单剂量 HPV 疫苗接种对感染和未感染 HIV 的南非少女中 HPV 16 和 18 流行率的影响。

Sinead Delany-Moretlwe, Dorothy A Machalek, Danielle Travill, Kathy Petoumenos, Dorothy C Nyemba, Zizipho Z A Mbulawa, Nontokozo Ndlovu, John M Kaldor, Helen Rees
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引用次数: 0

摘要

背景:世界卫生组织已经批准了单剂量人类乳头瘤病毒(HPV)疫苗接种,但在艾滋病高负担地区,有关其对 HPV 感染率影响的数据十分有限:方法:在南非的一个地区开展了一项以学校为基础的活动,为 10 年级的少女接种了一剂二价 HPV 疫苗。通过重复横断面调查评估了对 HPV 16 和 18 流行率的影响。2019 年,在接种疫苗前人群(n = 506,包括 157 名艾滋病病毒感染者)中对 17-18 岁女孩进行的诊所调查确定了 HPV 16 和 18 的流行率;2021 年,在同一年龄组和地点对符合单剂量接种条件的人群(n = 892,包括 117 名艾滋病病毒感染者)进行了重复调查。使用 Seegene Anyplex II HPV 28 在自取的阴道拭子上检测 HPV DNA。使用根据不同调查之间性行为差异调整后的流行率估算了总体人口影响和不同艾滋病毒感染状况的人口影响:在该地区符合条件的高中女生(n = 66)中,单剂量疫苗接种活动的覆盖率为 72%(6673 名中的 4807 名)。在疫苗接种后的调查中,HPV 16 和 18 感染率总体降低了 35%(调整后感染率比值 = 0.65,95% 置信区间 [CI] = 0.51 至 0.83;P < .001),HIV 感染者的感染率降低了 37%(调整后感染率比值 = 0.63,95% 置信区间 = 0.41 至 0.95;P = .026)。非疫苗致癌 HPV 类型 33、35、39、51、52、56、58、59 或 68 在总体(调整流行率比值 = 1.14,95% CI = 1.03 至 1.26;P = .011)或艾滋病毒感染者(调整流行率比值 = 1.00,95% CI = 0.83 至 1.21。P = 0.99)中均未见保护作用:这些数据提供了令人欣慰的证据,证明单剂量对南非人群中的 HPV 16 和 18 流行率有影响,与艾滋病毒感染状况无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of single-dose HPV vaccination on HPV 16 and 18 prevalence in South African adolescent girls with and without HIV.

Background: The World Health Organization has endorsed single-dose human papillomavirus (HPV) vaccination, but data on the impact on HPV prevalence in high HIV burden settings are limited.

Methods: A single-dose bivalent HPV vaccine was delivered to adolescent girls in grade 10 in a schools-based campaign in 1 district in South Africa. Impact on HPV 16 and 18 prevalence was evaluated using repeat cross-sectional surveys. A clinic-based survey in girls aged 17-18 years established HPV 16 and 18 prevalence in a prevaccine population (n = 506, including 157 living with HIV) in 2019 and was repeated in the same age group and sites in a single-dose eligible population in 2021 (n = 892, including 117 with HIV). HPV DNA was detected on self-collected vaginal swabs using the Seegene Anyplex II HPV 28. Population impact was estimated overall and by HIV status using prevalence ratios adjusted for differences in sexual behavior between surveys.

Results: Single-dose vaccination campaign coverage was 72% (4807 of 6673) of eligible girls attending high school (n = 66) in the district. HPV 16 and 18 prevalence was 35% lower in the postvaccine survey overall (adjusted prevalence ratio = 0.65, 95% confidence interval [CI] = 0.51 to 0.83; P < .001) and 37% lower in those living with HIV (adjusted prevalence ratio = 0.63, 95% CI = 0.41 to 0.95; P  = .026). No protective effect was seen for nonvaccine oncogenic HPV types 33, 35, 39, 51, 52, 56, 58, 59, or 68 overall (adjusted prevalence ratio = 1.14, 95% CI = 1.03 to 1.26; P = .011) or in those living with HIV (adjusted prevalence ratio = 1.00, 95% CI = 0.83 to 1.21. P = 0.99).

Conclusion: These data provide reassuring evidence of single-dose impact on population-level HPV 16 and 18 prevalence in a South African population, irrespective of HIV status.

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