a Hospital del Niño "Dr. José Renán Esquivel", Infectious Disease Department, Panama City , Panama and distinguished investigator of the SNI (Senacyt, Panama).
b Centro de Atención e Investigación Médica Caimed. Bogotá , Colombia.
Hum Vaccin Immunother. 2018 May 4;14(5):1161-1174. doi: 10.1080/21645515.2018.1457595. Epub 2018 May 9.
This open-label, multicenter extension study (NCT02451514) assessed persistence of Neisseria meningitidis serogroups ABCWY antibodies 4 years after primary vaccination. Adolescents and young adults who previously received 2 doses of MenABCWY+OMV (Group III), 1 dose of MenACWY-CRM (Group VI), or newly-recruited vaccine-naïve participants (Group VII) were administered 1 (Group III) or 2 doses (Groups VI and VII) of MenABCWY+OMV, 1 month apart. Immunogenicity was assessed by human serum bactericidal assay (hSBA). Safety and reactogenicity were also evaluated. Percentages of participants with hSBA titers ≥8 (serogroups ACWY), ≥5 (serogroup B) and hSBA geometric mean titers (GMTs) were evaluated in all 129 enrolled participants (Group III: 33; Group VI: 46; Group VII: 50). Anti-ACWY antibody concentrations waned over 4 years post-vaccination, but remained above pre-vaccination concentrations. Similarly, levels of antibodies against serogroup B test strains also waned over 4 years post-vaccination, but remained above pre-vaccination concentrations for some strains. MenABCWY+OMV booster induced a robust anamnestic anti-ACWY response in Group III and VI and a good response against serogroup B test strains (≥82%) in Group III. In serogroup B-naïve participants (Groups VI and VII), anti-B responses to 2 doses of MenABCWY+OMV were less homogenous and lower than in Group III. MenABCWY+OMV was reactogenic, but well-tolerated. No safety concerns were identified. These findings indicate that although antibodies against N. meningitidis serogroups ABCWY waned over 4 years post-vaccination, exposure to a MenABCWY+OMV booster dose elicits an anamnestic response in adolescents previously exposed to the same or another multivalent meningococcal vaccine.
本开放性、多中心扩展研究(NCT024514)评估了初次接种后 4 年内脑膜炎奈瑟菌血清型 ABCWY 抗体的持久性。先前接受过 2 剂 MenABCWY+OMV(III 组)、1 剂 MenACWY-CRM(VI 组)或新招募的疫苗初免参与者(VII 组)的青少年和年轻成年人,分别接受了 1(III 组)或 2 剂(VI 和 VII 组)MenABCWY+OMV,间隔 1 个月。通过人血清杀菌试验(hSBA)评估免疫原性。还评估了安全性和反应原性。所有 129 名入组参与者(III 组:33 名;VI 组:46 名;VII 组:50 名)的 hSBA 滴度≥8(血清型 ACWY)、≥5(血清型 B)和 hSBA 几何平均滴度(GMT)的参与者百分比进行了评估。接种疫苗 4 年后,抗-ACWY 抗体浓度逐渐下降,但仍高于接种前的浓度。类似地,针对脑膜炎奈瑟菌 B 血清型测试株的抗体水平也在接种疫苗后 4 年内逐渐下降,但对于一些菌株仍高于接种前的浓度。在 III 组和 VI 组中,MenABCWY+OMV 加强剂诱导了针对 ACWY 的强烈回忆性反应,而在 III 组中,针对 B 血清型测试菌株的反应良好(≥82%)。在 B 血清型初免参与者(VI 和 VII 组)中,MenABCWY+OMV 两剂接种的 B 反应不如 III 组均匀且较低。MenABCWY+OMV 具有反应原性,但耐受性良好。未发现安全性问题。这些发现表明,尽管接种疫苗后 4 年内针对脑膜炎奈瑟菌血清型 ABCWY 的抗体逐渐下降,但暴露于 MenABCWY+OMV 加强剂量可在先前接触过相同或另一种多价脑膜炎球菌疫苗的青少年中引发回忆反应。