CLINICAL TRIAL: ADMINISTRATION OF PERIPHERAL BLOOD T-CELLS AND EBV SPECIFIC CTLS

临床试验：外周血 T 细胞和 EBV 特异性 CTLS 的施用

• 批准号: 8356663
• 负责人: CHRYSTAL U LOUIS
• 金额: $ 0.04万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-12-01 至 2011-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8356663
• 关键词: Autologous; Clinical Research; Clinical Trials; Dose; EBV-Specific Cytotoxic T-Lymphocyte; Funding; Grant; Monoclonal Antibodies; National Center for Research Resources; Neuroblastoma; PTPRC gene; Patients; Principal Investigator; Research; Research Infrastructure; Resources; Safety; Source; T-Lymphocyte; United States National Institutes of Health; cell type; cost; in vivo; peripheral blood; receptor; tumor

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. Objectives Primary Objective To evaluate the safety of escalating doses of 14g2a.zeta chimeric receptor transduced autologous EBV specific cytotoxic T-lymphocytes (EBV-CTL) and 14g2a.zeta transduced autologous peripheral blood T-cells administered to patients with Neuroblastoma who have been lymphodepleted by CD45 monoclonal antibodies (MAbs). Secondary Objectives To determine the differential survival and function of these two infused cell-types in vivo, in particular to determine if chimeric receptor transduced EBV-CTLs survive longer than transduced peripheral-blood T-cells. To determine anti-tumor effects of transduced peripheral blood T-cells and EBV specific CTLs in vivo.

这个子项目是许多利用资源的研究子项目之一 由NIH/NCRR资助的中心拨款提供。子项目的主要支持 而子项目的主要调查员可能是由其他来源提供的， 包括其它NIH来源。 列出的子项目总成本可能 代表子项目使用的中心基础设施的估计数量， 而不是由NCRR赠款提供给子项目或子项目工作人员的直接资金。 目标 主要目的 评价向已被CD 45单克隆抗体（MAb）淋巴细胞耗竭的神经母细胞瘤患者施用递增剂量的14g2a.zeta嵌合受体转导的自体EBV特异性细胞毒性T淋巴细胞（EBV-CTL）和14g2a.zeta转导的自体外周血T细胞的安全性。 次要目的 确定这两种输注细胞类型在体内的差异存活和功能，特别是确定嵌合受体转导的EBV-CTL是否比转导的外周血T细胞存活更长。 确定转导的外周血T细胞和EBV特异性CTL的体内抗肿瘤作用。