Oncolytic herpes simplex virus immunovirotherapy in combination with immune checkpoint blockade to treat glioblastoma

被引:71
作者
Saha, Dipongkor [1 ,2 ,3 ]
Martuza, Robert L. [1 ,2 ,3 ]
Rabkin, Samuel D. [1 ,2 ,3 ]
机构
[1] Massachusetts Gen Hosp, Dept Neurosurg, Mol Neurosurg Lab, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Brain Tumor Res Ctr, Boston, MA 02114 USA
[3] Harvard Med Sch, Boston, MA 02114 USA
关键词
cancer immunotherapy; cancer stem cells; checkpoint inhibitors; glioma; HSV; immunovirotherapy; macrophage polarization; oncolytic virus; PD-1; BLOCKADE; STEM-CELLS; CANCER-IMMUNOTHERAPY; MISMATCH REPAIR; BRAIN-TUMORS; SOLID TUMORS; THERAPY; MELANOMA; MODELS; GLIOMA;
D O I
10.2217/imt-2018-0009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:779 / 786
页数:8
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