Clinical significance of immune checkpoint proteins in HPV-infected cervical cancer

J Infect Public Health. 2023 Apr;16(4):542-550. doi: 10.1016/j.jiph.2023.01.019. Epub 2023 Jan 31.

Abstract

Objective: To investigate T cell immunoreceptor with Ig and ITIM domain (TIGIT), V-domain Ig suppressor of T cell activation (VISTA), and lymphocyte-activation gene-3 (LAG-3) expression in pathological tissue of human papillomavirus (HPV)-infected cervical cancer (CC) patients and their relationship with patient prognosis.

Methods: Clinical data of 175 patients with HPV-infected CC were collected retrospectively. Tumor tissue sections were stained immunohistochemically for TIGIT, VISTA, and LAG-3. The Kaplan-Meier method calculated patient survival. Univariate and multivariate Cox proportional hazards models analyzed all potential risk factors for survival.

Results: When combined positive score (CPS)= 1 was used as the cut-off value, the Kaplan-Meier survival curve showed that the progression-free survival (PFS) and overall survival (OS) of patients with positive expression of TIGIT and VISTA are shorter (both p < 0.05). Univariate COX regression analysis showed that the positive expression of TIGIT and VISTA are related to patient PFS and OS (both HR>1.0 and p < 0.05). Multivariate COX regression analysis showed that TIGIT-positive patients had shorter OS and VISTA-positive patients had shorter PFS (both HR>1.0 and p < 0.05). There is no significant correlation between LAG-3 expression and PFS or OS. When CPS= 10 was used as the cut-off value, Kaplan-Meier survival curve showed that TIGIT-positive patients had shorter OS (p = 0.019). Univariate COX regression analysis showed that TIGIT-positive expression was associated with the OS of patients (HR=2.209, CI: 1.118-4.365, p = 0.023). However, multivariate COX regression analysis showed that TIGIT expression was not associated significantly with OS. There was no significant correlation between VISTA and LAG-3 expression and PFS or OS.

Conclusion: TIGIT and VISTA are associated closely with HPV-infected CC prognosis and are effective biomarkers.

Keywords: Cervical cancer; HPV; Immune checkpoints; LAG-3; TIGIT; VISTA.

MeSH terms

  • Clinical Relevance
  • Female
  • Human Papillomavirus Viruses
  • Humans
  • Immune Checkpoint Proteins
  • Papillomavirus Infections* / complications
  • Prognosis
  • Receptors, Immunologic
  • Retrospective Studies
  • Uterine Cervical Neoplasms*

Substances

  • Immune Checkpoint Proteins
  • Receptors, Immunologic