World Health Organization, 20, Avenue Appia, 1211, Geneva 27, Switzerland.
Vaccine. 2012 Dec 17;31(1):3-11. doi: 10.1016/j.vaccine.2012.04.104. Epub 2012 May 17.
Data on duration and long-term protective effects of hepatitis A vaccines (HepA) have not been reviewed using a systematic approach. Our objective is to provide a comprehensive review of evidence on the duration of protection achieved by HepA, which is needed for revising existing vaccine policies. Limitations in data availability and implications for future research in this area are discussed.
A systematic literature review was conducted including all studies published between 1997 and 2011 reporting on long-term protection of HepA. The outcomes considered were hepatitis A virus (HAV) infection and sero-protection measured by anti-HAV antibodies after follow-up times of over 5 years post-vaccination.
299 studies were identified from MEDLINE and 51 studies from EMBASE. 13 manuscripts met our inclusion criteria. The maximum observation times and reported persistence levels of sero-protective anti-HAV antibodies was 15 years for live attenuated HepA and 14 years for inactivated HepA. All data were from observational studies and showed that higher number of doses of live attenuated vaccine led to higher seropositivity and GMT, but dosage and schedule did not significantly impact the long-term protection following inactivated vaccine. Few comparisons were made between the two vaccine types indicating highest levels of antibody titers achieved by multiple doses of live attenuated vaccines 7 years post-vaccination.
Available data indicate that both inactivated and live attenuated HepA are capable of providing protection up to 15 years as defined by currently accepted, conservative correlates of protection. Further investigations are needed to continue to monitor the long-term protection afforded by these vaccines. Standardized methods are required for vaccine-follow-up studies including assessment of co-variables potentially affecting long-term protection.
尚未采用系统方法来评估甲型肝炎疫苗(HepA)的持续时间和长期保护效果。我们的目的是全面回顾 HepA 可实现的保护持续时间方面的证据,这是修订现有疫苗政策所必需的。讨论了数据获取方面的局限性以及对该领域未来研究的影响。
对 1997 年至 2011 年间发表的所有关于 HepA 长期保护的研究进行了系统文献回顾,报告了随访时间超过 5 年的甲型肝炎病毒(HAV)感染和血清保护情况。
从 MEDLINE 中确定了 299 项研究,从 EMBASE 中确定了 51 项研究。有 13 篇文献符合纳入标准。活疫苗和灭活疫苗的最长观察时间和报告的保护性抗-HAV 抗体持续时间分别为 15 年和 14 年。所有数据均来自观察性研究,表明活疫苗接种剂量越高,血清阳性率和 GMT 越高,但剂量和方案对接种灭活疫苗后的长期保护作用没有显著影响。两种疫苗类型之间的比较很少,表明活疫苗多次接种可获得最高水平的抗体滴度,在接种后 7 年达到最高水平。
现有数据表明,灭活疫苗和减毒活疫苗都能提供长达 15 年的保护,这是目前公认的保护性相关指标所定义的。需要进一步调查以继续监测这些疫苗提供的长期保护。疫苗随访研究需要采用标准化方法,评估可能影响长期保护的协变量。