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两种实验性A群、C群、W群和Y群脑膜炎球菌疫苗制剂的比较评估:一项2期随机对照试验的结果

A comparative evaluation of two investigational meningococcal ABCWY vaccine formulations: Results of a phase 2 randomized, controlled trial.

作者信息

Block Stan L, Szenborn Leszek, Daly Wendy, Jackowska Teresa, D'Agostino Diego, Han Linda, Dull Peter M, Smolenov Igor

机构信息

Kentucky Pediatric and Adult Research, Bardstown, KY, USA.

Department of Pediatric Infectious Diseases, Wroclaw Medical University, Wroclaw, Poland.

出版信息

Vaccine. 2015 May 15;33(21):2500-10. doi: 10.1016/j.vaccine.2015.03.001. Epub 2015 Mar 17.

Abstract

BACKGROUND

A meningococcal vaccine protective against all major disease-associated serogroups (A, B, C, W and Y) is an unmet public health need. In this phase 2 observer-blinded, randomized, controlled study, two investigational meningococcal ABCWY vaccine formulations were evaluated to assess their immunological noninferiority to a licensed quadrivalent meningococcal ACWY glycoconjugate vaccine (MenACWY-CRM) for serogroups ACWY and immunogenicity against serogroup B test strains, as well as for formulation selection based on a desirability index (DI). Each investigational MenABCWY formulation contained recombinant protein and outer membrane vesicle (OMV) components of a licensed serogroup B vaccine (4CMenB) combined with components of MenACWY-CRM.

METHODS

A total of 484 healthy 10-25 year-old participants were randomized to receive two doses, two months apart, of an investigational MenABCWY formulation that contained either a full or one-quarter dose of OMV, 4CMenB alone, or a Placebo followed by MenACWY-CRM. Immunogenicity against each of serogroups ACWY and four serogroup B test strains was assessed by serum bactericidal assay with human complement (hSBA). MenABCWY formulations were compared by a DI based on key immunogenicity and reactogenicity parameters.

RESULTS

Seroresponse rates for serogroups ACWY were significantly higher after two doses of either MenABCWY formulation than after one dose of MenACWY-CRM: respectively, A: 90-92% vs. 73%; C: 93-95% vs. 63%; W: 80-84% vs. 65%; and Y: 90-92% vs. 75%. Prespecified noninferiority criteria were met. Both MenABCWY formulations induced substantial immune responses against serogroup B test strains, although 4CMenB responses were higher. Overall DIs for both MenABCWY formulations were similar. Reactogenicity profiles of the MenABCWY formulations were similar to each other and to that of 4CMenB. No vaccine-related serious adverse events were reported.

CONCLUSIONS

Both investigational MenABCWY formulations elicited robust immune responses against serogroups ACWY and serogroup B test strains, and had acceptable reactogenicity profiles, with no safety concerns identified.

摘要

背景

一种能预防所有主要疾病相关血清群(A、B、C、W和Y)的脑膜炎球菌疫苗是一项尚未满足的公共卫生需求。在这项2期观察者盲法、随机、对照研究中,对两种研究性脑膜炎球菌ABCWY疫苗制剂进行了评估,以评估它们在血清群ACWY方面相对于已获许可的四价脑膜炎球菌ACWY糖结合疫苗(MenACWY-CRM)的免疫非劣效性,以及对血清群B测试菌株的免疫原性,并根据合意性指数(DI)进行制剂选择。每种研究性MenABCWY制剂都包含一种已获许可的血清群B疫苗(4CMenB)的重组蛋白和外膜囊泡(OMV)成分,以及MenACWY-CRM的成分。

方法

总共484名10 - 25岁的健康参与者被随机分配,间隔两个月接受两剂研究性MenABCWY制剂,其中一种制剂含有全剂量或四分之一剂量的OMV,单独使用4CMenB,或使用安慰剂后再接种MenACWY-CRM。通过用人补体的血清杀菌试验(hSBA)评估针对血清群ACWY和四种血清群B测试菌株的免疫原性。根据关键免疫原性和反应原性参数,通过DI对MenABCWY制剂进行比较。

结果

两剂任一种MenABCWY制剂后血清群ACWY的血清反应率显著高于一剂MenACWY-CRM后的反应率:分别为,A群:90 - 92%对73%;C群:93 - 95%对63%;W群:80 - 84%对65%;Y群:90 - 92%对75%。达到了预先设定的非劣效性标准。两种MenABCWY制剂都诱导了针对血清群B测试菌株的显著免疫反应,尽管4CMenB的反应更高。两种MenABCWY制剂的总体DI相似。MenABCWY制剂的反应原性特征彼此相似,且与4CMenB的相似。未报告与疫苗相关的严重不良事件。

结论

两种研究性MenABCWY制剂都引发了针对血清群ACWY和血清群B测试菌株的强烈免疫反应,且具有可接受的反应原性特征,未发现安全问题。

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