Sustained efficacy and immunogenicity of the HPV-16/18 ASO4-adjuvanted vaccine up to 7.3 years in young adult women

被引:115
作者
De Carvalho, N. [1 ]
Teixeira, J. [2 ]
Roteli-Martins, C. M. [3 ]
Naud, P. [4 ]
De Borba, P. [5 ]
Zahaf, T. [6 ]
Sanchez, N. [7 ]
Schuind, A. [8 ]
机构
[1] Univ Fed Parana, Hosp Clin, Setor Infeccoes Ginecol & Obstet, BR-80430160 Curitiba, Parana, Brazil
[2] Univ Campinas UNICAMP, Ctr Atencao Integral Saude Mulher, Campinas, SP, Brazil
[3] Hosp Leonor Mendes de Barros, Secretaria Saude Sao Paulo, Sao Paulo, Brazil
[4] Univ Fed Rio Grande do Sul, Hosp Clin Porto Alegre, Porto Alegre, RS, Brazil
[5] Inst Prevencao Canc Ceara, Fortaleza, Ceara, Brazil
[6] GlaxoSmithKline Biol, Rixensart, Belgium
[7] GlaxoSmithKline Biol, Rio De Janeiro, Brazil
[8] GlaxoSmithKline Biol, King Of Prussia, PA USA
关键词
HPV-16/18; vaccine; Long-term efficacy; Cervical cancer; HUMAN-PAPILLOMAVIRUS TYPE-16; SUBSEQUENT HPV INFECTION; PARTICLE VACCINE; NEUTRALIZATION ASSAY; ANTIBODY-RESPONSE; NATURAL-HISTORY; LATIN-AMERICA; PREVALENCE; RISK; PERSISTENCE;
D O I
10.1016/j.vaccine.2010.07.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We report efficacy and immunogenicity of the HPV-16/18 ASO4-adjuvanted vaccine up to 7.3 years post-vaccination. The study was conducted in a population (N = 433) of women enrolled in Brazilian centres from an initial placebo-controlled study. Women were aged 15-25 years at first vaccination. During the most recent year of follow-up, approximately 7 years after initial vaccination, no cases of infection or cytohistological lesions associated with HPV-16/18 were observed in the vaccinees. Vaccine efficacy (95% confidence interval) up to 7.3 years was 94.5% (82.9, 98.9) for incident infection, 100% (55.7, 100) for 12-month persistent infection and 100% (-129.8, 100) for cervical intraepithelial neoplasia grade 2+. Antibody titres for total IgG and neutralising antibodies remained several folds above natural infection levels and >= 96% of women were seropositive. Vaccine safety was similar to placebo. This is the longest follow-up study for a licensed cervical cancer vaccine. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6247 / 6255
页数:9
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