Chimeric T Cell for Therpay of Hodgkin Disease

用于治疗霍奇金病的嵌合 T 细胞

• 批准号: 8272438
• 负责人: Barbara Savoldo
• 金额: $ 30.9万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-07-01 至 2014-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8272438
• 关键词: Adoptive Transfer; Antibodies; Antigen Receptors; Antigen Targeting; Antigens; Applications Grants; Biopsy; CC chemokine receptor 4; CCL17 gene; CD28 gene; CD30 Antigens; CXCL10 gene; Cell physiology; Cells; Clinical; Clinical Data; Clinical Research; Clinical Trials; Cytokine Receptors; Cytotoxic T-Lymphocytes; Diffuse; Disease; Disease remission; EBV-Specific Cytotoxic T-Lymphocyte; Effectiveness; Effector Cell; Elements; Employee Strikes; Engineering; Environment; Growth; Growth Factor; Health; Hodgkin Disease; Homing; Human Herpesvirus 4; Immune; Immunotherapy; In Vitro; Individual; Injection of therapeutic agent; Interleukin-15; Lead; Maintenance; Malignant Neoplasms; Modification; Molecular; Monoclonal Antibodies; Patients; Production; Proteins; Refractory; Regulatory T-Lymphocyte; Relapse; SCID Mice; Site; Specificity; T cell differentiation; T cell therapy; T-Cell Receptor; T-Lymphocyte; TNFRSF8 gene; Testing; Toxic effect; Transgenic Organisms; Translating; Tumor Antigens; Ursidae Family; Variant; Viral Antigens; Viral Proteins; Xenograft Model; antibody conjugate; autocrine; base; cancer cell; cell motility; chemokine; chemokine receptor; cytokine; cytotoxic; effective therapy; experience; improved; in vivo; migration; mouse model; neoplastic cell; overexpression; paracrine; pre-clinical; preclinical study; prevent; receptor; response; success; suicide gene; tumor; validation studies; vector

DESCRIPTION (provided by applicant): Cytotoxic T-lymphocyte (CTL) therapy directed to Epstein-Barr virus (EBV) antigens has produced complete tumor responses in patients with EBV associated Hodgkin disease (HD) without toxicity. Many HD tumors, however, are EBV antigen negative. To extend immunotherapy to patients with such EBV negative HD, we propose to target the CD30 molecule, which is expressed by all malignant cells in both EBV positive and EBV negative HD. We hypothesize that we can exploit and extend the demonstrated effectiveness of EBV CTLs by redirecting them to the CD30 molecule, by forcing expression of a chimeric antigen receptor (CAR) targeting this molecule. We also hypothesize that we will be able to further engineer the CAR+ CTLs to overcome the molecular and cellular barriers that protect HD cells from immune attack. These hypotheses will be tested in three specific aims. In Aim 1, we propose to improve the homing of CAR+ CTLs to HD tumor cells by overexpressing the receptor (CCR4) for the chemokine TARC, which is constitutively produced by HD tumors, and whose receptor is lacking on CTLs. In Aim 2 we will evaluate whether expansion and persistence of our CCR4+ and CD30CAR+ CTLs is enhanced if these CTLs are further modified to produce their own growth cytokine (IL-15), which is essential to sustain their function. Finally, in Aim 3 we will analyze the interactions between regulatory T cells and our CAR+ CTLs. We will discover whether the modifications we have made allow the CAR+ CTLs to resist the inhibitory effects of the regulatory T cells that dominate sites of HD tumor, or whether alternative strategies will be required. The modifications we propose will be tested pre-clinically in vitro and in vivo and will form the basis of our continued clinical investigation of T- cell therapy for cancer. PUBLIC HEALTH RELEVANCE: We have had success in treating patients with relapsed Hodgkin disease (HD) by using their own immune cells directed to viral proteins that are often on the tumor cells. We now want to extend the application of this promising treatment by targeting other proteins that are on all HD cells, and by making the immune cells more potent.

描述（由申请人提供）：针对EB病毒（EBV）抗原的细胞毒性T淋巴细胞（CTL）治疗在EBV相关霍奇金病（HD）患者中产生了完全的肿瘤应答，且无毒性。然而，许多HD肿瘤是EBV抗原阴性的。为了将免疫疗法扩展到患有这种EBV阴性HD的患者，我们提出靶向CD 30分子，其由EBV阳性和EBV阴性HD中的所有恶性细胞表达。我们假设，我们可以利用和扩展EBV CTL的有效性，通过将它们重定向到CD 30分子，通过强制表达靶向该分子的嵌合抗原受体（CAR）。我们还假设，我们将能够进一步工程化CAR+ CTL，以克服保护HD细胞免受免疫攻击的分子和细胞屏障。这些假设将在三个具体目标中得到检验。在目的1中，我们提出通过过表达趋化因子TARC的受体（CCR 4）来改善CAR+ CTL向HD肿瘤细胞的归巢，所述趋化因子TARC由HD肿瘤组成性产生，并且其受体在CTL上缺乏。在目标2中，我们将评估如果我们的CCR 4+和CD 30 CAR + CTL被进一步修饰以产生其自身的生长细胞因子（IL-15），则这些CTL的扩增和持久性是否得到增强，这对于维持其功能至关重要。最后，在目标3中，我们将分析调节性T细胞与我们的CAR+ CTL之间的相互作用。我们将发现我们所做的修饰是否允许CAR+ CTL抵抗主导HD肿瘤部位的调节性T细胞的抑制作用，或者是否需要替代策略。我们提出的修饰将在体外和体内进行临床前测试，并将形成我们对癌症T细胞疗法的持续临床研究的基础。 公共卫生相关性：我们已经成功地治疗了复发性霍奇金病（HD）患者，方法是使用他们自己的免疫细胞针对肿瘤细胞上的病毒蛋白。我们现在希望通过靶向所有HD细胞上的其他蛋白质并使免疫细胞更有效来扩展这种有希望的治疗方法的应用。