The role of vaginal biofilms in endocervical neoplasia development: A literature review
DOI:
https://doi.org/10.37800/RM.2.2026.700Keywords:
bacterial vaginosis, biofilm, cervicovaginal microbiome, cervicovaginal mucus, human papillomavirus , cervical neoplasiaAbstract
Relevance: The persistence of infection with high-risk human papillomavirus (HPV) types is a necessary condition for the development of most precancerous lesions and cervical cancer. However, the outcome of infection is largely determined by the cervicovaginal tract microenvironment. The biofilm phenotype of bacterial vaginosis and related dysbiosis conditions are potentially modifiable cofactors for HPV persistence and neoplasia progression, including cervical canal lesions.
The study aimed to systematize current concepts regarding the roles of vaginal biofilms and the cervicovaginal barrier in the persistence of human papillomavirus and the development of cervical neoplasia.
Materials and Methods: A review of publications in PubMed/Medline and current clinical guidelines was conducted. Priority was given to systematic reviews, meta-analyses, longitudinal observational studies, and experiments describing biofilm organization, enzymatic phenotypes, properties of the mucosal barrier, and local immune signals.
Results: Dysbiosis characterized by a decrease in Lactobacillus-dominated states and an increase in anaerobic taxa is associated with impaired cervicovaginal mucus properties, altered epithelial barrier function, and enhanced local inflammation. These changes may potentially contribute to prolonged HPV persistence, delayed clearance, and maintenance of precancerous lesions. Data specifically related to cervical canal neoplasia remain limited and require further studies that account for the spatial organization of biofilms and functional barrier markers.
Conclusion: Biofilm-associated dysbiosis represents a promising approach for clarifying individual risk in women with a positive HPV test and for developing adjuvant strategies to restore a protective Lactobacillus-dominated microenvironment and the barrier function of cervicovaginal mucus.
References
1. World Health Organization. Global strategy to accelerate the elimination of cervical cancer as a public health problem [Internet]. www.who.int. 2020. Available from:
https://www.who.int/publications/i/item/9789240014107
2. Perkins RB, Guido RS, Castle PE, Chelmow D, Einstein MH, Garcia F, Huh WK, Kim JJ, Moscicki AB, Nayar R, Saraiya M, Sawaya GF, Wentzensen N, Schiffman M; 2019 ASCCP Risk-Based Management Consensus Guidelines Committee. 2019 ASCCP Risk-Based Management Consensus Guidelines for Abnormal Cervical Cancer Screening Tests and Cancer Precursors. J Low Genit Tract Dis. 2020;24(2):102-131.
https://doi.org/10.1097/LGT.0000000000000525
3. Centers for Disease Control and Prevention. Bacterial vaginosis – STI Treatment Guidelines 2021 [Internet]. www.cdc.gov. 2021. Available from:
https://www.cdc.gov/std/treatment-guidelines/bv.htm
4. Muzny CA, Balkus JE, Mitchell C, Sobel JD, Workowski KA, Marrazzo JM, Schwebke JR. Diagnosis and Management of Bacterial Vaginosis: Summary of Evidence Reviewed for the 2021 Centers for Disease Control and Prevention Sexually Transmitted Infections Treatment Guidelines. Clin Infect Dis. 2022;74(Suppl_2):S144-S151.
https://doi.org/10.1093/cid/ciac021
5. Huang R, Liu Z, Sun T, Zhu L. Cervicovaginal microbiome, high-risk HPV infection and cervical cancer: mechanisms and therapeutic potential. Microbiol Res. 2024;287:127857.
https://doi.org/10.1016/j.micres.2024.127857
6. Bautista J, Altamirano-Colina A, López-Cortés A. The vaginal microbiome in HPV persistence and cervical cancer progression. Front Cell Infect Microbiol. 2025;15:1634251.
https://doi.org/10.3389/fcimb.2025.1634251
7. Molina MA. From dysbiosis to mechanisms: Why cervicovaginal microbiome-HPV studies must catch up with biology. PLoS Pathog. 2025;21(12):e1013830.
https://doi.org/10.1371/journal.ppat.1013830
8. Li Z, Wang C, Zhang L, Wei L. The co-regulation of HPV infection by vaginal microbiota and the immune system. Virol J. 2025;22(1):334.
https://doi.org/10.1186/s12985-025-02913-5
9. Lacroix G, Gouyer V, Gottrand F, Desseyn JL. The Cervical Mucus Barrier. Int J Mol Sci. 2020;21(21):8266.
https://doi.org/10.3390/ijms21218266
10. Gutzeit O, Gulati A, Izadifar Z, Stejskalova A, Rhbiny H, Cotton J, Budnik B, Shahriar S, Goyal G, Junaid A, Ingber DE. Cervical mucus in linked human Cervix and Vagina Chips modulates vaginal dysbiosis. NPJ Womens Health. 2025;3(1):5.
https://doi.org/10.1038/s44294-025-00054-2
11. Shvartsman E, Hill JE, Sandstrom P, MacDonald KS. Gardnerella revisited: diversity, interactions, and role in bacterial vaginosis and reproductive health. Infect Immun. 2023;91(5):e00390-22.
https://doi.org/10.1128/iai.00390-22
12. Chen L, Li J, Xiao B. The role of sialidases in the pathogenesis of bacterial vaginosis. Front Cell Infect Microbiol. 2024;14:1472641.
https://doi.org/10.3389/fcimb.2024.1472641
13. Anton L, Ferguson B, Friedman ES, Gerson KD, Brown AG, Elovitz MA. Gardnerella vaginalis alters cervicovaginal epithelial cell function through microbe-specific immune responses. Microbiome. 2022;10(1):119.
https://doi.org/10.1186/s40168-022-01317-9
14. Schellekens HCJ, Schmidt LMS, Morré SA, van Esch EMG, de Vos van Steenwijk PJ. Vaginal Microbiota and Local Immunity in HPV-Induced Cervical Intraepithelial Neoplasia and Cervical Cancer. Int J Mol Sci. 2025;26(23):7254.
https://doi.org/10.3390/ijms26237254
15. Mitra A, MacIntyre DA, Lee YS, Smith A, Marchesi JR, Lehne B, Bhatia R, Lyons D, Kyrgiou M. The vaginal microbiota associates with the regression of untreated cervical intraepithelial neoplasia 2 lesions. Nat Commun. 2020;11(1):1999.
https://doi.org/10.1038/s41467-020-15856-y
16. Hodgson A, Olkhov-Mitsel E, Howitt BE, Nucci MR, Parra-Herran C. International Endocervical Adenocarcinoma Criteria and Classification (IECC): correlation with adverse clinicopathological features and patient outcome. J Clin Pathol. 2019;72(5):347-353.
https://doi.org/10.1136/jclinpath-2018-205632
17. Steinman D, Petersen AP, Chibber Y, Crawford C, Tyagi P, Zierden HC. Vaginal bacteria-derived extracellular vesicles diffuse through human cervicovaginal mucus to enable microbe-host signaling. NPJ Biofilms Microbiomes. 2026;12(1):10.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2026 Э.А. Кыдырбаева, Е.М. Изтлеуов , Г.М. Изтлеуова

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
The articles published in this Journal are licensed under the CC BY-NC-ND 4.0 (Creative Commons Attribution – Non-Commercial – No Derivatives 4.0 International) license, which provides for their non-commercial use only. Under this license, users have the right to copy and distribute the material in copyright but are not permitted to modify or use it for commercial purposes. Full details on the licensing are available at https://creativecommons.org/licenses/by-nc-nd/4.0/.
