Insituto Hispalense de Pediatría, Sevilla, Spain.
Vaccine. 2010 Aug 16;28(36):5837-44. doi: 10.1016/j.vaccine.2010.06.065. Epub 2010 Jun 29.
We report on the evaluation of the immunogenicity and reactogenicity/safety of AS03-adjuvanted vaccine against pandemic influenza A/H1N1/2009 in young children. In this open-label, randomized study, 157 healthy children aged 6-35 months received two doses (21 days apart) of split-virion inactivated A/California/7/2009 H1N1 vaccine containing either (i) 1.9microg hemagglutinin (HA) and AS03(B) (5.93mg tocopherol) (N=104) or (ii) 3.75mug HA and AS03(A) (11.86mg tocopherol) (N=53). At 21 days following the first dose of AS03(B)-adjuvanted vaccine (1.9microg HA) the percentage of children with hemagglutination-inhibition titers of >or=40 against the vaccine strain rose from 3.0% before vaccination to 100%. The seroconversion rate was 99% and the geometric mean titer (GMT) increased from 6 to 313. After the second dose the GMT increased further to 2008. The higher dose AS03(A)-adjuvanted 3.75microg HA vaccine did not further increase the immune response. Solicited symptoms reported within 7 days following vaccination were mainly mild to moderate. After the first dose of AS03(B)-adjuvanted vaccine (1.9microg HA) the most common solicited symptoms were pain at the injection site (35.6%) and irritability (31.7%). Fever (axillary >or=37.5 degrees C) was reported with an incidence of 20.2%. After the second dose reactogenicity tended to increase (injection site pain: 41.3%; irritability: 46.2%; fever >or=37.5 degrees C: 67.3%). Spontaneously reported adverse events with an intensity that prevented normal activities were documented for 2.9-6.7% of doses with only one event (vomiting) considered related to vaccination. There was one serious adverse event reported in the AS03(A)-adjuvanted 3.75microg HA vaccine group (traumatic brain injury) which was not considered as related to vaccination. In conclusion, these data suggest that a first dose of AS03(B)-adjuvanted A/H1N1/2009 vaccine containing 1.9microg HA in children 6-35 months old is highly immunogenic and that the overall reactogenicity profile is acceptable although reactions including fever tend to increase after a second dose.
我们报告了评估 AS03 佐剂的流感大流行疫苗对 6-35 月龄幼儿的免疫原性和反应原性/安全性。在这项开放性、随机研究中,157 名健康的 6-35 月龄儿童接受了两剂(间隔 21 天)裂解病毒灭活 A/加利福尼亚/7/2009 H1N1 疫苗,其中(i)含有 1.9μg 血凝素(HA)和 AS03(B)(5.93mg 生育酚)(n=104)或(ii)含有 3.75μg HA 和 AS03(A)(11.86mg 生育酚)(n=53)。在接种第一剂 AS03(B)-佐剂疫苗(1.9μg HA)后 21 天,对疫苗株血凝抑制滴度大于或等于 40 的儿童百分比从接种前的 3.0%上升至 100%。血清转化率为 99%,几何平均滴度(GMT)从 6 增加到 313。接种第二剂后,GMT 进一步增加到 2008。较高剂量的 AS03(A)-佐剂 3.75μg HA 疫苗并未进一步增加免疫反应。接种后 7 天内报告的应征症状主要为轻度至中度。接种第一剂 AS03(B)-佐剂疫苗(1.9μg HA)后,最常见的应征症状是注射部位疼痛(35.6%)和烦躁(31.7%)。发热(腋温>或=37.5°C)的报告发生率为 20.2%。接种第二剂后,反应性趋于增加(注射部位疼痛:41.3%;烦躁:46.2%;腋温>或=37.5°C:67.3%)。以预防正常活动的强度记录到的自发报告不良事件占剂量的 2.9-6.7%,仅有 1 例事件(呕吐)被认为与接种有关。在接种 AS03(A)-佐剂 3.75μg HA 疫苗的组中报告了 1 例严重不良事件(创伤性脑损伤),认为与接种无关。总之,这些数据表明,6-35 月龄儿童接种一剂含 1.9μg HA 的 AS03(B)-佐剂 A/H1N1/2009 疫苗具有高度的免疫原性,尽管接种第二剂后反应包括发热的发生率趋于增加,但总体反应原性特征是可以接受的。