Haney Douglas J, Lock Michael D, Simon Jakub K, Harris Jason, Gurwith Marc
PaxVax, Inc., Redwood City, CA
PaxVax, Inc., Redwood City, CA.
Clin Vaccine Immunol. 2017 May 31;24(8). doi: 10.1128/CVI.00098-17.
Immunologic correlates of protection can be used to infer vaccine efficacy for populations in which challenge trials or field studies are infeasible. In a recent cholera challenge trial (WH Cohen et al, Clinical Infectious Disease 62: 1329-1335, 2016), 134 North American cholera-naïve volunteers were randomized to receive either the live, attenuated single-dose cholera vaccine CVD 103-HgR or placebo, and titers of vibriocidal antibodies against classical Inaba were assessed 10 days after treatment. Subsequent to the immunologic evaluation, each subject ingested a fixed quantity of virulent O1 El Tor Inaba. Data from this trial suggest that vaccine-induced increase in vibriocidal antibody titer prior to challenge is tightly linked with protection: 51/51 vaccinees with post-vaccination vibriocidal titers >= 2560 were protected against moderate/severe cholera, and 60/62 vaccinees who seroconverted, or experienced a 4-fold or greater increase in vibriocidal titer relative to pre-vaccination levels, were similarly protected. Atypically high vibriocidal titers were observed in some placebo subjects; protection was limited in these individuals and differed substantially from the level of protection experienced by vaccinees with the same post-vaccination titers. Since only 1 of 66 placebo recipients experienced seroconversion, seroconversion was found to be uniquely associated with vaccination and insensitive to the effects of factors that can cause titers to be elevated but are weakly associated with protection. Thus, vibriocidal seroconversion was found to be better than vibriocidal titer for inferring vaccine efficacy in cholera-naïve populations for which studies based upon exposure to are impractical.
对于那些无法进行攻毒试验或现场研究的人群,保护的免疫相关指标可用于推断疫苗效力。在最近一项霍乱攻毒试验(WH·科恩等人,《临床传染病》62: 1329 - 1335, 2016)中,134名未接触过霍乱的北美志愿者被随机分组,分别接受单剂量减毒活霍乱疫苗CVD 103-HgR或安慰剂,并在治疗10天后评估针对古典伊纳型霍乱弧菌的杀菌抗体滴度。免疫评估之后,每个受试者摄入固定量的有毒O1埃尔托伊纳型霍乱弧菌。该试验数据表明,攻毒前疫苗诱导的杀菌抗体滴度升高与保护密切相关:接种疫苗后杀菌滴度≥2560的51/51名接种者免受中度/重度霍乱感染,60/62名发生血清转化或杀菌滴度相对于接种前水平升高4倍或更高的接种者也得到了类似保护。在一些安慰剂受试者中观察到异常高的杀菌滴度;这些个体的保护作用有限,与相同接种后滴度的接种者所经历的保护水平有很大差异。由于66名安慰剂接受者中只有1人发生血清转化,因此发现血清转化与接种疫苗具有独特关联,并且对那些可导致滴度升高但与保护作用弱相关的因素的影响不敏感。因此,对于未接触过霍乱且基于暴露进行研究不切实际的人群,发现杀菌血清转化比杀菌滴度更能准确推断疫苗效力。