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为18岁以上女性接种预防性人乳头瘤病毒疫苗。

Prophylactic HPV vaccination for women over 18 years of age.

作者信息

Adams M, Jasani B, Fiander A

机构信息

Velindre Cancer Centre, Whitchurch, Cardiff, Wales CF14 2TL, UK.

出版信息

Vaccine. 2009 May 26;27(25-26):3391-4. doi: 10.1016/j.vaccine.2009.01.067. Epub 2009 Feb 5.

Abstract

Cervical screening has resulted in a major reduction in the incidence and mortality of cervical cancer in the UK and other developed countries. Nevertheless approximately 2700 women present with cervical cancer in the UK each year with mortality in excess of 1000 cases. Prophylactic HPV vaccination against HPV 16 and 18 has been shown to be highly effective in preventing HPV related malignancy in clinical trials. Newly introduced HPV vaccination programmes in the UK and elsewhere are ultimately likely to result in a further significant reduction in the incidence and mortality of cervical cancer. These vaccination programmes will be most effective in early adolescence when prevalence of HPV infection is low. Consequently, vaccination programmes in the UK have been initially targeted at 12 to 13-year olds. In Australia favourable estimates of cost effectiveness have supported funding of a 'catch-up' programme to 26 years. In the UK the catch up programme has for the present been restricted to 18 years for cost effectiveness reasons. In addition the value of HPV vaccination beyond 26 years has not yet been fully clarified. Nevertheless women up to 45 years of age have been shown to exhibit strong immune responses to the bivalent HPV vaccine which might be expected to reduce the risk of HPV re-infection and address the second peak of HPV related malignancy in later life, evident over 45 years of age. Early data from randomised trials testing the quadrivalent HPV vaccine in women over 25 years has suggested high vaccine efficacy comparable to younger women. This paper will explore the evidence supporting HPV vaccination in HPV naïve and HPV exposed sexually active women up to 26 years and beyond this age group.

摘要

子宫颈癌筛查已使英国和其他发达国家的子宫颈癌发病率和死亡率大幅降低。然而,英国每年仍有大约2700名女性被诊断为子宫颈癌,死亡人数超过1000例。在临床试验中,针对人乳头瘤病毒16型和18型的预防性人乳头瘤病毒疫苗已被证明在预防人乳头瘤病毒相关恶性肿瘤方面非常有效。英国和其他地方新推出的人乳头瘤病毒疫苗接种计划最终可能会使子宫颈癌的发病率和死亡率进一步大幅降低。这些疫苗接种计划在人乳头瘤病毒感染率较低的青春期早期最为有效。因此,英国的疫苗接种计划最初针对的是12至13岁的青少年。在澳大利亚,对成本效益的有利估计支持了一项针对26岁人群的“补种”计划的资金投入。在英国,由于成本效益的原因,目前补种计划仅限于18岁。此外,26岁以上人群接种人乳头瘤病毒疫苗的价值尚未完全明确。然而,已证明45岁以下的女性对二价人乳头瘤病毒疫苗表现出强烈的免疫反应,这可能会降低人乳头瘤病毒再次感染的风险,并应对45岁以上明显出现的人乳头瘤病毒相关恶性肿瘤的第二个高峰。在25岁以上女性中测试四价人乳头瘤病毒疫苗的随机试验的早期数据表明,疫苗效力与年轻女性相当。本文将探讨支持在26岁及以上未感染人乳头瘤病毒和已感染人乳头瘤病毒的性活跃女性中接种人乳头瘤病毒疫苗的证据。

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