Verstraeten Thomas, Descamps Dominique, David Marie-Pierre, Zahaf Toufik, Hardt Karin, Izurieta Patricia, Dubin Gary, Breuer Thomas
GlaxoSmithKline Biologicals, Rixensart, Belgium.
Vaccine. 2008 Dec 2;26(51):6630-8. doi: 10.1016/j.vaccine.2008.09.049.
Newly licensed vaccines against human papillomavirus (HPV) and hepatitis B (HBV), and several vaccines in development, including a vaccine against genital herpes simplex virus (HSV), contain a novel Adjuvant System, AS04, composed of 3-O-desacyl-4' monophosphoryl lipid A and aluminium salts. Given the background incidence of autoimmune disorders in some of the groups targeted for immunisation with these vaccines, it is likely that autoimmune events will be reported in temporal association with vaccination, even in the absence of a causal relationship. The objective of this integrated analysis was to assess safety of AS04 adjuvanted vaccines with regard to adverse events (AEs) of potential autoimmune aetiology, particularly in adolescents and young adults. All randomised, controlled trials of HPV-16/18, HSV and HBV vaccines were analysed in an integrated analysis of individual data (N = 68,512). A separate analysis of the HPV-16/18 vaccine trials alone was also undertaken (N = 39,160). All data were collected prospectively during the vaccine development programmes (mean follow-up of 21.4 months), and included in the analysis up to a pre-defined data lock point. Reporting rates of overall autoimmune events were around 0.5% and did not differ between the AS04 and control groups. The relative risk (AS04/control) of experiencing any autoimmune event was 0.98 (95% confidence intervals 0.80, 1.21) in the integrated analysis and 0.92 (0.70, 1.22) in the HPV-16/18 vaccine analysis. Relative risks calculated overall, for disease category or for individual events were close to 1, and all confidence intervals around the relative risk included 1, indicating no statistically significant difference in event rates between the AS04 and control groups. This integrated analysis of over 68,000 participants who received AS04 adjuvanted vaccines or controls demonstrated a low rate of autoimmune disorders, without evidence of an increase in relative risk associated with AS04 adjuvanted vaccines.
新获得许可的人乳头瘤病毒(HPV)和乙型肝炎(HBV)疫苗,以及几种正在研发的疫苗,包括一种抗生殖器单纯疱疹病毒(HSV)疫苗,都含有一种新型佐剂系统AS04,它由3-O-去酰基-4'-单磷酰脂质A和铝盐组成。鉴于在这些疫苗的部分目标免疫人群中自身免疫性疾病的背景发病率,即使不存在因果关系,也有可能在接种疫苗后短期内报告自身免疫事件。这项综合分析的目的是评估含AS04佐剂疫苗在潜在自身免疫病因导致的不良事件(AE)方面的安全性,尤其是在青少年和年轻人中。在一项个体数据综合分析中(N = 68,512)对所有HPV-16/18、HSV和HBV疫苗的随机对照试验进行了分析。还单独对HPV-16/18疫苗试验进行了分析(N = 39,160)。所有数据均在疫苗研发项目期间前瞻性收集(平均随访21.4个月),并纳入分析直至预定义的数据锁定点。总体自身免疫事件的报告率约为0.5%,AS04组和对照组之间无差异。在综合分析中,发生任何自身免疫事件的相对风险(AS04/对照组)为0.98(95%置信区间0.80, 1.21),在HPV-16/18疫苗分析中为0.92(0.70, 1.22)。总体、疾病类别或个体事件计算的相对风险接近1,相对风险周围的所有置信区间都包含1,表明AS04组和对照组之间事件发生率无统计学显著差异。这项对超过68,000名接受含AS04佐剂疫苗或对照的参与者的综合分析表明,自身免疫性疾病发生率较低,没有证据表明含AS04佐剂疫苗会增加相对风险。