Institute of Medical Biology, Chinese Academy of Medical Sciences, Peking Union Medical College, Kunming, China; Yunnan Key Laboratory of Vaccine Research and Development on Severe Infectious Diseases, Kunming, China; Yunnan Provincial Key Laboratory of Vector-borne Diseases Control and Research, Kunming, China; Kunming Medical University Haiyuan College, Kunming, China.
Institute of Medical Biology, Chinese Academy of Medical Sciences, Peking Union Medical College, Kunming, China; Yunnan Key Laboratory of Vaccine Research and Development on Severe Infectious Diseases, Kunming, China; Yunnan Provincial Key Laboratory of Vector-borne Diseases Control and Research, Kunming, China.
Clin Microbiol Infect. 2019 Nov;25(11):1422-1427. doi: 10.1016/j.cmi.2018.11.005. Epub 2018 Nov 27.
Both live attenuated (HA-L) and inactivated (HA-I) hepatitis A vaccine were licensed for routine use in China. Although phase 1, 2 and 3 clinical studies of both vaccines have been completed, further systematic evaluation of their immunogenicity and immunological persistence under phase 4 clinical studies in a wide range of conditions and involving large populations is necessary. A phase IV clinical trial (NCT02601040) was performed in 9000 participants over 18 months of age. Geometric mean concentrations (GMCs) and seroconversion rates (SRs) were compared at five time points during 3 years for 1800 individuals among them. The SRs of HA-L and HA-I were 98.08% (95% CI 95.59%-99.38%) and 99.64% (95% CI 98.93%-100.00%) respectively 28 days after administration of the first dose, and remained at 97.07% (95% CI 94.31%-98.73%) or above and 96.73% (95% CI 94.07%-98.42%) or above respectively during the following 3 years. The GMCs for both the HA-L and HA-I groups showed that both vaccines elicited high anti-HAV titres, considerably more than the threshold of protection needed against HAV infection in humans, and these titres were sustained. Hence, both HA-I and HA-L vaccines could provide an excellent long-term protective effect, and supported the routine use of both vaccines.
两种减毒活(HA-L)和灭活(HA-I)甲型肝炎疫苗均已获得许可在中国常规使用。尽管这两种疫苗的 1 期、2 期和 3 期临床试验已经完成,但仍需要在更广泛的条件和更大人群中进行 4 期临床试验,以进一步系统评估其免疫原性和免疫持久性。一项 4 期临床试验(NCT02601040)在 18 个月以上的 9000 名参与者中进行。在 3 年内的 5 个时间点比较了其中 1800 名个体的几何平均浓度(GMC)和血清转化率(SR)。在接种第一剂后 28 天,HA-L 和 HA-I 的 SR 分别为 98.08%(95%CI 95.59%-99.38%)和 99.64%(95%CI 98.93%-100.00%),在随后的 3 年内分别保持在 97.07%(95%CI 94.31%-98.73%)或更高和 96.73%(95%CI 94.07%-98.42%)或更高。HA-L 和 HA-I 组的 GMC 均表明,两种疫苗均能引起高抗-HAV 滴度,远高于人类免受 HAV 感染所需的保护阈值,且这些滴度持续存在。因此,HA-I 和 HA-L 疫苗均可提供出色的长期保护效果,支持这两种疫苗的常规使用。