Egawa Nagayasu, Doorbar John
Department of Pathology, Tennis Court Road, University of Cambridge, Cambridge, UK.
Department of Pathology, Tennis Court Road, University of Cambridge, Cambridge, UK.
Virus Res. 2017 Mar 2;231:119-127. doi: 10.1016/j.virusres.2016.12.017. Epub 2016 Dec 28.
Human Papillomavirus (HPV) research has been dominated by the study of a subset of Alpha papillomaviruses that together cause almost 5% of human cancers worldwide, with the focus being on the two most prominent of these (HPV16 and 18). These viruses are referred to as 'high-risk' (hrHPV), to distinguish them from the over 200 prevalent HPV types that more commonly cause only benign epithelial lesions. The 'low-risk' (lrHPV) term used to describe this group belies their cumulative morbidity. Persistent laryngeal papillomas, which occur rarely in children and adults, require regular surgical de-bulking to allow breathing. Such infections are not curable, and despite being caused by HPV11 (a lrHPV) are associated with 1-3% risk of cancer progression if not resolved. Similarly, the ubiquitous Beta HPV types, which commonly cause asymptomatic infections at cutaneous sites, can sometimes cause debilitating papillomatosis with associated cancer risk. Recalcitrant genital warts, which affect 1 in 200 young adults in the general population, and even the ubiquitous common warts and verrucas that most of us at some time experience, cannot be reliably eradicated, with treatment strategies advancing little over the last 100 years. The review highlights molecular similarities between high and low-risk HPV types, and focuses on the different pathways that the two groups use to ensure persistent infection and adequate virus shedding from the epithelial surface. Understanding the normal patterns of viral gene expression that underlie lesion formation, and which also prevent loss of the infected basal cells in established lesions, are particularly important when considering new treatment options. Finally, the common requirement for deregulated viral gene expression and genome persistence in development of cancers, unites both high and low-risk HPV types, and when considered alongside viral protein functions, provides us with a working understanding of the mechanisms that underlie HPV-associated pathology.
人乳头瘤病毒(HPV)研究一直以α乳头瘤病毒亚群的研究为主导,这些病毒共同导致了全球近5%的人类癌症,研究重点是其中最突出的两种(HPV16和18)。这些病毒被称为“高危”(hrHPV),以区别于另外200多种常见的HPV类型,后者通常仅引起良性上皮病变。用于描述这一组的“低危”(lrHPV)术语掩盖了它们累积的发病率。持续性喉乳头瘤在儿童和成人中很少见,需要定期手术切除以保证呼吸。这种感染无法治愈,尽管是由HPV11(一种低危型HPV)引起的,但如果不解决,有1%-3%的癌症进展风险。同样,普遍存在的β型HPV通常在皮肤部位引起无症状感染,有时会导致使人衰弱的乳头瘤病,并伴有癌症风险。难治性生殖器疣影响普通人群中每200名年轻人中的1人,甚至我们大多数人在某个时候都会经历的普遍存在的普通疣和跖疣,也无法可靠地根除,在过去100年里治疗策略进展甚微。该综述强调了高危和低危HPV类型之间的分子相似性,并重点关注两组病毒用于确保持续感染和从上皮表面充分排出病毒的不同途径。在考虑新的治疗方案时,了解病变形成基础的病毒基因表达正常模式,以及这种模式如何防止已形成病变中受感染基底细胞的丢失,尤为重要。最后,癌症发展过程中对病毒基因表达失调和基因组持久性的共同要求,将高危和低危HPV类型联系在一起,结合病毒蛋白功能来考虑,能让我们对HPV相关病理学的潜在机制有一个实际的了解。