Watson-Jones Deborah, Changalucha John, Maxwell Caroline, Whitworth Hilary, Mutani Paul, Kemp Troy J, Kamala Beatrice, Indangasi Jackton, Constantine George, Hashim Ramadhan, Mwanzalima David, Wiggins Rebecca, Mmbando Devis, Connor Nicholas, Pavon Miquel A, Lowe Brett, Kapiga Saidi, Mayaud Philippe, de Sanjosé Silvia, Dillner Joakim, Hayes Richard J, Lacey Charles J, Pinto Ligia, Baisley Kathy
Mwanza Intervention Trials Unit, National Institute for Medical Research, Mwanza, Tanzania; Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Mwanza Intervention Trials Unit, National Institute for Medical Research, Mwanza, Tanzania.
Lancet Glob Health. 2025 Feb;13(2):e319-e328. doi: 10.1016/S2214-109X(24)00477-7.
WHO has recommended that one dose of human papillomavirus (HPV) vaccine can be given to individuals aged 9-20 years to prevent HPV infection. Estimating durability of immune responses after a single dose in the target age for vaccination is important. We report immunogenicity results in Tanzanian girls up to 5 years after receiving a dose.
In this open-label, randomised controlled trial (the Dose Reduction Immunobridging and Safety Study of Two HPV Vaccines in Tanzanian Girls [DoRIS] trial), 930 Tanzanian schoolgirls aged 9-14 years were enrolled and randomly allocated to receive one, two, or three doses of either the two-valent vaccine (Cervarix; GSK, Wavre, Belgium) or nine-valent vaccine (Gardasil-9; Merck Sharp & Dohme, Haarlem, Netherlands). Seropositivity specific to HPV16 or HPV18, antibody geometric mean concentrations (GMCs), and antibody avidity were measured annually up to month 36. Participants in the one-dose and two-dose groups were followed annually in a long-term extension of the DoRIS trial to month 60; the primary outcome was seropositivity specific to HPV16 or HPV18 comparing one dose with two doses.
Single-dose seropositivity for HPV16 IgG antibodies at month 60 with either vaccine was more than 99% and non-inferior to two doses. 98% of girls in the one-dose two-valent vaccine group and 93% in the one-dose nine-valent group were seropositive for HPV18 at month 60; however, the non-inferiority criteria for HPV18 seropositivity comparing one dose with two doses were not met. Although HPV16 and HPV18 antibody GMCs after one dose were lower than those observed after two doses, antibody GMCs in the one-dose groups remained stable from month 12 to month 60. There was no evidence of a difference between the one-dose and two-dose groups in HPV16 or HPV18 antibody avidity at month 36 for either vaccine.
A single dose of HPV vaccine in girls aged 9-14 years continues to provide stable immune responses 5 years after vaccination, although ongoing surveillance for potential waning immunity after a single dose is needed. Participants are being followed up to 9 years after vaccination.
UK Department of Health and Social Care, UK Foreign, Commonwealth & Development Office, Global Challenges Research Fund, UK Medical Research Council, and the Wellcome Trust through the Joint Global Health Trials Scheme; Bill & Melinda Gates Foundation.
世界卫生组织建议,9至20岁的人群可接种一剂人乳头瘤病毒(HPV)疫苗以预防HPV感染。评估在目标接种年龄接种一剂疫苗后免疫反应的持久性很重要。我们报告了坦桑尼亚女孩接种一剂疫苗后长达5年的免疫原性结果。
在这项开放标签、随机对照试验(坦桑尼亚女孩两种HPV疫苗的剂量减少免疫桥接和安全性研究[DoRIS]试验)中,招募了930名9至14岁的坦桑尼亚女学生,并将她们随机分配接受一剂、两剂或三剂二价疫苗(希瑞适;葛兰素史克公司,比利时瓦夫尔)或九价疫苗(佳达修9;默克雪兰诺公司,荷兰哈勒姆)。在36个月前每年测量HPV16或HPV18特异性血清阳性率、抗体几何平均浓度(GMC)和抗体亲和力。在DoRIS试验的长期扩展研究中,对单剂组和两剂组的参与者进行了长达60个月的年度随访;主要结局是比较单剂与两剂HPV16或HPV18特异性血清阳性率。
接种任一疫苗后60个月时,HPV16 IgG抗体的单剂血清阳性率均超过99%,且不低于两剂。单剂二价疫苗组98%的女孩和单剂九价疫苗组93%的女孩在60个月时HPV18血清阳性;然而,单剂与两剂HPV18血清阳性率的非劣效性标准未达到。虽然单剂后的HPV16和HPV18抗体GMC低于两剂后的水平,但单剂组的抗体GMC从第12个月到第60个月保持稳定。对于任一疫苗,在36个月时,单剂组和两剂组在HPV16或HPV18抗体亲和力方面均无差异证据。
9至14岁女孩接种一剂HPV疫苗后,在接种后5年仍能持续提供稳定的免疫反应,不过仍需对单剂疫苗后潜在的免疫减弱进行持续监测。参与者在接种后将被随访至9年。
英国卫生和社会保健部、英国外交、联邦及发展办公室、全球挑战研究基金、英国医学研究理事会以及惠康信托基金会通过联合全球健康试验计划提供资助;比尔及梅琳达·盖茨基金会。