Department of Neurosurgery, Molecular Neurosurgery Laboratory & Brain Tumor Research Center, Massachusetts General Hospital & Harvard Medical School, Boston, MA 02114, USA.
Immunotherapy. 2018 Jul;10(9):779-786. doi: 10.2217/imt-2018-0009.
Oncolytic viruses, such as oncolytic herpes simplex virus (oHSV), are a new class of cancer therapeutic, which selectively replicate and kill cancer cells, while inducing an inflammatory microenvironment, immunovirotherapy. Recently, an oHSV (talimogene laherparepvec) has been approved for the treatment of advanced melanoma. Glioblastoma (GBM) is an almost always lethal primary tumor in the brain that is highly immunosuppressive, and posited to contain GBM stem-like cells (GSCs). Immune checkpoint blockade has revolutionized therapy for some cancers, but not GBM. We have used a syngeneic GSC-derived orthotopic GBM model (005) to develop immunotherapeutic strategies. Curative therapy required oHSV expressing IL-12 in combination with two checkpoint inhibitors, anti-PD-1 and anti-CTLA-4. This response required CD4 and CD8 T cells, and macrophages in a complex interplay.
溶瘤病毒,如溶瘤单纯疱疹病毒(oHSV),是一类新型的癌症治疗药物,可选择性复制并杀死癌细胞,同时诱导炎症微环境,即免疫病毒疗法。最近,一种 oHSV(talimogene laherparepvec)已被批准用于治疗晚期黑色素瘤。胶质母细胞瘤(GBM)是一种几乎总是致命的脑内原发性肿瘤,具有高度免疫抑制性,并被认为包含胶质母细胞瘤干细胞样细胞(GSCs)。免疫检查点阻断已彻底改变了一些癌症的治疗方法,但对 GBM 没有效果。我们使用了源自同种异体 GSC 的原位 GBM 模型(005)来开发免疫治疗策略。治愈性治疗需要表达 IL-12 的 oHSV 与两种检查点抑制剂(抗 PD-1 和抗 CTLA-4)联合使用。这种反应需要 CD4 和 CD8 T 细胞以及巨噬细胞的复杂相互作用。