HPV16/18 antibodies 16-years after single dose of bivalent HPV vaccination: Costa Rica HPV vaccine trial.

Carolina Porras, Byron Romero, Troy Kemp, Romain Fantin, Rolando Herrero, Allan Hildesheim, Rebeca Ocampo, Mónica S Sierra, Mitchell H Gail, John Schussler, John T Schiller, Douglas R Lowy, Ligia A Pinto, Danping Liu, Aimée R Kreimer
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Abstract

Background: The Costa Rica HPV Vaccine Trial provided initial evidence that 1 dose of the bivalent human papillomavirus (HPV) vaccine induces stabilizing antibody levels that may provide extended protection against HPV-16/18 infections. We report antibody seropositivity and stability 11 to 16 years after vaccination.

Methods: We invited a random subset of Costa Rica HPV Vaccine Trial participants (n = 398) who had received 3 doses and all women (n = 203) who had received 1 dose at 18 to 25 years of age to follow-up visits 11, 14, and 16 years after vaccination. We calculated HPV-16 and HPV-18 seropositivity and assessed change in enzyme-linked immunosorbent assay antibody levels 11 to 16 years after vaccination among 500 participants.

Results: By year 16, 99.4% (95% confidence interval [CI] = 96.8% to 100.0%) and 100.0% (95% CI = 98.9% to 100.0%) of 1-dose and 3-dose recipients, respectively, were HPV-16 seropositive and 98.8% (95% CI = 95.9% to 99.9%) and 100% (95% CI = 98.9% to 100.0%) of 1-dose and 3-dose recipients, respectively, were HPV-18 seropositive. Between years 11 and 16, women who had received 3 doses had a small but statistically significant decrease in the geometric mean concentration for HPV-16 of ‒12.4% (95% CI = ‒16.3% to ‒8.4%) and HPV-18 of ‒13.4% (95% CI = ‒17.2% to ‒9.4%). Among women who had received 1 dose, the decrease was statistically significant for HPV-16 at ‒8.9 (95% CI = ‒14.2% to ‒3.1%) but nonsignificant for HPV-18. Geometric mean concentration ratios of 3:1 dose (year 16) were 3.0 and 2.2 for HPV-16 and HPV-18, respectively.

Conclusions: HPV-16/18 seropositivity remained exceedingly high 16 years after vaccination. Over 5 years, small declines in antibodies were observed. Women should have protection for at least 20 years and likely much longer at the observed rate of decline.

单剂二价 HPV 疫苗接种 16 年后的 HPV16/18 抗体:哥斯达黎加 HPV 疫苗试验。
背景:哥斯达黎加 HPV 疫苗试验提供了初步证据,证明接种一剂二价人乳头瘤病毒 (HPV) 疫苗可诱导稳定的抗体水平,从而延长对 HPV-16/18 感染的保护。我们报告了接种疫苗 11 到 16 年后的抗体血清阳性率和稳定性:我们随机邀请了哥斯达黎加 HPV 疫苗试验参与者(n = 398)中接种过 3 次疫苗的人群和所有在 18-25 岁接种过 1 次疫苗的女性(n = 203)在接种疫苗后 11、14 和 16 年进行随访。我们计算了 500 名参与者在接种疫苗 11 至 16 年后的 HPV-16 和 HPV-18 血清阳性率,并评估了酶联免疫吸附试验抗体水平的变化:到第 16 年,1 剂和 3 剂接种者中分别有 99.4% (95% 置信区间 [CI] = 96.8% 到 100.0%)和 100.0%(95% CI = 98.9% 到 100.0%)的人乳头瘤病毒-16 血清阳性,1 剂和 3 剂接种者中分别有 98.8% (95% CI = 95.9% 到 99.9%)和 100% (95% CI = 98.9% 到 100.0%)的人乳头瘤病毒-18 血清阳性。在第11年至第16年期间,接受过3剂治疗的妇女的HPV-16几何平均浓度下降了-12.4%(95% CI = -16.3%至-8.4%)和HPV-18几何平均浓度下降了-13.4%(95% CI = -17.2%至-9.4%),降幅虽小,但具有统计学意义。在接受过1剂治疗的女性中,HPV-16的下降幅度为-8.9(95% CI = -14.2%至-3.1%),具有显著的统计学意义,但HPV-18的下降幅度并不显著。HPV-16和HPV-18的3:1剂量(第16年)几何平均浓度比分别为3.0和2.2:结论:接种疫苗 16 年后,HPV-16/18 血清阳性率仍然很高。结论:接种疫苗 16 年后,HPV-16/18 血清阳性率仍然很高。按照观察到的下降速度,妇女的保护期至少应为 20 年,甚至更长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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