Sevestre Julien, Hong Eva, Delbos Valérie, Terrade Aude, Mallet Eric, Deghmane Ala-Eddine, Lemée Ludovic, Taha Muhamed-Kheir, Caron François
Centre Hospitalier Universitaire, Rouen, France; Université de Rouen, France; Institut Pasteur, Paris, France.
Institut Pasteur, Paris, France.
Vaccine. 2017 Jul 13;35(32):4029-4033. doi: 10.1016/j.vaccine.2017.05.065. Epub 2017 Jun 16.
MenBvac® is an outer membrane vesicle (OMV)-based meningococcal vaccine. From 2006 to 2012, it was used to control a clonal B outbreak in Normandy (France). We aimed to analyse the durability of the response against the epidemic strain and coverage beyond the vaccine strain. These data should help to optimize the use of OMV-containing vaccines, such as the new 4CMenB/Bexsero® recombinant vaccine.
Serum bactericidal activity (SBA) was measured in two cohorts of children who received their first dose of MenBvac® at 1-5years of age and accepted to provide a blood sample either one or four years after a 2+1+1 schedule. All sera were tested against the outbreak strain. Sera from responder subjects were also tested against 12 additional B or C strains which were chosen to entirely, partially, or not at all match the two variable regions (VR1 and VR2) of the PorA vaccine strain.
Only 47.9% and 31.3% of subjects showed an SBA titre consistent with protection one and four years, respectively, after the last boost. Protective SBA titres were observed in all sera against B or C strains that entirely matched P1.7,16, and was high (75-100%) for all but one strain that partially matched VR1 or VR2. Extrapolating our data to the OMV component of 4CMenB/Bexsero® suggests that 14.5% of the current B strains would be covered based on PorA matching to the OMV component of 4CMenB/Bexsero® (regardless of the coverage of the three other vaccine components).
Our data confirm that OMV-based vaccines elicit short-lasting SBA titres and may require repeated booster injections. However, strain coverage may be greater than expected.
MenBvac®是一种基于外膜囊泡(OMV)的脑膜炎球菌疫苗。2006年至2012年期间,该疫苗被用于控制法国诺曼底地区的B群克隆菌株疫情。我们旨在分析针对流行菌株的免疫反应持久性以及疫苗菌株以外的覆盖率。这些数据应有助于优化含OMV疫苗(如新的4CMenB/Bexsero®重组疫苗)的使用。
在两组1至5岁首次接种MenBvac®且同意在2+1+1免疫程序后1年或4年提供血样的儿童中测量血清杀菌活性(SBA)。所有血清均针对疫情菌株进行检测。反应者的血清还针对另外12种B或C菌株进行检测,这些菌株被选择为与PorA疫苗菌株的两个可变区(VR1和VR2)完全、部分或完全不匹配。
在最后一次加强免疫后1年和4年,分别只有47.9%和31.3%的受试者显示出与保护作用一致的SBA滴度。在所有血清中均观察到针对完全匹配P1.7,16的B或C菌株的保护性SBA滴度,对于除一种部分匹配VR1或VR2的菌株外的所有菌株,该滴度高(75-100%)。将我们的数据外推至4CMenB/Bexsero®的OMV成分表明,基于与4CMenB/Bexsero®的OMV成分的PorA匹配,当前14.5%的B菌株将被覆盖(无论其他三种疫苗成分的覆盖率如何)。
我们的数据证实,基于OMV的疫苗引发的SBA滴度持续时间较短,可能需要重复加强注射。然而,菌株覆盖率可能高于预期。