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肠道病毒 71 型灭活疫苗的保护相关因素:免疫替代终点分析。

Correlates of protection for inactivated enterovirus 71 vaccine: the analysis of immunological surrogate endpoints.

机构信息

a Department of Public Health , Southeast University , Nanjing , China.

b Vaccine Clinical Trials Institute, Jiangsu Province Center for Disease Control and Prevention , Nanjing , China.

出版信息

Expert Rev Vaccines. 2017 Sep;16(9):945-949. doi: 10.1080/14760584.2017.1335603. Epub 2017 Jun 12.

DOI:10.1080/14760584.2017.1335603
PMID:28548626
Abstract

BACKGROUND

Inactivated Enterovirus 71 (EV71) vaccines showed significant efficacy against the diseases associated with EV71 and a neutralizing antibody (NTAb) titer of 1:16-1:32 was suggested as the correlates of the vaccine protection. This paper aims to further estimate the immunological surrogate endpoints for the protection of inactivated EV71 vaccines and the effect factors.

METHODS

Pre-vaccination NTAb against EV71 at baseline (day 0), post-vaccination NTAb against EV71 at day 56, and the occurrence of laboratory-confirmed EV71-associated diseases during a 24-months follow-up period were collected from a phase 3 efficacy trial of an inactivated EV71 vaccine. We used the mixed-scaled logit model and the absolute sigmoid function by some extensions in continuous models to estimate the immunological surrogate endpoint for the EV71 vaccine protection, respectively.

RESULTS

For children with a negative baseline of EV71 NTAb titers, an antibody level of 26.6 U/ml (1:30) was estimated to provide at least a 50% protection for 12 months, and an antibody level of 36.2 U/ml (1:42) may be needed to achieve a 50% protective level of the population for 24 months.

CONCLUSION

Both the pre-vaccination NTAb level and the vaccine protective period could affect the estimation of the immunological surrogate for EV71 vaccine. A post-vaccination NTAb titer of 1:42 or more may be needed for long-term protection.

CLINICAL TRIAL REGISTRATION

NCT01508247.

摘要

背景

灭活肠道病毒 71 型(EV71)疫苗对 EV71 相关疾病具有显著疗效,中和抗体(NTAb)滴度为 1:16-1:32 被认为是疫苗保护的相关指标。本研究旨在进一步评估灭活 EV71 疫苗的免疫替代终点及其影响因素。

方法

从一项灭活 EV71 疫苗的 3 期疗效试验中收集了基线(第 0 天)时针对 EV71 的预接种 NTAb、第 56 天时针对 EV71 的接种后 NTAb,以及 24 个月随访期间实验室确诊的 EV71 相关疾病的发生情况。我们分别使用混合比例对数模型和连续模型中的绝对 S 型函数的一些扩展来估计 EV71 疫苗保护的免疫替代终点。

结果

对于基线 EV71 NTAb 滴度为阴性的儿童,估计抗体水平为 26.6 U/ml(1:30)可提供至少 12 个月的 50%保护,而抗体水平为 36.2 U/ml(1:42)可能需要实现 24 个月的人群 50%保护水平。

结论

预接种 NTAb 水平和疫苗保护期都会影响对 EV71 疫苗免疫替代终点的估计。为了实现长期保护,可能需要接种后 NTAb 滴度达到 1:42 或更高。

临床试验注册

NCT01508247。

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