Prognostic impact of CD8+ T cell distribution and its association with the HLA class I expression in intrahepatic cholangiocarcinoma

Surg Today. 2020 Aug;50(8):931-940. doi: 10.1007/s00595-020-01967-y. Epub 2020 Feb 10.

Abstract

Purpose: A lack of effective systemic therapy is one reason for the poor prognosis of intrahepatic cholangiocarcinoma. Newly developed immune checkpoint inhibitors function by minimizing CD8+ T cell suppression to improve tumor-specific responses. This study aimed to examine the characteristics of CD8+ T cells in intrahepatic cholangiocarcinoma.

Methods: Clinicopathological data, including the overall survival, of 69 cases of postoperative intrahepatic cholangiocarcinoma were prospectively investigated. We then immunohistochemically stained for CD8, Foxp3, CD163, PD-L1, and human leukocyte antigen (HLA) class I and counted the number of CD8+ T cells, Foxp3+ T cells, and CD163+ macrophages in different areas (outer border, interborder, and intratumor).

Results: A significant difference was found in the 5-year overall survival between the CD8+ T cell high group (45.5%) and low group (24.7%) in the outer border area (p = 0.0103). Furthermore, the number of CD8+ T cells and the high expression of HLA class I were positively correlated (p = 0.0341).

Conclusion: The number of CD8+ T cells in the outer border area of the tumor correlated with the HLA class I expression of intrahepatic cholangiocarcinoma and may therefore be a prognostic factor for patients with postoperative intrahepatic cholangiocarcinoma.

Keywords: CD8+ T cell; Cholangiocarcinoma; HLA class I; Intrahepatic cholangiocarcinoma; PD-L1.

MeSH terms

  • Bile Duct Neoplasms / genetics*
  • Bile Duct Neoplasms / immunology*
  • Bile Duct Neoplasms / mortality
  • Bile Duct Neoplasms / surgery
  • Biliary Tract Surgical Procedures
  • CD8-Positive T-Lymphocytes / immunology*
  • Cholangiocarcinoma / genetics*
  • Cholangiocarcinoma / immunology*
  • Cholangiocarcinoma / mortality
  • Cholangiocarcinoma / surgery
  • Female
  • Gene Expression*
  • Histocompatibility Antigens Class I / genetics*
  • Histocompatibility Antigens Class I / metabolism*
  • Humans
  • Male
  • Middle Aged
  • Prognosis
  • Survival Rate

Substances

  • Histocompatibility Antigens Class I