EAGER: Biomanufacturing: Towards Reproducible and Scalable Biomanufacturing of Tumor-Specific T Cells with Optimal Phenotype and Function for Personalized Immunotherapy
EAGER: Biomanufacturing: Towards Reproducible and Scalable Biomanufacturing of Tumor-Specific T Cells with Optimal Phenotype and Function for Personalized Immunotherapy
批准号:
1645229
负责人:
Fei Wen
金额:
$30.0万
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-09-01 至 2019-08-31
中文摘要
1645229-温氏癌症导致了美国约25%的死亡。开发一种有效的过继T细胞疗法(ACT),是一种有前途的高度个性化的癌症免疫疗法,具有显著的社会效益。然而,开发可重复和可扩展的制造工艺以可靠地产生具有高抗肿瘤活性的T细胞仍然是一个重大挑战。该项目旨在通过开发一种快速、简单和全面的T细胞特征分析方法来应对这一挑战。它代表了一种全新的、具有变革潜力的方法,通过解决ACT商业化的多个障碍,包括制造重复性、治疗有效性和患者之间的差异性。研究成果还将用于加强本科生和研究生课程,推动工程推广努力,鼓励K-12学生及早接触科学和工程,并提高公众的科学素养。将开发创新的教学方法,各级教育工作者可以很容易地结合起来,以改善他们的学生的学习。这些努力将共同帮助培养具有工程和生命科学方面的技能和基础知识的新一代工程师。过继T细胞疗法(ACT)是一种高度个性化的癌症免疫疗法,涉及将体外制造的天然或基因工程肿瘤反应性T细胞注入患者体内。单个幼稚的人类T细胞的扩增产生了一个表现出一系列表型和功能的异质群体。虽然这种多样性有助于T细胞在不同阶段对不同类型的病原体和癌症产生专门的反应,但这对可重复、大规模生产用于治疗目的的T细胞来说是一个重大的技术挑战。因此,拥有一种高性能的T细胞图谱方法来密切监测其表型、功能和特异性是至关重要的。不幸的是,目前的标准技术需要几个样本运行,增加了制造过程的复杂性、可变性和工作量。为了解决这个问题,将开发一种T细胞特征分析方法,以便能够在一次运行中同时检测异质群体中单个T细胞的数十个参数。将开发所产生的高维数据的可视化方法,以促进制造过程质量控制步骤中的客观数据分析自动化。同时,通过开发和应用一种创新的人工抗原呈递系统,乳腺癌中发现的一系列次要肿瘤相关抗原的特异性T细胞将从人类捐赠者那里扩大。与这里开发的T细胞图谱方法相结合,这些T细胞提供了宝贵的机会来系统地筛选亚优势T细胞的最佳扩增条件,并确定它们与最佳抗肿瘤活性相关的分子指标。这些指标的定义将进一步简化质量控制协议,并促进ACT制造过程的标准化。
英文摘要
1645229 - Wen Cancer is responsible for about 25% of deaths in the US. Developing an effective adoptive T-cell therapy (ACT), a promising and highly personalized cancer immunotherapy, holds significant benefits for society. However, it remains a significant challenge to develop reproducible and scalable manufacturing processes to reliably generate T cells with high anti-tumor activity. This project aims to address this challenge by developing a rapid, simple, and comprehensive T-cell profiling method. It represents a novel and radically different approach with transformative potential by addressing multiple roadblocks to the commercialization of ACT, including manufacturing reproducibility, therapeutic effectiveness and patient-to-patient variability. Research findings will also be used to strengthen undergraduate and graduate curricula, to power engineering outreach endeavors that encourage early exposure of K-12 students to science and engineering, and to increase public scientific literacy. Innovative pedagogies will be developed that can be readily incorporated by educators at all levels to improve their students' learning. These efforts will collectively help create a new generation of engineers with skills and fundamental knowledge in both engineering and life sciences. Adoptive T-cell therapy (ACT) is a highly personalized cancer immunotherapy that involves the infusion into patients of their natural or genetically engineered tumor-reactive T cells manufactured ex vivo. Expansion of a single naïve human T cell yields a heterogeneous population exhibiting a range of phenotype and function. While this diversity helps T cells acquire specialized responses to different types of pathogens and cancers at different stages, it represents a significant technical challenge to reproducible, large-scale manufacturing of T cells for therapeutic purposes. Therefore, it is critical to have a high performance T-cell profiling method to closely monitor their phenotype, function and specificity. Unfortunately, the current standard technology requires several sample runs, adding complexity, variability and workload to the manufacturing process. To address this issue, a T-cell profiling method will be developed to enable simultaneous detection of dozens of parameters on single T cells in a heterogeneous population in a single run. Visualization methods of the resulting high-dimensional data will be developed to facilitate objective data-analysis automation in the quality control steps of the manufacturing process. In parallel, by developing and applying an innovative artificial antigen presentation system, T cells specific to a range of subdominant tumor-associated antigens found in breast cancer will be expanded from human donors. Coupled with the T-cell profiling method developed here, these T cells provide valuable opportunities to systematically screen for optimal expansion conditions of subdominant T cells and define their molecular metrics that correlate with the best anti-tumor activity. The definition of such metrics will further simplify the quality control protocol and facilitate the standardization of the ACT manufacturing process.
期刊论文(6)
专著(0)
科研奖励(0)
会议论文
Rapid microsphere‐assisted peptide screening (MAPS) of promiscuous MHCII‐binding peptides in Zika virus envelope protein
寨卡病毒包膜蛋白中混杂的 MHCII 结合肽的快速微球辅助肽筛选 (MAPS)
DOI:
10.1002/aic.16697
发表时间:
2019
期刊:
AIChE Journal
影响因子:
3.7
作者:
[Smith, Mason R., Bugada, Luke F., Wen, Fei]
通讯作者:
Wen, Fei
DOI:
10.1172/jci.insight.127291
发表时间:
2019-04-18
期刊:
JCI INSIGHT
影响因子:
8
作者:
[Billi, Allison C., Gharaee-Kermani, Mehrnaz, Gudjonsson, Johann E.]
通讯作者:
Gudjonsson, Johann E.
DOI:
10.1021/acscatal.8b01883
发表时间:
2018-09-01
期刊:
ACS CATALYSIS
影响因子:
12.9
作者:
[Bugada, Luke F., Smith, Mason R., Wen, Fei]
通讯作者:
Wen, Fei
CAREER: An ImmunoBioEngineering Platform for Rapid and Scalable Biomanufacturing of Universal Viral Vaccines
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批准号:1653611
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项目类别:Standard Grant
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资助金额:$50.0万
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财政年份:2017
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负责人:Fei Wen
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依托单位:
UNS: Tunable and Scalable Protein Assemblies for Personalized Cancer Immunotherapy
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批准号:1511720
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项目类别:Standard Grant
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资助金额:$34.0万
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财政年份:2015
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负责人:Fei Wen
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依托单位:
海外基金