Customized stem cells for clinical application in blood disorders

定制干细胞用于血液疾病的临床应用

基本信息

批准号：
8541537
负责人：
JAMES J COLLINS
金额：
$ 0.78万
依托单位：
BOSTON CHILDREN'S HOSPITAL
依托单位国家：
美国
项目类别：
财政年份：
2011
资助国家：
美国
起止时间：
2011-09-19 至 2014-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8541537
关键词：
Address Autologous Biological Biomechanics Biomedical Engineering Bone Marrow Cell Transplants Cell model Cells Chemicals Clinical Clinical Trials Collaborations Computational algorithm Data Derivation procedure Development Disease Disease model Embryo Failure Gene Expression Genetic Genotype Goals Hematological Disease Hematopoietic Hematopoietic Stem Cell Transplantation Hematopoietic stem cells Hemoglobinopathies Home environment Human Immune Immunologics In Vitro Infection Intravenous infusion procedures Knowledge Lymphoid Malignant - descriptor Marrow Minority Mission Modeling Monoclonal Antibody R24 Mus Pathway interactions Patients Phenotype Pluripotent Stem Cells Population Preclinical Drug Evaluation Principal Investigator Production Protocols documentation Research Stem cell transplant Stem cells Testing Therapeutic Therapeutic Studies Transgenes Transplantation Zebrafish adverse outcome clinical application clinically relevant drug development gene correction gene discovery gene repair graft vs host disease induced pluripotent stem cell insight leukemia loss of function morphogens mortality novel progenitor stem stem cell population success transcription factor

项目摘要

DESCRIPTION (provided by applicant): This proposal brings together an interdisciplinary team of collaborators to address a major challenge: to achieve clinical utility of patient-specific induced pluripotent stem cells (iPSCs) for blood diseases. Our ultimate goal is to differentiate customized iPSCs into hematopoietic stem and progenitor cells to accurately model human blood diseases for research into disease mechanisms, and as a platform for treating patients with blood diseases. To achieve this, this proposal aims to discover the developmental pathways and biomechanical principles that drive the formation of hematopoietic stem cells (HSCs) in embryos, and will screen for morphogens and chemicals that promote hematopoietic maturation in vitro. We will take several novel and integrated approaches including: 1) application of predictive computational algorithms to gene expression data from highly purified embryonic HSC populations to discover the gene networks that direct hematopoietic and lymphoid development; 2) Screens in zebrafish embryos and murine and human pluripotent stem cells to discover novel chemical and biological regulators of HSCs; 3) bioengineered platforms for production of hematopoietic stem and progenitor populations, applying biomechanical forces to mimic the embryonic microenvironment; 4) derivation of iPSC from patients with Primary Immune Deficiency to correlate genotype with lymphoid phenotypes and to test strategies for gene repair through an "in vitro clinical trial"; and ultimately, 5) to derive transgene-free clinical-grade pluripotent stem cells, and develop protocols for differentiation of hematopoietic populations at clinical scale. Success in generating engraftable, genetically unperturbed HSC would be a significant breakthrough that would enhance the utility of iPSC for modeling hematopoietic disease and establish a translational platform for combining gene repair with HSC transplantation therapy.

描述（由申请人提供）：该提案汇集了一个跨学科的合作团队来解决一项重大挑战：实现患者特异性诱导多能干细胞（iPSC）在血液疾病中的临床应用。我们的最终目标是将定制的iPSC分化为造血干细胞和祖细胞，以准确地模拟人类血液疾病，以研究疾病机制，并作为治疗血液疾病患者的平台。为了实现这一目标，该提案旨在发现驱动胚胎中造血干细胞（HSC）形成的发育途径和生物力学原理，并将筛选促进体外造血成熟的形态发生素和化学物质。我们将采取几种新颖的综合方法，包括：1）将预测计算算法应用于来自高度纯化的胚胎HSC群体的基因表达数据，以发现指导造血和淋巴发育的基因网络； 2) 筛选斑马鱼胚胎以及小鼠和人类多能干细胞，发现 HSC 的新型化学和生物调节因子； 3）用于生产造血干细胞和祖细胞群的生物工程平台，应用生物力学来模拟胚胎微环境； 4) 从原发性免疫缺陷患者中提取 iPSC，将基因型与淋巴表型相关联，并通过“体外临床试验”测试基因修复策略；最终，5) 获得无转基因的临床级多能干细胞，并开发临床规模的造血群体分化方案。成功生成可移植、遗传不受干扰的 HSC 将是一项重大突破，将增强 iPSC 在造血疾病建模中的效用，并建立一个将基因修复与 HSC 移植治疗相结合的转化平台。