ORIGINAL RESEARCH article
Front. Immunol.
Sec. Cancer Immunity and Immunotherapy
Volume 16 - 2025 | doi: 10.3389/fimmu.2025.1612761
This article is part of the Research TopicCancer ImmunosurveillanceView all 6 articles
Serum profiling of the antibody response to HPV in women with or without abnormal cervical cytology undergoing cervical cancer screening
Provisionally accepted- 1Department of Microbiology and Immunology, Faculty of Pharmacy, Alexandria University, Alexandria, Egypt
- 2Department of Family and Community Medicine, College of Medicine, The Pennsylvania State University, Hershey, Pennsylvania, United States
- 3Center for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, Arizona, United States
- 4Division of Population Health Sciences, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, United States
- 5Division of Health Behavior and Health Promotion, College of Public Health, The Ohio State University, Columbus, Ohio, United States
- 6Medical School, University of Michigan, Ann Arbor, Michigan, United States
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Understanding the humoral immune response to HPV is important for understanding the natural history of infection and developing biomarkers for early detection of cervical cancer. This has been technically limited by HPV type diversity and challenges of highthroughput protein expression and display. This study aimed to profile the humoral immune response to the proteomes of 12 HPV types in women with or without abnormal cervical cytology undergoing cervical cancer screening. Methods: To detect serum antibodies (Abs) against HPV, we developed custom HPV high-density diffusion-free nucleic acid programmable protein arrays (HD-NAPPA) displaying the proteomes of 2 low-risk (HPV6 and 11) and 10 highrisk (HR) HPV types (HPV16,18,31,33,35,39,45,51, 52 and 58). Arrays were probed with sera from women undergoing screening for cervical cancer, with normal (n=82) or abnormal (n=54) cervical cytology. HPV DNA testing and typing were done on cytology samples from all participants using an assay that detects 37 HPV types. Results: Abs to any HPV protein were detected in 47.6% (95% C.I.: 36.5-58.8%) and 40.7% (95% C.I.: 27.9-54.9%) of women with normal and abnormal cytology, respectively and in 44.9% (95% C.I.: 36.4-53.6%) of all women. HPV16 DNA was the most frequently detected type (36.8%, 95% C.I.: 27.4-47.4%), however, Abs against HPV16 were remarkably the least frequently detected (7.4%, 95% C.I.: 3.8-13.5%). The most frequently detected Abs were against L1, in 30.1% (95% C.I.: 22.7-38.7%) of all women (31.7% and 27.8% of women with normal and abnormal Pap, respectively). Abs against E1 and E4 were the most (in 24.3%, 95% C.I.: 17.5-32.5%) and least (13.2%, 95% C.I.: 8.2-20.4%) frequently detected E-Abs in all women, respectively. Among all subjects with antibodies to either L1 or L2, 39.0% (95% C.I.: 24.6-55.5%) of those with L1 antibodies and 51.9% (95% C.I.: 32.4-70.8%) of those with L2 antibodies were positive for the antigen from only one HPV type.Our findings shed light on the kinetics of HPV-specific humoral immunity in women with normal or abnormal cervical cytology and highlight the need for comprehensive immune profiling in different health and disease stages.
Keywords: Antibodies, HPV, cervical cancer, Cervical Intraepithelial Neoplasia, NAPPA, Protein Microarrays, Serology, early detection Abs, antibodies
Received: 16 Apr 2025; Accepted: 14 Jul 2025.
Copyright: © 2025 Ewaisha, Ruffin, Williams, Chung, Degraffinreid, Paskett, Reiter, Qiu, Brenner and Anderson. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Karen Anderson, Center for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, 85281, Arizona, United States
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