Viral and immune dynamics of genital human papillomavirus infections in young women with high temporal resolution.

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences PLoS Biology Pub Date : 2025-01-21 eCollection Date: 2025-01-01 DOI:10.1371/journal.pbio.3002949
Nicolas Tessandier, Baptiste Elie, Vanina Boué, Christian Selinger, Massilva Rahmoun, Claire Bernat, Sophie Grasset, Soraya Groc, Anne-Sophie Bedin, Thomas Beneteau, Marine Bonneau, Christelle Graf, Nathalie Jacobs, Tsukushi Kamiya, Marion Kerioui, Julie Lajoie, Imène Melki, Jean-Luc Prétet, Bastien Reyné, Géraldine Schlecht-Louf, Mircea T Sofonea, Olivier Supplisson, Chris Wymant, Vincent Foulongne, Jérémie Guedj, Christophe Hirtz, Marie-Christine Picot, Jacques Reynes, Vincent Tribout, Édouard Tuaillon, Tim Waterboer, Michel Segondy, Ignacio G Bravo, Nathalie Boulle, Carmen Lía Murall, Samuel Alizon
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Abstract

Human papillomavirus (HPV) infections drive one in 20 new cancer cases, exerting a particularly high burden on women. Most anogenital HPV infections are cleared in less than two years, but the underlying mechanisms that favour persistence in around 10% of women remain largely unknown. Notwithstanding, it is precisely this information that is crucial for improving treatment, screening, and vaccination strategies. To understand viral and immune dynamics in non-persisting HPV infections, we set up an observational longitudinal cohort study with frequent on-site visits for biological sample collection. We enrolled 189 women aged from 18 to 25 and living in the area of Montpellier (France) between 2016 and 2020. We performed 974 on-site visits for a total of 1,619 months of follow-up. We collected data on virus load, local immune cell populations, local concentrations of cytokines, and circulating antibody titres. Using hierarchical Bayesian statistical modelling to simultaneously analyse the data from 164 HPV infections from 76 participants, we show that in two months after infection, HPV viral load in non-persisting infections reaches a plateau that lasts on average for 13 to 20 months (95% credibility interval) and is then followed by a rapid clearance phase. This first description of the dynamics of HPV infections comes with the identification of immune correlates associated with infection clearance, especially gamma-delta T cells and CXCL10 concentration. A limitation of this study on HPV kinetics is that many infection follow-ups are censored. Furthermore, some immune cell populations are difficult to label because cervical immunity is less well characterised than systemic immunity. These results open new perspectives for understanding the frontier between acute and chronic infections, and for controlling HPV-associated diseases, as well as for research on human cancers of infectious origin. Trial Registration: This trial was registered is registered at ClinicalTrials.gov under the ID NCT02946346. This study has been approved by the Comité de Protection des Personnes (CPP) Sud Méditerranée I (reference number 2016-A00712-49); by the Comité Consultatif sur le Traitement de l'Information en matière de Recherche dans le domaine de la Santé (reference number 16.504); by the Commission Nationale Informatique et Libertés (reference number MMS/ABD/ AR1612278, decision number DR-2016-488), by the Agence Nationale de Sécurité du Médicament et des Produits de Santé (reference 20160072000007).

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年轻女性生殖器人乳头瘤病毒感染的病毒和免疫动力学具有高时间分辨率。
每20个新发癌症病例中就有1人感染人类乳头瘤病毒(HPV),这对妇女造成了特别沉重的负担。大多数肛门生殖器HPV感染在不到两年的时间内就会被清除,但大约10%的女性持续感染的潜在机制在很大程度上仍然未知。然而,正是这些信息对改善治疗、筛查和疫苗接种策略至关重要。为了了解非持续性HPV感染的病毒和免疫动力学,我们建立了一项观察性纵向队列研究,经常到现场采集生物样本。我们招募了189名年龄在18至25岁之间的女性,她们在2016年至2020年期间居住在法国蒙彼利埃地区。在1,619个月的随访中,我们进行了974次现场访问。我们收集了病毒载量、局部免疫细胞群、局部细胞因子浓度和循环抗体滴度的数据。使用分层贝叶斯统计模型同时分析来自76名参与者的164例HPV感染的数据,我们表明,在感染后的两个月内,非持续性感染中的HPV病毒载量达到平均持续13至20个月的平台期(95%可信区间),然后是快速清除阶段。这是HPV感染动力学的第一次描述,伴随着与感染清除相关的免疫相关物的鉴定,特别是γ - δ T细胞和CXCL10浓度。本研究对HPV动力学的限制是,许多感染随访审查。此外,一些免疫细胞群难以标记,因为宫颈免疫不如全身免疫有很好的特征。这些结果为了解急性和慢性感染之间的前沿、控制hpv相关疾病以及研究传染性来源的人类癌症开辟了新的视角。试验注册:该试验已在ClinicalTrials.gov注册,ID为NCT02946346。本研究已获得法国人力资源保护委员会(CPP)第1届人力资源保护委员会(CPP)批准(参考编号2016-A00712-49);由圣圣领域研究和信息交换问题协商委员会(参考资料编号16.504);由国家信息和自由委员会(参考编号MMS/ABD/ AR1612278,决定编号DR-2016-488),由国家 - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -批准(参考编号20160072000007)。
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
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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