School of Medicine, University of Leeds, Leeds, UK.
Division of Radiotherapy and Imaging, Institute of Cancer Research, London, UK.
J Immunother Cancer. 2021 Mar;9(3). doi: 10.1136/jitc-2020-001143.
Patients with glioblastoma (GBM) have a poor prognosis, and inefficient delivery of drugs to tumors represents a major therapeutic hurdle. Hematopoietic stem cell (HSC)-derived myeloid cells efficiently home to GBM and constitute up to 50% of intratumoral cells, making them highly appropriate therapeutic delivery vehicles. Because myeloid cells are ubiquitously present in the body, we recently established a lentiviral vector containing matrix metalloproteinase 14 (MMP14) promoter, which is active specifically in tumor-infiltrating myeloid cells as opposed to myeloid cells in other tissues, and resulted in a specific delivery of transgenes to brain metastases in HSC gene therapy. Here, we used this novel approach to target transforming growth factor beta (TGFβ) as a key tumor-promoting factor in GBM. Transplantation of HSCs transduced with lentiviral vector expressing green fluorescent protein (GFP) into lethally irradiated recipient mice was followed by intracranial implantation of GBM cells. Tumor-infiltrating HSC progeny was characterized by flow cytometry. In therapy studies, mice were transplanted with HSCs transduced with lentiviral vector expressing soluble TGFβ receptor II-Fc fusion protein under MMP14 promoter. This TGFβ-blocking therapy was compared with the targeted tumor irradiation, the combination of the two therapies, and control. Tumor growth and survival were quantified (statistical significance determined by t-test and log-rank test). T cell memory response was probed through a repeated tumor challenge. Myeloid cells were the most abundant HSC-derived population infiltrating GBM. TGFβ-blocking HSC gene therapy in combination with irradiation significantly reduced tumor burden as compared with monotherapies and the control, and significantly prolonged survival as compared with the control and TGFβ-blocking monotherapy. Long-term protection from GBM was achieved only with the combination treatment (25% of the mice) and was accompanied by a significant increase in CD8+ T cells at the tumor implantation site following tumor rechallenge. We demonstrated a preclinical proof-of-principle for tumor myeloid cell-specific HSC gene therapy in GBM. In the clinic, HSC gene therapy is being successfully used in non-cancerous brain disorders and the feasibility of HSC gene therapy in patients with glioma has been demonstrated in the context of bone marrow protection. This indicates an opportunity for clinical translation of our therapeutic approach.
胶质母细胞瘤(GBM)患者预后较差,药物向肿瘤的递送效率低下是主要的治疗障碍。造血干细胞(HSC)衍生的髓样细胞能够有效地归巢至 GBM 并构成肿瘤内细胞的 50%,使其成为非常合适的治疗性递药载体。由于髓样细胞在体内普遍存在,我们最近建立了一种含有基质金属蛋白酶 14(MMP14)启动子的慢病毒载体,该启动子在肿瘤浸润性髓样细胞中特异性活跃,而在其他组织中的髓样细胞中不活跃,从而实现了 HSC 基因治疗中脑转移的转基因的特异性递药。在此,我们使用这种新方法来靶向转化生长因子β(TGFβ),将其作为 GBM 中的关键促肿瘤因子。将表达绿色荧光蛋白(GFP)的慢病毒载体转导的 HSC 移植到致死性辐照的受体小鼠中,然后进行 GBM 细胞颅内植入。通过流式细胞术对肿瘤浸润性 HSC 祖细胞进行了表征。在治疗研究中,将表达可溶性 TGFβ受体 II-Fc 融合蛋白的慢病毒载体转导的 HSC 移植到小鼠中,该载体受 MMP14 启动子调控。将这种 TGFβ 阻断治疗与靶向肿瘤照射、两种疗法的联合以及对照进行了比较。通过 t 检验和对数秩检验确定了肿瘤生长和存活的定量(统计学意义)。通过重复肿瘤挑战探测 T 细胞记忆反应。髓样细胞是浸润 GBM 的最丰富的 HSC 衍生群体。与单独治疗和对照相比,TGFβ 阻断的 HSC 基因治疗联合照射可显著降低肿瘤负担,并可显著延长存活时间。仅联合治疗(25%的小鼠)可实现对 GBM 的长期保护,并且在肿瘤再挑战时,肿瘤植入部位的 CD8+T 细胞显著增加。我们在 GBM 中证明了肿瘤髓样细胞特异性 HSC 基因治疗的临床前原理验证。在临床上,HSC 基因治疗正在成功用于非癌性脑疾病,并且在骨髓保护的背景下已经证明了 HSC 基因治疗在脑胶质瘤患者中的可行性。这表明我们的治疗方法具有临床转化的机会。