Kaiser Permanente Vaccine Study Center, Oakland, CA 94612, USA.
Pediatr Infect Dis J. 2013 Jul;32(7):760-7. doi: 10.1097/INF.0b013e31828693c5.
The incidence of invasive meningococcal disease is highest in infants. A quadrivalent meningococcal serogroups A, C, W-135 and Y tetanus toxoid conjugate vaccine (MenACWY-TT) was evaluated in children 9-12 months of age.
We randomized infants (1:1) to receive 1 dose of MenACWY-TT at 12 months of age (ACWY-1 group) or 2 doses at 9 and 12 months (ACWY-2). We measured immunogenicity after each dose and 1 year after completing vaccination using human serum bactericidal antibody (hSBA) assays according to prespecified criteria of ≥ 1:8. Local and general symptoms were solicited for 8 days after vaccination. Adverse events were recorded for 6 months after the last dose.
We enrolled and vaccinated 349 subjects, of whom 248 reenrolled at Year 1 for evaluation of antibody persistence. Percentages of subjects with postvaccination hSBA ≥ 1:8 in the ACWY-1 group were 79.5%, 94.6%, 50.8% and 56.1% and in the 2-dose group (ACWY-2) were 88.4%, 100%, 99.3% and 99.3% postdose 2 for serogroups A, C, W-135 and Y, respectively. At Year 1, 80.0-99.1% in each group had hSBA ≥ 1:8, except for serogroup A, for which 20.6% (ACWY-1) and 25.9% (ACWY-2) retained hSBA ≥1:8. Both schedules were well-tolerated, with no observed increase in reactogenicity after the second dose.
MenACWY-TT was immunogenic when administered as a single dose at 12 months of age, or as 2 doses at 9 and 12 months, and had a clinically acceptable safety profile. Good antibody persistence was observed through 12 months postvaccination after both treatment schedules for serogroups C, W-135, Y.
侵袭性脑膜炎球菌病的发病率在婴儿中最高。一种四价脑膜炎球菌血清 A、C、W-135 和 Y 破伤风类毒素结合疫苗(MenACWY-TT)在 9-12 个月龄儿童中进行了评估。
我们将婴儿(1:1)随机分为两组,一组在 12 个月龄时接受 1 剂 MenACWY-TT(ACWY-1 组),另一组在 9 个月和 12 个月时接受 2 剂(ACWY-2 组)。我们根据预定的标准(≥1:8),在每次接种后以及接种后 1 年使用人血清杀菌抗体(hSBA)测定来测量免疫原性。接种后 8 天内,我们收集了局部和全身症状。接种最后一剂后,我们记录了 6 个月的不良事件。
我们共招募并接种了 349 名受试者,其中 248 名在第 1 年重新入组以评估抗体持久性。ACWY-1 组接种后 hSBA≥1:8 的受试者百分比分别为 79.5%、94.6%、50.8%和 56.1%,2 剂组(ACWY-2)分别为 88.4%、100%、99.3%和 99.3%。在第 1 年,每组中 80.0-99.1%的人 hSBA≥1:8,除了 A 组,20.6%(ACWY-1)和 25.9%(ACWY-2)保留 hSBA≥1:8。两种方案均具有良好的耐受性,第 2 剂接种后未见反应原性增加。
MenACWY-TT 在 12 个月龄时单剂接种或在 9 个月和 12 个月时接种 2 剂均具有免疫原性,且安全性可接受。两种治疗方案在接种后 12 个月时,C、W-135、Y 血清型的抗体持久性良好。