Evidence map›Paper›PMID 40821832›Full record

ArticleFrontiers in immunology2025

Serum profiling of the antibody response to HPV in women with or without abnormal cervical cytology undergoing cervical cancer screening.

Radwa Ewaisha, Mack T Ruffin, Stacy Williams, Yunro Chung, Cecilia R DeGraffinreid, Electra D Paskett, Paul L Reiter, Ji Qiu, Dean E Brenner, Karen S Anderson

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Radwa EwaishaDepartment of Microbiology and Immunology, Faculty of Pharmacy, Alexandria University, Alexandria, Egypt.
Mack T RuffinDepartment of Family and Community Medicine, Penn State College of Medicine, Hershey, PA, United States.
Stacy WilliamsCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ, United States.
Yunro ChungCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ, United States.
Cecilia R DeGraffinreidDivision of Population Health Sciences, Ohio State University Comprehensive Cancer Center, Columbus, OH, United States.
Electra D PaskettDivision of Population Health Sciences, Ohio State University Comprehensive Cancer Center, Columbus, OH, United States.
Paul L ReiterDivision of Health Behavior and Health Promotion, College of Public Health, The Ohio State University, Columbus, OH, United States.
Ji QiuCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ, United States.
Dean E BrennerDepartment of Pharmacology, University of Michigan Medical School, Ann Arbor, MI, United States.
Karen S AndersonCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: 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 high-throughput 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 high-risk (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. Conclusion: 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.

Indexed as

Antibodies, ViralPapillomaviridaePapillomavirus InfectionsUterine Cervical NeoplasmsAdultAgedEarly Detection of CancerFemaleHumansMiddle AgedAntibodies, Viralantibodiescervical cancercervical intraepithelial neoplasiaearly detection antibodiesHPVNAPPAprotein microarraysserology

Identifiers

PMID40821832
PMCPMC12350350

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.