Bissett Sara L, Godi Anna, Jit Mark, Beddows Simon
Virus Reference Department, Public Health England, London, UK.
Modelling and Economics Unit, Public Health England, London, UK; Department of Infectious Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, UK.
Vaccine. 2017 Jul 13;35(32):3922-3929. doi: 10.1016/j.vaccine.2017.06.028. Epub 2017 Jun 17.
Human papillomavirus vaccines have demonstrated remarkable efficacy against persistent infection and disease associated with vaccine-incorporated genotypes and a degree of efficacy against some genetically related, non-vaccine-incorporated genotypes. The vaccines differ in the extent of cross-protection against these non-vaccine genotypes. Data supporting the role for neutralizing antibodies as a correlate or surrogate of cross-protection are lacking, as is a robust assessment of the seroconversion rates against these non-vaccine genotypes.
We performed a systematic review and meta-analysis of available data on vaccine-induced neutralizing antibody seropositivity to non-vaccine incorporated HPV genotypes.
Of 304 articles screened, 9 were included in the analysis representing ca. 700 individuals. The pooled estimate for seropositivity against HPV31 for the bivalent vaccine (86%; 95%CI 78-91%) was higher than that for the quadrivalent vaccine (61%; 39-79%; p=0.011). The pooled estimate for seropositivity against HPV45 for the bivalent vaccine (50%; 37-64%) was also higher than that for the quadrivalent vaccine (16%; 6-36%; p=0.007). Seropositivity against HPV33, HPV52 and HPV58 were similar between the vaccines. Mean seropositivity rates across non-vaccine genotypes were positively associated with the corresponding vaccine efficacy data reported from vaccine trials.
These data improve our understanding of vaccine-induced functional antibody specificity against non-vaccine incorporated genotypes and may help to parameterize vaccine-impact models and improve patient management in a post-vaccine setting.
人乳头瘤病毒疫苗已证明对与疫苗所含基因型相关的持续感染和疾病具有显著疗效,并且对一些基因相关的非疫苗所含基因型也有一定疗效。这些疫苗在针对这些非疫苗基因型的交叉保护程度上存在差异。目前缺乏支持中和抗体作为交叉保护的相关指标或替代指标作用的数据,也缺乏对针对这些非疫苗基因型的血清转化率的有力评估。
我们对关于疫苗诱导的针对非疫苗所含人乳头瘤病毒基因型的中和抗体血清阳性的现有数据进行了系统评价和荟萃分析。
在筛选的304篇文章中,9篇被纳入分析,涉及约700名个体。二价疫苗针对HPV31的血清阳性合并估计值(86%;95%CI 78 - 91%)高于四价疫苗(61%;39 - 79%;p = 0.011)。二价疫苗针对HPV45的血清阳性合并估计值(50%;37 - 64%)也高于四价疫苗(16%;6 - 36%;p = 0.007)。两种疫苗针对HPV33、HPV52和HPV58的血清阳性率相似。非疫苗基因型的平均血清阳性率与疫苗试验报告的相应疫苗疗效数据呈正相关。
这些数据增进了我们对疫苗诱导的针对非疫苗所含基因型的功能性抗体特异性的理解,可能有助于对疫苗影响模型进行参数化,并改善疫苗接种后环境下的患者管理。