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Present status of human papillomavirus vaccine development and implementation

机译:人乳头瘤病毒疫苗的开发和实施现状

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Oncogenic human papillomavirus (HPV) infection is the cause of nearly all cervical cancers and a proportion of other anogenital and oropharyngeal cancers. A bivalent vaccine containing HPV 16 and 18 and a quadrivalent vaccine containing HPV 6, 11, 16, and 18 antigens are in use in vaccination programmes around the world. In clinical trials, three vaccine doses provided 90-100% protection against cervical infection and pre-cancer related to HPV 16 and 18 in women aged 15-26 years who were not infected at vaccination. Partial cross-protection against other HPV types has been reported but its duration is unknown. The vaccines were also efficacious at the prevention of HPV 16 and 18 infections at other anatomical sites in both sexes. Immunobridging studies allowed licensing of the vaccines for use starting at age 9 years for both sexes. Two-dose schedules elicit high antibody concentrations, leading to the recommendation of two-dose schedules for girls aged 9-14 years. Pre-licensure and post-licensure studies have provided data supporting vaccine safety. In 2014, a nonavalent vaccine containing HPV 6, 11, 16, 18, 31, 33, 45, 52, and 58 antigens was licensed by the US Food and Drug Administration. HPV vaccination was first introduced in high-income countries owing to vaccine cost, logistic challenges, and competing health priorities. Since 2011, vaccine prices have lowered, allowing the introduction of the vaccine in some middle-income countries. Funding of the vaccine by the GAVI Alliance in 2012 led to demonstration projects in some low-income countries. By 2014, more than 57 countries had included the HPV vaccine in their national health programmes. Data from several countries have shown the effect of vaccination on HPV infection and associated disease, and provided evidence of herd immunity. Expansion of programmes to countries with the highest burden of disease is beginning, but further efforts are needed to realise the potential of HPV vaccines.
机译:致癌性人乳头瘤病毒(HPV)感染是几乎所有子宫颈癌以及一部分其他肛门生殖器和口咽癌的病因。包含HPV 16和18的二价疫苗和包含HPV 6、11、16和18抗原的四价疫苗正在全世界的疫苗接种计划中使用。在临床试验中,在未接种疫苗的15-26岁女性中,三种疫苗剂量可提供90-100%的预防宫颈感染和与HPV 16和18相关的癌症前期保护。已经报道了针对其他HPV类型的部分交叉保护作用,但持续时间未知。该疫苗还有效预防了男女两性在其他解剖部位的HPV 16和18感染。免疫封闭研究允许从9岁开始为两性使用该疫苗。两次给药计划会引起高抗体浓度,因此建议对9-14岁的女孩推荐两次给药计划。许可前和许可后研究提供了支持疫苗安全性的数据。 2014年,包含HPV 6、11、16、18、31、33、45、52和58抗原的非价疫苗获得了美国食品和药物管理局的许可。由于疫苗成本高,后勤挑战和卫生优先事项相互竞争,HPV疫苗最初是在高收入国家引入的。自2011年以来,疫苗价格降低,从而使某些中等收入国家可以使用该疫苗。 GAVI联盟在2012年为疫苗提供了资金,在一些低收入国家开展了示范项目。到2014年,超过57个国家已将HPV疫苗纳入其国家卫生计划。来自几个国家的数据显示了疫苗接种对HPV感染和相关疾病的影响,并提供了牛群免疫的证据。开始将计划扩展到疾病负担最重的国家,但需要进一步努力以实现HPV疫苗的潜力。

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