Bermal Nancy, Huang Li-Min, Dubey A P, Jain Hermant, Bavdekar Ashish, Lin Tzou-Yien, Bianco Veronique, Baine Yaela, Miller Jacqueline M
Research Institute for Tropical Medicine, Filinvest Corporate City, Alabang, Muntinlupa City, Philippines.
Hum Vaccin. 2011 Feb;7(2):239-47. doi: 10.4161/hv.7.2.14068. Epub 2011 Feb 1.
The highest incidence of invasive meningococcal disease is in young children, with a second peak in adolescents/young adults. All five major disease-causing serogroups (A, B, C, W-135 and Y) have been described in Asia. Immunogenicity and safety of the investigational meningococcal ACWY-tetanus toxoid conjugate vaccine (ACWY-TT, GlaxoSmithKline Biologicals) was evaluated in healthy, meningococcal conjugate vaccine-naïve adolescents in the Philippines, India and Taiwan. 1025 adolescents were randomized (3:1) to receive one dose of ACWY-TT or tetravalent ACWY polysaccharide vaccine (Mencevax™, Men-PS). Serum bactericidal activity using rabbit complement (rSBA) was measured. Local and systemic adverse reactions were recorded for 4 days. Safety data were pooled with results from a second, similarly designed study in adults for evaluation of grade 3 systemic events. The pre-specified immunogenicity criterion for non-inferiority to Men-PS was met. One month post-vaccination, ≥85.4%-97.1% had a vaccine response (post-titre ≥1:8 in initially seronegative and ≥4-fold increase in seropositive), versus 78.0%-96.6% after Men-PS, against each vaccine serogroup. Exploratory comparisons showed statistically significantly higher post-vaccination rSBA geometric mean titres against all serogroups following ACWY-TT versus Men-PS. Exploratory analysis showed no statistically significant differences between groups in grade 3 general symptoms; however, the statistical criterion for non-inferiority between pooled treatment groups in terms of the ratio of incidences of grade 3 general symptoms was not demonstrated. No SAEs were related to vaccination. ACWY-TT was immunogenic in Asian adolescents with a reactogenicity profile that was clinically acceptable and similar to that of licensed Men-PS. The results of this study indicate that ACWY-TT could be used as a third conjugate vaccine in the protection of adolescents against meningococcal disease.
侵袭性脑膜炎球菌病的发病率最高的是幼儿,在青少年/年轻成年人中出现第二个高峰。亚洲已发现所有五个主要致病血清群(A、B、C、W-135和Y)。在菲律宾、印度和台湾的健康、未接种过脑膜炎球菌结合疫苗的青少年中评估了研究性脑膜炎球菌ACWY-破伤风类毒素结合疫苗(ACWY-TT,葛兰素史克生物制品公司)的免疫原性和安全性。1025名青少年被随机分组(3:1)接受一剂ACWY-TT或四价ACWY多糖疫苗(Mencevax™,Men-PS)。使用兔补体(rSBA)测量血清杀菌活性。记录4天的局部和全身不良反应。将安全性数据与另一项针对成年人的类似设计研究的结果合并,以评估3级全身事件。达到了非劣于Men-PS的预先设定的免疫原性标准。接种疫苗后一个月,相对于Men-PS接种后78.0%-96.6%的比例,针对每个疫苗血清群,≥85.4%-97.1%的人有疫苗反应(初始血清阴性者接种后滴度≥1:8,血清阳性者滴度增加≥4倍)。探索性比较显示,接种疫苗后,ACWY-TT组针对所有血清群的rSBA几何平均滴度在统计学上显著高于Men-PS组。探索性分析显示,两组在3级一般症状方面无统计学显著差异;然而,未证明合并治疗组在3级一般症状发生率比值方面的非劣效性统计标准。没有严重不良事件与疫苗接种相关。ACWY-TT在亚洲青少年中具有免疫原性,其反应原性特征在临床上是可接受的,且与已获许可的Men-PS相似。这项研究结果表明ACWY-TT可作为第三种结合疫苗用于保护青少年预防脑膜炎球菌病。