Minimally invasive diagnosis of precancerous cervical lesions using single-cell peripheral immune atlas.
cross_sectional · Level IV
Where this comes from
- Record sourced from PubMed, PMID 40412381.
- Also identified by DOI 10.1016/j.xcrm.2025.102149 and PMC identifier 12208321.
- Licence recorded as CC BY-NC-ND.
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Abstract
Cervical cancer remains a major global health concern for women. Current screening methods are either invasive or lead to low participation and over-referral for colposcopy, particularly among high-risk human papillomavirus (HPV)-positive women. This study analyzes 613 participants with varying cervical lesions using mass cytometry by time-of-flight (CyTOF) to identify disease-specific peripheral immune signatures. A diagnostic model based on 23 immune features achieves ∼91% sensitivity and specificity for detecting precancerous and cancerous lesions. A separate model for HPV-positive women shows even higher accuracy (∼93% sensitivity, ∼95% specificity), especially in HPV16/18-positive cases (99% sensitivity, 100% specificity). In an independent validation cohort (n = 105), the model distinguishes cervical intraepithelial neoplasia (CIN) 2+ from ≤CIN1 with 86.5% sensitivity and 85.3% specificity (area under the curve [AUC] = 0.89). These findings support peripheral immune profiling as a minimally invasive and accurate biomarker strategy for early cervical cancer screening, particularly in HPV16/18-positive women.
Medical subject headings
- Uterine Cervical Neoplasms
- Uterine Cervical Dysplasia
- Precancerous Conditions
- Single-Cell Analysis