Division of Adolescent and Transition Medicine, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, MLC 4000, Cincinnati, OH 45229, United States.
Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30329, United States.
Vaccine. 2018 Feb 1;36(6):881-889. doi: 10.1016/j.vaccine.2017.12.042. Epub 2018 Jan 3.
The originally recommended dosing schedule, 0, 2, 6 months, for the 3-dose quadrivalent human papillomavirus vaccine (4vHPV) was often not followed, resulting in longer than recommended intervals between doses and interest in the effect of prolonged intervals. Recent two-dose recommendations require investigations into the effect of delaying dose 2.
This multi-site, prospective study enrolled healthy 9-17 year old girls (n = 1321) on the day of or within 28 days following a third dose of 4vHPV vaccination. Antibody titers to 4vHPV types were measured at one and six months post-dose 3 from all participants and post-dose 2 from participants who were on time for dose 3. To compare antibody responses, participants were categorized into groups: second and third doses on time (control group); on-time dose 2, substantially late dose 3 (group 2); substantially late dose 2, on-time dose 3 (group 3); both doses substantially late (group 4). Analyses compared age-adjusted geometric mean titers (GMTs) at one-month and six-months post-dose 3, effect of delaying the second dose, and two versus three doses as well as post-dose 2 GMTs, stratified by age.
Compared to on-time dosing, one-month post-dose 3 GMTs were non-inferior in groups 2, 3, and 4 and were superior in group 2. Six month post-dose 3 GMTs were superior in groups 2, 3, and 4 for each genotype, except HPV 18 in group 3. Age-adjusted post does 2 titers were significantly lower than post-dose 3 titers when dose 2 was on time but were significantly higher when dose 2 was substantially late. Participants ≥15 years old had no difference in post-dose 2 titers compared to <15 year olds when dose 2 was substantially delayed.
Prolonged intervals between doses do not appear to diminish and may enhance antibody response to 4vHPV. ClinicalTrials.gov (NCT00524745).
最初推荐的三剂四价人乳头瘤病毒(HPV)疫苗(4vHPV)接种时间表为 0、2、6 个月,但该时间表经常得不到遵守,导致各剂次之间的间隔时间长于推荐时间,人们对延长各剂次间隔时间的效果产生了兴趣。最近推荐的两剂次方案需要对推迟接种第二剂次的效果进行调查。
本多中心前瞻性研究纳入了 1321 名在接种完第三剂 4vHPV 疫苗当天或之后 28 天内的 9-17 岁健康女孩。所有参与者在接种第三剂后 1 个月和 6 个月时以及按时接种第三剂的参与者在接种第二剂后测量对 4vHPV 各型别的抗体滴度。为了比较抗体应答,将参与者分为以下几组:第二和第三剂次按时接种(对照组);按时接种第二剂次,第三剂次明显延迟(组 2);第三剂次按时接种,第二剂次明显延迟(组 3);两剂次均明显延迟(组 4)。分析比较了第三剂后 1 个月和 6 个月时的年龄调整几何平均滴度(GMT),延迟第二剂次的影响,以及两剂次和三剂次的效果,同时按年龄分层。
与按时接种相比,组 2、组 3 和组 4 在第三剂后 1 个月时的 GMT 非劣效,且组 2 的 GMT 更优。第三剂后 6 个月时,各基因型组 2、组 3 和组 4 的 GMT 均更优,除组 3 的 HPV18 外。当第二剂次按时接种时,其接种后 2 个月的滴度明显低于第三剂次,但当第二剂次明显延迟时,其滴度明显高于第三剂次。当第二剂次明显延迟时,≥15 岁的参与者的接种后 2 个月的滴度与<15 岁的参与者无差异。
各剂次之间的间隔时间延长似乎不会降低,并且可能增强对 4vHPV 的抗体应答。临床试验.gov(NCT00524745)。