坦桑尼亚姆万扎孕妇中人类乳头瘤病毒 6、11、16 和 18 的血清阳性反应率。

IF 3.1 2区 医学 Q3 IMMUNOLOGY
Fridolin Mujuni, Betrand Msemwa, Vicent E Fukuru, Vitus Silago, Mariam M Mirambo, Stephen E Mshana, Balthazar Gumodoka
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引用次数: 0

摘要

导言:众所周知,高危人类乳头瘤病毒 16 和 18(HR-HPV 16 和 HR-HPV-18)与宫颈癌、头颈癌、阴茎癌和肛门癌有关。低危型人乳头瘤病毒 6 和 11(LR-HPV 6 和 LR 11)感染与儿童肛门疣、口腔乳头状瘤和喉乳头状瘤病有关。孕期感染 HPV(HR-HPV 和 LR-HPV)会增加受感染孕妇向胎儿垂直传播的风险。在产前检查诊所(ANC)就诊的孕妇中,HR-HPV 16 型和 18 型以及 LR-HPV 6 型和 11 型的感染情况尚无详细记录。本研究确定了在坦桑尼亚姆万扎布甘多医疗中心(BMC)接受产前检查的孕妇中 HR-HPV 16、18 型和 LR-HPV 6、11 型抗体的血清流行率和分布情况:2020年11月至2021年3月期间,在姆万扎布甘多医疗中心(BMC)开展了一项横断面研究,共有255名孕妇在妇产科门诊就诊。调查使用了一份预先测试过的结构化问卷来获取患者信息。采用三明治酶联免疫吸附试验(ELISA)检测血清中的HPV 6、11、16和18特异性免疫球蛋白G(IgG)。使用Stata 15v1版本进行描述性数据分析:中位年龄为 27(IQR:22-31)岁。HPV6、11、16和18型阳性者分别占37.6%(97/255)、32.2%(83/255)、15.5%(40/255)和27.1%(70)。有 8 名参与者(3.1%)对所有 4 种基因型均呈阳性:结论:约三分之二的孕妇体内有针对 HPV 6、11、16 和 18 的抗体,这表明她们曾接触过 HPV。应重视疫苗接种计划,以减少该人群中与人乳头瘤病毒相关的表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Seroprevalence of human papilloma virus 6, 11, 16 and 18 among pregnant women in Mwanza-Tanzania.

Introduction: High-risk human-papilloma viruses 16 and 18 (HR-HPV 16 and HR-HPV-18) are well known to be associated with carcinoma of the cervix, head and neck, penis, and anus. Low-risk human papillomaviruses 6 and 11 (LR-HPV 6 and LR 11) infection has been associated with anogenital warts, oral papilloma, and laryngeal papillomatosis in children. HPV infection during pregnancy (HR-HPV and LR-HPV) increases the risk of vertical transmission from infected pregnant women to unborn children. The burden of HR-HPV type 16 and 18 and LR-HPV 6 and 11 is not well documented among pregnant women attending antenatal clinics (ANC). This study determined the seroprevalence and distributions of HR-HPV 16, 18, and LR -HPV 6, 11 antibodies among pregnant women attending ANC at Bugando Medical Centre (BMC) in Mwanza, Tanzania.

Methodology: A cross-sectional study involving 255 pregnant women enrolled in obstetrics and gynecology outpatient clinics was conducted between November 2020 and March 2021 at Bugando Medical Centre (BMC) in Mwanza. A structured pre-tested questionnaire was used to obtain patients' information. Sandwich Enzyme-Linked Immunosorbent Assay (ELISA) was used to detect HPV 6, 11, 16 and 18 specific immunoglobulin G (IgG) from sera. Stata version 15v1 was used for the descriptive data analysis.

Results: The median age was 27(IQR: 22-31) years. The overall HPV seropositivity for any of the four serotypes was 63.9% (165/255), 95% CI: 58.0-69.7, whereby 37.6%(97/255), 32.2%( 83/255), 15.5% (40/255) and 27.1% (70) were positive for HPV 6, 11, 16 and 18 respectively. Eight participants (3.1%) were positive for all 4 genotypes.

Conclusion: About two-thirds of pregnant women had antibodies against HPV 6, 11 16, and 18 indicating previous HPV exposure. Vaccination programs should be emphasized to reduce the HPV-related manifestations in this population.

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来源期刊
Infectious Agents and Cancer
Infectious Agents and Cancer ONCOLOGY-IMMUNOLOGY
CiteScore
5.80
自引率
2.70%
发文量
54
期刊介绍: Infectious Agents and Cancer is an open access, peer-reviewed online journal that encompasses all aspects of basic, clinical, epidemiological and translational research providing an insight into the association between chronic infections and cancer. The journal welcomes submissions in the pathogen-related cancer areas and other related topics, in particular: • HPV and anogenital cancers, as well as head and neck cancers; • EBV and Burkitt lymphoma; • HCV/HBV and hepatocellular carcinoma as well as lymphoproliferative diseases; • HHV8 and Kaposi sarcoma; • HTLV and leukemia; • Cancers in Low- and Middle-income countries. The link between infection and cancer has become well established over the past 50 years, and infection-associated cancer contribute up to 16% of cancers in developed countries and 33% in less developed countries. Preventive vaccines have been developed for only two cancer-causing viruses, highlighting both the opportunity to prevent infection-associated cancers by vaccination and the gaps that remain before vaccines can be developed for other cancer-causing agents. These gaps are due to incomplete understanding of the basic biology, natural history, epidemiology of many of the pathogens that cause cancer, the mechanisms they exploit to cause cancer, and how to interrupt progression to cancer in human populations. Early diagnosis or identification of lesions at high risk of progression represent the current most critical research area of the field supported by recent advances in genomics and proteomics technologies.
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