Secor Andrew M, Driver Matthew, Kharono Brenda, Hergott Dianna, Liu Gui, Barnabas Ruanne V, Dull Peter, Hawes Stephen E, Drain Paul K
START Center, University of Washington, Seattle, WA 98195, USA.
Department of Global Health, University of Washington, Seattle, WA 98195, USA.
Vaccines (Basel). 2020 Oct 20;8(4):618. doi: 10.3390/vaccines8040618.
Alternative dosing schedules for licensed human papilloma virus (HPV) vaccines, particularly single dose and extended intervals between doses (>12 months), are being considered to address vaccine shortages and improve operational flexibility. We searched PUBMED/MEDLINE for publications reporting immunogenicity data following administration of one of the licensed HPV vaccines (2vHPV, 4vHPV, and 9vHPV) to females aged 9-26 years. We conducted non-inferiority analyses comparing alternative to standard schedules using mixed effects meta-regression controlling for baseline HPV status and disaggregated by vaccine, subtype, time point, and age group (9-14 and 15-26 years). Non-inferiority was defined as the lower bound of the 95% confidence interval (CI) for the geometric mean titer (GMT) ratio being greater than 0.5. Our search returned 2464 studies, of which 23 were included in data analyses. When evaluated against standard schedules, although robust immunogenicity was demonstrated across all multi-dose groups, non-inferiority of extended interval dosing was mixed across vaccines, subtypes, and time points. Single dose did not meet the criteria for non-inferiority in any comparisons. Sparse data limited the number of possible comparisons, and further research is warranted.
正在考虑对已获许可的人乳头瘤病毒(HPV)疫苗采用替代给药方案,尤其是单剂量和延长剂次间隔时间(>12个月),以应对疫苗短缺问题并提高操作灵活性。我们在PUBMED/MEDLINE中检索了相关出版物,这些出版物报告了对9至26岁女性接种一种已获许可的HPV疫苗(2价HPV、4价HPV和9价HPV)后的免疫原性数据。我们使用混合效应元回归进行非劣效性分析,比较替代方案与标准方案,同时控制基线HPV状态,并按疫苗、亚型、时间点和年龄组(9至14岁和15至26岁)进行分类。非劣效性定义为几何平均滴度(GMT)比值的95%置信区间(CI)下限大于0.5。我们的检索共返回2464项研究,其中23项纳入数据分析。与标准方案相比,尽管所有多剂次组均显示出强大的免疫原性,但延长剂次间隔给药的非劣效性在不同疫苗、亚型和时间点存在差异。单剂量在任何比较中均未达到非劣效性标准。数据稀少限制了可能的比较数量,因此有必要开展进一步研究。