Ther Clin Risk Manag. 2006 Sep;2(3):259-69. doi: 10.2147/tcrm.2006.2.3.259.
Persistent infection by 'high risk' genotypes of human papilloma virus (HPV) is necessary but not sufficient for the development of over 98% of cervical cancers. Thus the development of vaccines that prevent HPV transmission represent an important opportunity to prevent cervical cancer. There are several prophylactic HPV vaccine formulations based upon L1 virus-like particles (VLPs) currently in phase III trials and recently released data are extremely promising. However, many practical issues surrounding implementation of these vaccines need to be addressed including, who and when to vaccinate, duration of protection, and integration with current screening programs. The vaccines currently being evaluated target the two most prevalent high risk HPV types which are responsible for approximately 70% of cervical cancers. To increase the breadth of protection, it is likely that L1 VLPs of other viral subtypes must be included, although vaccines targeting the conserved regions of the L2 minor capsid protein warrant further exploration in this regard. In addition the vaccines nearing licensing will not combat established HPV-related disease and a therapeutic vaccine, of which there are several candidates in early stages of development, would be desirable. This review discusses the background to and progress in vaccine development and the issues surrounding the introduction of HPV vaccines.
高危型人乳头瘤病毒(HPV)的持续感染是导致 98%以上宫颈癌发展的必要条件,但不是充分条件。因此,开发预防 HPV 传播的疫苗是预防宫颈癌的重要机会。目前有几种基于 L1 病毒样颗粒(VLPs)的预防性 HPV 疫苗制剂正在进行 III 期临床试验,最近公布的数据非常有希望。然而,在实施这些疫苗方面还需要解决许多实际问题,包括接种对象和时间、保护期限以及与现有筛查计划的结合。目前正在评估的疫苗针对两种最常见的高危 HPV 类型,它们约占宫颈癌的 70%。为了增加保护范围,很可能需要包含其他病毒亚型的 L1 VLP,尽管针对 L2 次要衣壳蛋白保守区的疫苗在这方面值得进一步探索。此外,即将获得许可的疫苗不能治疗已确立的 HPV 相关疾病,因此需要一种治疗性疫苗,目前有几种候选疫苗处于早期开发阶段。这篇综述讨论了疫苗开发的背景、进展以及 HPV 疫苗引入所面临的问题。