Department of Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Canada.
Mol Ther. 2012 Jun;20(6):1148-57. doi: 10.1038/mt.2011.301. Epub 2012 Jan 24.
Replicating viruses for the treatment of cancer have a number of advantages over traditional therapeutic modalities. They are highly targeted, self-amplifying, and have the added potential to act as both gene-therapy delivery vehicles and oncolytic agents. Parapoxvirus ovis or Orf virus (ORFV) is the prototypic species of the Parapoxvirus genus, causing a benign disease in its natural ungulate host. ORFV possesses a number of unique properties that make it an ideal viral backbone for the development of a cancer therapeutic: it is safe in humans, has the ability to cause repeat infections even in the presence of antibody, and it induces a potent T(h)-1-dominated immune response. Here, we show that live replicating ORFV induces an antitumor immune response in multiple syngeneic mouse models of cancer that is mediated largely by the potent activation of both cytokine-secreting, and tumoricidal natural killer (NK) cells. We have also highlighted the clinical potential of the virus by demonstration of human cancer cell oncolysis including efficacy in an A549 xenograft model of cancer.
复制病毒用于癌症治疗具有许多优于传统治疗方式的优点。它们具有高度靶向性、自我扩增的特点,并且具有作为基因治疗载体和溶瘤剂的双重潜力。口疮病毒或羊口疮病毒(ORFV)是副痘病毒属的原型种,在其自然有蹄类宿主中引起良性疾病。ORFV 具有许多独特的特性,使其成为开发癌症治疗方法的理想病毒骨架:它在人类中是安全的,即使在存在抗体的情况下也具有重复感染的能力,并且它诱导强烈的 Th1 优势免疫反应。在这里,我们表明,活复制的 ORFV 在多种同种异体小鼠癌症模型中诱导抗肿瘤免疫反应,主要是通过强效激活细胞因子分泌和杀伤肿瘤的自然杀伤 (NK) 细胞来介导的。我们还通过证明人类癌细胞的溶瘤作用,包括在 A549 异种移植癌症模型中的疗效,突出了该病毒的临床潜力。