[Evaluation of the 10-year protective effect and immunogenicity of quadrivalent HPV vaccination].

C H Pan, X Q Xu, T M Wen, M Y Wang, J F Ma, J X Han, S H Li, S Y Hu, Y L Qiao, F H Zhao
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Abstract

Objective: To evaluate the 10-year protective effect and immunogenicity of quadrivalent human papillomavirus (HPV) vaccine in Chinese women aged 20 to 45 years. Methods: From October 2019 to April 2020, a long-term follow-up study was conducted on the subjects of the Phase III clinical trial of the quadrivalent HPV vaccine (NCT00834106). Participants underwent a questionnaire survey, venous blood sampling, gynecological examination, cervical exfoliated cell pathology examination, and serum neutralizing antibody titers for HPV-6, 11, 16, and 18 were measured using a pseudovirus neutralization assay. The results of the cytological examination and the positive rate and titers of serum antibodies of different cervical exfoliated cells were compared. Results: A total of 889 subjects were followed up, including 240 in the control group, 453 in the vaccination group and 196 in the post-trial vaccination group. The age of the control group was (40±7) years old, which was higher than that of the supplementary vaccination group and the vaccination group [(38±4) and (38±6) years old, respectively] (P<0.05). There were no statistically significant differences in condom use and sexual frequency among all groups (all P values>0.05). The abnormal proportion of cervical exfoliation cytopathology in the vaccination group was 3.7% (17/453), which was significantly lower than that in the control group [9.6% (23/240)] and post-trial vaccination group [5.6% (11/196)] (P<0.05). There were two cases of cervical intraepithelial neoplasia (CIN) grade 1 in the vaccination group, two cases of CIN grade 1 and three cases of CIN grade 2 and above in the control group, and no CIN grade 1 and above cases in the post-trial vaccination group. The positive rate of HPV-18 antibody was 35.5% (161/453) in the vaccination group and 76.0% (149/196) in the post-trial vaccination group, which was significantly lower than that of other types (P<0.05). The neutralizing antibody GMT ratio between the vaccination group and the control group ranged from 2.62 to 25.33 (9.05 to 83.08). Conclusion: Protective neutralizing antibodies are sustained in Chinese women aged 20 to 45 years after ten years of vaccination with quadrivalent HPV vaccine.

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[评估四价人乳头瘤病毒疫苗的 10 年保护效果和免疫原性]。
目的评估四价人乳头瘤病毒 (HPV) 疫苗对 20 至 45 岁中国女性的 10 年保护效果和免疫原性。方法2019年10月至2020年4月,对四价HPV疫苗III期临床试验(NCT00834106)的受试者进行了长期随访研究。受试者接受了问卷调查、静脉采血、妇科检查、宫颈脱落细胞病理学检查,并使用假病毒中和检测法测定了血清中的 HPV-6、11、16 和 18 中和抗体滴度。比较了细胞学检查结果和不同宫颈脱落细胞的阳性率及血清抗体滴度。研究结果共对 889 名受试者进行了随访,其中对照组 240 人,接种组 453 人,试验后接种组 196 人。对照组的年龄为(40±7)岁,高于补充接种组和接种组[分别为(38±4)岁和(38±6)岁](PP 值>0.05)。疫苗接种组宫颈脱落细胞病理学异常比例为 3.7%(17/453),显著低于对照组[9.6%(23/240)]和试验后疫苗接种组[5.6%(11/196)](PPC结论:保护性中和抗体可持续存在于疫苗接种组和试验后疫苗接种组中:接种四价人乳头瘤病毒疫苗十年后,20 至 45 岁中国女性体内的保护性中和抗体可持续存在。
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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来源期刊
中华预防医学杂志
中华预防医学杂志 Medicine-Medicine (all)
CiteScore
1.20
自引率
0.00%
发文量
12678
期刊介绍: Chinese Journal of Preventive Medicine (CJPM), the successor to Chinese Health Journal , was initiated on October 1, 1953. In 1960, it was amalgamated with the Chinese Medical Journal and the Journal of Medical History and Health Care , and thereafter, was renamed as People’s Care . On November 25, 1978, the publication was denominated as Chinese Journal of Preventive Medicine . The contents of CJPM deal with a wide range of disciplines and technologies including epidemiology, environmental health, nutrition and food hygiene, occupational health, hygiene for children and adolescents, radiological health, toxicology, biostatistics, social medicine, pathogenic and epidemiological research in malignant tumor, surveillance and immunization.
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