Immune Microenvironment and Immunotherapeutic Management in Virus-Associated Digestive System Tumors

Int J Mol Sci. 2022 Nov 6;23(21):13612. doi: 10.3390/ijms232113612.

Abstract

The development of cancer is a multifactorial phenomenon, while it constitutes a major global health problem. Viruses are an important factor that is involved in tumorigenesis and is associated with 12.1% of all cancer cases. Major examples of oncogenic viruses which are closely associated with the digestive system are HBV, HCV, EBV, HPV, JCV, and CMV. EBV, HPV, JCV, and CMV directly cause oncogenesis by expressing oncogenic proteins that are encoded in their genome. In contrast, HBV and HCV are correlated indirectly with carcinogenesis by causing chronic inflammation in the infected organs. In addition, the tumor microenvironment contains various immune cells, endothelial cells, and fibroblasts, as well as several growth factors, cytokines, and other tumor-secreted molecules that play a key role in tumor growth, progression, and migration, while they are closely interrelated with the virus. The presence of T-regulatory and B-regulatory cells in the tumor microenvironment plays an important role in the anti-tumor immune reaction. The tumor immune microenvironments differ in each type of cancer and depend on viral infection. The alterations in the immune microenvironment caused by viruses are also reflected in the effectiveness of immunotherapy. The present review aims at shedding light on the association between viruses and digestive system malignancies, the characteristics of the tumor immune microenvironment that develop, and the possible treatments that can be administered.

Keywords: CMV; EBV; HBV; HCV; HPV; JCV; digestive system; immunotherapy; tumor immune microenvironment.

Publication types

  • Review

MeSH terms

  • Carcinogenesis
  • Cell Transformation, Neoplastic
  • Cytomegalovirus Infections*
  • Endothelial Cells
  • Gastrointestinal Neoplasms*
  • Hepatitis C*
  • Humans
  • Immunotherapy
  • Papillomavirus Infections*
  • Tumor Microenvironment

Grants and funding

This work received no external funding.