Effectiveness and immune responses of focused ultrasound ablation for cervical intraepithelial neoplasia

Int J Hyperthermia. 2022;39(1):539-546. doi: 10.1080/02656736.2022.2052365.

Abstract

Purpose: To investigate the safety, efficacy, and the immune responses of focused ultrasound in cervical intraepithelial neoplasia (CIN).

Methods: Patients with biopsy-confirmed CIN were recruited for focused ultrasound treatment and asked to return during 3-6 and 6-12 months post-treatment to receive cervical cytology, high-risk human papilloma virus (HPV) detection, and colposcopy. The effective rate was evaluated within 3-6 months, whereas the recurrence rate was evaluated within 6-12 months. Cervicovaginal lavage and cervical tissue were sampled before and 3-6 months after treatment. The expression of interferon gamma (IFN-γ), endoplasmic reticulum aminopeptidase 1 (ERAP1), human leucocyte antigen I (HLA-I), cluster of differentiation 4 (CD4), and cluster of differentiation 8 (CD8) in the cervical tissue were observed by immunohistochemistry. Immunoglobulin A (IgA) and interleukin 10 (IL-10) levels in the cervicovaginal lavage were detected by enzyme-linked immunosorbent assay. Comparisons were made in immune analyte levels before and after treatment.

Results: We analyzed the results of 154 patients. The effective rate at 3-6 months was 96.8%. The recurrence rate at 6-12 months was 2.0%. The eradication rate of HPV was 72.4% at 3-6 months and 81.0% at 6-12 months. No serious adverse reactions and complications were observed. After treatment, a higher expression of ERAP1 was observed (p < 0.05). Significant down-regulation of IgA and IL-10 were detected (each p < 0.05). However, the expression of CD4, CD8, HLA-I, as well as the release of IFN-γ, did not reach statistical significance (each p > 0.05).

Conclusions: Focused ultrasound is an effective and safe therapy for treating CIN, which could improve the local immune milieu of the cervix to some extent.

Keywords: FUS; HPV; cervical intraepithelial neoplasia; effectiveness; immune.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminopeptidases
  • Female
  • High-Intensity Focused Ultrasound Ablation*
  • Humans
  • Immunity
  • Interferon-gamma
  • Minor Histocompatibility Antigens
  • Uterine Cervical Dysplasia* / immunology
  • Uterine Cervical Dysplasia* / surgery
  • Uterine Cervical Neoplasms* / immunology
  • Uterine Cervical Neoplasms* / surgery

Substances

  • Minor Histocompatibility Antigens
  • Interferon-gamma
  • Aminopeptidases
  • ERAP1 protein, human