A phase I study to evaluate a human papillomavirus (HPV) type 18 L1 VLP vaccine

被引:78
作者
Ault, KA
Giuliano, AR
Edwards, RP
Tamms, G
Kim, LL
Smith, JF
Jansen, KU
Allende, M
Taddeo, FJ
Skulsky, DM
Barr, E
机构
[1] Univ Iowa Hosp & Clin, Dept Obstet & Gynecol, Iowa City, IA 52242 USA
[2] Univ Arizona, Arizona Canc Ctr, Tucson, AZ USA
[3] Univ Pittsburgh, Dept Obstet Gynecol & Reprod Sci, Pittsburgh, PA USA
[4] Merck & Co Inc, Merck Res Labs, W Point, PA USA
关键词
human papilloma virus; vaccination; serology;
D O I
10.1016/j.vaccine.2004.02.020
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human papillomavirus (HPV) infection can cause genital warts and cervical cancer. HPV types 6 and 11 cause >90% of genital wart cases; HPV16 and 18 cause 70% of cervical cancers. A prophylactic HPV (types 6, 11, 16, 18) L1 virus-like particle (VLP) vaccine may substantially reduce the incidence of these lesions. This report describes the results of a phase I study of the HPV18 component of such a vaccine. Forty women were randomized to receive either HPV18 L1 VLP vaccine or placebo. Anti-HPV18 responses were measured using a competitive radioimmunoassay (cRIA). Tolerability was evaluated using vaccination report cards (VRC). The study showed that the HPV18 L1 VLP vaccine was generally well-tolerated and highly immunogenic. Peak anti-HPV18 geometric mean titers (GMT) in vaccines were 60-fold greater than those observed in women following natural HPV18 infection. Further studies of a multivalent HPV L I VLP vaccines are warranted. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3004 / 3007
页数:4
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