune systemImmunologistImmunotherapeutic agentMalignant NeoplasmsModelingNormal tissue morphologyPattern RecognitionProcessSafetyScientistSolidSolid NeoplasmSynthetic immunologyTechnologyblood treatmentcell behaviorcell transformationcellular engineeringchimeric antigen receptor T cellscombatcomputer frameworkdesignengineered T cellsimmunoengineeringin vivonanonanomaterialsneoplastic cellnext generationprogramsprototypesmall moleculetooltraffickingtumortumor microenvironment
项目摘要
Project Summary/Abstract
UCSF Center for Synthetic Immunology: Tools to Reprogram the Immune System to Combat Cancer
The immune system has emerged as an extraordinarily powerful tool for combating cancer. One of the most
potent agents are engineered T cells programmed to recognize and kill tumor cells. Nonetheless, our ability to
engineer T cells and other immune cells and program them to execute new functions remains relatively primitive.
Aside from CAR T cells for treatment of blood cancers, most engineered cell therapies are risky, potentially highly
toxic, unreliable and often ineffective, especially those cell therapies that attempt to target solid cancers. We
hypothesize that to fulfil the promise of engineered immune cell therapies, we must first transform cell
engineering into a systematic and predictable process; one that uses reliable technology platforms and
principles. Our center will focus on developing a set of sophisticated immune engineering platforms that address
three major needs in next-generation cell therapies:
1) Smart recognition of cancer – develop antigen-pattern recognition circuits that direct immune cells to
optimally recognize solid tumors and discriminate against normal tissue crossreaction, guided by
computational bioinformatic analysis of gene expression patterns.
2) Overcoming the tumor microenvironment – develop multiple classes of cellular circuits that can overcome
or locally remodel immune-suppressive tumor microenvironments to promote highly efficient therapeutic
immune cell trafficking, proliferation, persistence, and tumor-killing activity
3) User-control and safety – to increase control over and safety of these powerful engineered cells, we will
develop a suite of ways to communicate with and control the activity of engineered immune cells in vivo,
including nano/microparticles and small molecules.
To achieve these goals, we have assembled the UCSF Center for Synthetic Immunology, a tightly integrated
interdisciplinary team that encompasses synthetic biologists, immunologists, bio-informaticists, control
engineers, and materials scientists. The products of this center will include publicly available toolkits of parts
and circuits for cell engineering, high-throughput platforms for rapid circuit assembly, new programmable
nanomaterials for controlling immune cell behavior, searchable bioinformatic databases for optimization of tumor
recognition, and computational frameworks for circuit design and for modeling/prototyping in vivo circuit function.
These platforms will help to advance immune cell engineering to be far more reliable, predictable, effective and
safe.
项目总结/文摘
项目成果
期刊论文数量(8)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Discriminatory Power of Combinatorial Antigen Recognition in Cancer T Cell Therapies.
- DOI:10.1016/j.cels.2020.08.002
- 发表时间:2020-09-23
- 期刊:
- 影响因子:9.3
- 作者:Dannenfelser R;Allen GM;VanderSluis B;Koegel AK;Levinson S;Stark SR;Yao V;Tadych A;Troyanskaya OG;Lim WA
- 通讯作者:Lim WA
Golden age of immunoengineering.
免疫工程的黄金时代。
- DOI:10.1111/imr.13283
- 发表时间:2023
- 期刊:
- 影响因子:8.7
- 作者:Wong,WilsonW;Lim,WendellA
- 通讯作者:Lim,WendellA
Engineering cytokines and cytokine circuits.
- DOI:10.1126/science.abb5607
- 发表时间:2020-11-27
- 期刊:
- 影响因子:0
- 作者:Li AW;Lim WA
- 通讯作者:Lim WA
T cell circuits that sense antigen density with an ultrasensitive threshold.
- DOI:10.1126/science.abc1855
- 发表时间:2021-03-12
- 期刊:
- 影响因子:0
- 作者:Hernandez-Lopez RA;Yu W;Cabral KA;Creasey OA;Lopez Pazmino MDP;Tonai Y;De Guzman A;Mäkelä A;Saksela K;Gartner ZJ;Lim WA
- 通讯作者:Lim WA
The emerging era of cell engineering: Harnessing the modularity of cells to program complex biological function.
细胞工程的新兴时代:利用细胞的模块化来编程复杂的生物功能。
- DOI:10.1126/science.add9665
- 发表时间:2022
- 期刊:
- 影响因子:0
- 作者:Lim,WendellA
- 通讯作者:Lim,WendellA
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WENDELL A LIM的其他文献
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{{ truncateString('WENDELL A LIM', 18)}}的其他基金
Engineering synthetic immune cells with modular sentinel and therapeutic functions for T1D
工程合成免疫细胞具有模块化前哨和 T1D 治疗功能
- 批准号:
10594512 - 财政年份:2022
- 资助金额:
$ 5.93万 - 项目类别:
Ameliorating off-target toxicities of CAR T cells by engineering NOT gates
通过设计 NOT 门改善 CAR T 细胞的脱靶毒性
- 批准号:
10657356 - 财政年份:2022
- 资助金额:
$ 5.93万 - 项目类别:
Engineering synthetic immune cells with modular sentinel and therapeutic functions for T1D
工程合成免疫细胞具有模块化前哨和 T1D 治疗功能
- 批准号:
10436126 - 财政年份:2022
- 资助金额:
$ 5.93万 - 项目类别:
Ameliorating off-target toxicities of CAR T cells by engineering NOT gates
通过设计 NOT 门改善 CAR T 细胞的脱靶毒性
- 批准号:
10362126 - 财政年份:2022
- 资助金额:
$ 5.93万 - 项目类别:
Recognizing the tumor ecosystem: Integrating stromal and cancer antigen signals to achieve precision recognition of solid tumors by CAR T cells
识别肿瘤生态系统:整合基质信号和癌抗原信号,实现CAR T细胞对实体瘤的精准识别
- 批准号:
10094815 - 财政年份:2020
- 资助金额:
$ 5.93万 - 项目类别:
Recognizing the tumor ecosystem: Integrating stromal and cancer antigen signals to achieve precision recognition of solid tumors by CAR T cells
识别肿瘤生态系统:整合基质信号和癌抗原信号,实现CAR T细胞对实体瘤的精准识别
- 批准号:
10559489 - 财政年份:2020
- 资助金额:
$ 5.93万 - 项目类别:
Recognizing the tumor ecosystem: Integrating stromal and cancer antigen signals to achieve precision recognition of solid tumors by CAR T cells
识别肿瘤生态系统:整合基质信号和癌抗原信号,实现CAR T细胞对实体瘤的精准识别
- 批准号:
10310406 - 财政年份:2020
- 资助金额:
$ 5.93万 - 项目类别:
Engineering synthetic helper cells that autonomously deliver orthogonal IL-2 to selectively promote therapeutic T cell proliferation in tumors
工程合成辅助细胞可自主递送正交 IL-2 以选择性促进肿瘤中治疗性 T 细胞增殖
- 批准号:
10285941 - 财政年份:2019
- 资助金额:
$ 5.93万 - 项目类别:
UCSF Center for Synthetic Immunology: Tools to Reprogram the Immune System to Combat Cancer
加州大学旧金山分校合成免疫学中心:重新编程免疫系统以对抗癌症的工具
- 批准号:
10598362 - 财政年份:2019
- 资助金额:
$ 5.93万 - 项目类别:
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