Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N, E5-110, Seattle, WA 98109, USA; Department of Laboratory Medicine, University of Washington, Seattle, WA 98195, USA.
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N, E5-110, Seattle, WA 98109, USA.
Virology. 2014 Apr;454-455:353-61. doi: 10.1016/j.virol.2013.12.037. Epub 2014 Jan 31.
Treatment for most persistent viral infections consists of palliative drug options rather than curative approaches. This is often because long-lasting viral DNA in infected cells is not affected by current antivirals, providing a source for viral persistence and reactivation. Targeting latent viral DNA itself could therefore provide a basis for novel curative strategies. DNA cleavage enzymes can be used to induce targeted mutagenesis of specific genes, including those of exogenous viruses. Although initial in vitro and even in vivo studies have been carried out using DNA cleavage enzymes targeting various viruses, many questions still remain concerning the feasibility of these strategies as they transition into preclinical research. Here, we review the most recent findings on DNA cleavage enzymes for human viral infections, consider the most relevant animal models for several human viral infections, and address issues regarding safety and enzyme delivery. Results from well-designed in vivo studies will ideally provide answers to the most urgent remaining questions, and allow continued progress toward clinical application.
针对大多数持续性病毒感染的治疗方法是姑息性药物选择,而不是治疗方法。这通常是因为感染细胞中持久存在的病毒 DNA 不受现有抗病毒药物的影响,为病毒的持续存在和重新激活提供了来源。因此,针对潜伏病毒 DNA 本身可以为新的治疗策略提供基础。DNA 切割酶可用于诱导针对特定基因(包括外源病毒基因)的靶向突变。尽管已经使用针对各种病毒的 DNA 切割酶进行了初步的体外甚至体内研究,但在将这些策略转化为临床前研究时,仍有许多问题需要考虑这些策略的可行性。在这里,我们回顾了针对人类病毒感染的 DNA 切割酶的最新发现,考虑了几种人类病毒感染的最相关动物模型,并讨论了安全性和酶传递方面的问题。精心设计的体内研究结果将理想地为最紧迫的剩余问题提供答案,并为临床应用的持续进展提供帮助。