Tumor immune microenvironment and the current immunotherapy of cholangiocarcinoma (Review)

Int J Oncol. 2023 Dec;63(6):137. doi: 10.3892/ijo.2023.5585. Epub 2023 Oct 27.

Abstract

Cholangiocarcinoma (CCA) is a highly heterogeneous malignancy originating from the epithelial system of the bile ducts, and its incidence in recent years is steadily increasing. The immune microenvironment of CCA is characterized by diversity and complexity, with a substantial presence of cancer‑associated fibroblasts and immune cell infiltration, which plays a key role in regulating the distinctive biological behavior of cholangiocarcinoma, including tumor growth, angiogenesis, lymphangiogenesis, invasion and metastasis. Despite the notable success of immunotherapy in the treatment of solid tumors in recent years, patients with CCA have responded poorly to immune checkpoint inhibitor therapy. The interaction of tumor cells with cellular components of the immune microenvironment can regulate the activity and function of immune cells and form an immunosuppressive microenvironment, which may cause ineffective immunotherapy. Therefore, the components of the tumor immune microenvironment appear to be novel targets for immune therapies. Combination therapy focusing on immune checkpoint inhibitors is a promising and valuable first‑line or translational treatment approach for intractable biliary tract malignancies. The present review discusses the compositional characteristics and regulatory factors of the CCA immune microenvironment and the possible immune escape mechanisms. In addition, a summary of the advances in immunotherapy for CCA is also provided. It is hoped that the present review may function as a valuable reference for the development of novel immunotherapeutic strategies for CCA.

Keywords: cholangiocarcinoma; immune checkpoint inhibitor; immune microenvironment; immunotherapy.

Publication types

  • Review

MeSH terms

  • Bile Duct Neoplasms* / pathology
  • Bile Duct Neoplasms* / therapy
  • Bile Ducts, Intrahepatic / pathology
  • Cancer-Associated Fibroblasts* / pathology
  • Cholangiocarcinoma* / pathology
  • Cholangiocarcinoma* / therapy
  • Humans
  • Immunotherapy
  • Tumor Microenvironment

Grants and funding

The present study was supported by the 1.3.5 project for disciplines of excellence, West China Hospital, Sichuan University (grant no. ZYJC21046); the 1.3.5 project for disciplines of excellence-Clinical Research Incubation Project, West China Hospital, Sichuan University (grant no. 2021HXFH001); the Natural Science Foundation of Sichuan Province (grant no. 2022NSFSC0806); the National Natural Science Foundation of China for Young Scientists Fund (grant no. 82203782), Sichuan Science and Technology Program (grant nos. 2021YJ0132 and 2021YFS0100); the fellowship of China Postdoctoral Science Foundation (grant no. 2021M692277); the Sichuan University-Zigong School-local Cooperation project (grant no. 2021CDZG-23); the Science and Technology project of the Health planning committee of Sichuan (21PJ046); and the Post-Doctor Research Project, West China Hospital, Sichuan University (grant no. 2021HXBH127).