Department of Pathology and Molecular Medicine, McMaster Immunology Research Centre, Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario L8S4K1, Canada.
SillaJen Biotherapeutics, San Francisco, California 94111, USA.
Nat Rev Cancer. 2014 Aug;14(8):559-67. doi: 10.1038/nrc3770. Epub 2014 Jul 3.
Recent clinical data have emphatically shown the capacity of our immune systems to eradicate even advanced cancers. Although oncolytic viruses (OVs) were originally designed to function as tumour-lysing therapeutics, they have now been clinically shown to initiate systemic antitumour immune responses. Cell signalling pathways that are activated and promote the growth of tumour cells also favour the growth and replication of viruses within the cancer. The ability to engineer OVs that express immune-stimulating 'cargo', the induction of immunogenic tumour cell death by OVs and the selective targeting of OVs to tumour beds suggests that they are the ideal reagents to enhance antitumour immune responses. Coupling of OV therapy with tumour antigen vaccination, immune checkpoint inhibitors and adoptive cell therapy seems to be ready to converge towards a new generation of multimodal therapeutics to improve outcomes for cancer patients.
最近的临床数据有力地表明,我们的免疫系统有能力根除甚至晚期癌症。虽然溶瘤病毒(OVs)最初被设计为具有肿瘤杀伤作用的治疗药物,但现在已经在临床上证明它们可以引发系统性抗肿瘤免疫反应。激活并促进肿瘤细胞生长的细胞信号通路也有利于病毒在癌症中的生长和复制。能够设计表达免疫刺激“货物”的 OVs,通过 OVs 诱导免疫原性肿瘤细胞死亡,以及对肿瘤床的 OVs 选择性靶向,这表明它们是增强抗肿瘤免疫反应的理想试剂。将 OV 治疗与肿瘤抗原疫苗接种、免疫检查点抑制剂和过继细胞疗法相结合,似乎已经准备好融合为新一代的多模式治疗方法,以改善癌症患者的预后。
Nat Rev Cancer. 2014-7-3
EBioMedicine. 2016-7
Cancer Immunol Res. 2014-4
Expert Opin Biol Ther. 2015-7
J Cell Physiol. 2018-8-26
J Immunother Cancer. 2019-1-9
Int J Nanomedicine. 2025-8-16
Front Med. 2025-7-14
Vet Comp Oncol. 2025-3
Int J Mol Sci. 2024-10-16
Nat Biotechnol. 2014-1-26
Mol Ther. 2013-10-25
Nat Rev Microbiol. 2013-12-2
Immunotherapy. 2013-11
Oncoimmunology. 2013-7-1
Oncoimmunology. 2013-6-1
Nat Rev Cancer. 2013-8