Cell lineage as an indicator of immune response in neuroblastoma

细胞谱系作为神经母细胞瘤免疫反应的指标

• 批准号: 10467445
• 负责人: Rani E. George
• 金额: $ 40.54万
• 依托单位: DANA-FARBER CANCER INST
• 依托单位国家: 美国
• 财政年份: 2022
• 资助国家: 美国
• 起止时间: 2022-06-16 至 2027-05-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10467445
• 关键词: Address; Adoptive Immunotherapy; Adoptive Transfer; Adrenergic Agents; Affect; Antibodies; Antigens; Biological Markers; CD94 Antigen; Cell Lineage; Cell Therapy; Cells; Characteristics; Childhood Extracranial Solid Tumor; Childhood Solid Neoplasm; Clinical Trials Design; Cluster Analysis; Complex; Cytotoxic T-Lymphocytes; Data Set; Development; Epigenetic Process; Exhibits; Gene Activation; Gene Expression Profile; Genes; Goals; Heterogeneity; Immune; Immune Evasion; Immune Response Genes; Immune response; Immune system; Immunologics; Immunotherapy; In Vitro; Infiltration; Inflammatory Response; Licensing; Ligands; MYCN gene; Malignant Childhood Neoplasm; Malignant Neoplasms; Mediating; Mesenchymal; Mesenchymal Cell Neoplasm; Modeling; Molecular; Monoclonal Antibodies; Mutation; NK Cell Activation; NK cell therapy; Natural Killer Cells; Neural Crest; Neuroblastoma; Neurons; Oncogenes; Patient Selection; Patients; Phenotype; Population; Primary Neoplasm; Property; Regimen; Repression; Research Proposals; Resistance; Role; Sampling; Shapes; T cell therapy; T-Lymphocyte; Testing; Translating; Tumor Suppression; Tumor-infiltrating immune cells; Undifferentiated; Up-Regulation; anti-tumor immune response; cancer cell; design; epigenetic silencing; genetic signature; high risk; humanized mouse; immune activation; immune checkpoint blockade; immunogenic; immunogenicity; immunoregulation; improved; in vivo; in vivo Model; innate immune sensing; innovation; neoplastic cell; neuroblastoma cell; patient stratification; pre-clinical; receptor; response; single-cell RNA sequencing; success; transcription factor; treatment response; treatment strategy; tumor; tumor growth; tumor microenvironment

PROJECT SUMMARY/ABSTRACT The sparse landscape of targetable mutations in pediatric cancers in general and neuroblastoma (NB) in particular, together with the recent successes of the anti-GD2 antibody, dinutuximab (2), provides a compelling rationale for further development of immune-based treatment strategies against this devastating cancer. However, responses to adoptive immunotherapy and checkpoint blockade have met with limited success, partly due to an incomplete understanding of the mechanisms underlying immune responsiveness or resistance in this tumor marked by significant heterogeneity. We undertook an unbiased clustering analysis of transcriptional signatures derived from a large primary NB data set and identified a subset of tumors, characterized by the high expression of immune response activation and suppression genes, and indicating the potential for eliciting an anti-tumor immune response. These signatures were seen mainly in tumors of the mesenchymal (MES) lineage, one of the two epigenetically regulated cell states in NB, comprised of undifferentiated malignant cells with primitive neural crest-like properties. By contrast, tumors with committed, adrenergic (ADR) neuron-like malignant cells were less immunogenic and exhibited PRC2-mediated suppression of key tumor cell-intrinsic immune activation genes. These promising results led to our central hypothesis that cell lineage state is an important predictor of immune therapy response in NB. In Aim 1, we will elucidate the epigenetic mechanisms underlying lineage-specific activation of immune response genes. Aim 2 will assess lineage- dependent functions of cytotoxic T cells in tumor control by determining whether MES NB cells possess an inflamed TME that facilitates cell-based therapies. In Aim 3, we will determine whether the increased expression of NK cell receptor ligands in MES tumors translates into response to NK cell therapy and whether PRC2 inhibition will augment such responses in ADR tumors alone or in combination dinutuximab. Together, these studies are expected to provide a compelling rationale for the use of tumor cell lineage for the selection of patients who are most likely to benefit from immunotherapy and to pre-clinically validate treatment strategies involving combinations of epigenetic and immune-based therapies to target the specific immune evasion mechanisms deployed by NB cells, our long-term goal.

项目摘要/摘要 儿童普通癌症和神经母细胞瘤(NB)中靶向突变的稀疏格局 特别是，加上最近成功的抗GD2抗体，地诺昔单抗(2)，提供了一种令人信服的 进一步开发基于免疫的治疗策略以对抗这种毁灭性的癌症的理论基础。 然而，对过继免疫疗法和检查站封锁的反应取得的成功有限，部分原因是 由于对其免疫应答或抵抗机制的不完全理解 以显著异质性为特征的肿瘤。我们对转录因子进行了无偏聚类分析。 从大型主NB数据集派生的签名 确定了肿瘤的一个子集，特征是高 免疫反应激活和抑制基因的表达，并表明可能引发 抗肿瘤免疫反应。这些特征主要见于间充质(MES)谱系的肿瘤， NB中受表观遗传调控的两种细胞状态之一，由未分化的恶性细胞组成 原始的神经冠状特征。相比之下，具有承诺、肾上腺素能(ADR)神经元样细胞的肿瘤 恶性细胞的免疫原性较低，并表现出PRC2介导的对关键肿瘤细胞固有的抑制 免疫激活基因。这些有希望的结果导致了我们的中心假设，即细胞谱系状态是一种 神经母细胞瘤免疫治疗反应的重要预测因子。在目标1中，我们将阐明表观遗传学 免疫反应基因谱系特异性激活的潜在机制。目标2将评估血统- 细胞毒性T细胞在肿瘤控制中的依赖功能：确定MES-NB细胞是否具有 发炎的TME促进了基于细胞的治疗。在目标3中，我们将确定增加的表达是否 在MES肿瘤中NK细胞受体配体的表达转化为对NK细胞治疗的应答，以及PRC2 抑制将增强ADR肿瘤的这种反应，或与地诺昔单抗联合使用。加在一起，这些 研究有望为使用肿瘤细胞谱系选择患者提供令人信服的理由。 谁最有可能从免疫疗法中受益，并在临床前验证治疗策略，包括 表观遗传和基于免疫的治疗相结合，以靶向特定的免疫逃避机制 由NB细胞部署，是我们的长期目标。