MHC Class I Deficiency in Solid Tumors and Therapeutic Strategies to Overcome It

Int J Mol Sci. 2021 Jun 23;22(13):6741. doi: 10.3390/ijms22136741.

Abstract

It is now well accepted that the immune system can control cancer growth. However, tumors escape immune-mediated control through multiple mechanisms and the downregulation or loss of major histocompatibility class (MHC)-I molecules is a common immune escape mechanism in many cancers. MHC-I molecules present antigenic peptides to cytotoxic T cells, and MHC-I loss can render tumor cells invisible to the immune system. In this review, we examine the dysregulation of MHC-I expression in cancer, explore the nature of MHC-I-bound antigenic peptides recognized by immune cells, and discuss therapeutic strategies that can be used to overcome MHC-I deficiency in solid tumors, with a focus on the role of natural killer (NK) cells and CD4 T cells.

Keywords: MHC-I; NK cells; T-cell subsets; immune checkpoint blockade; immunotherapy; major histocompatibility complex (MHC); tumor antigen presentation; tumor antigens.

Publication types

  • Review

MeSH terms

  • Animals
  • Antigens, Neoplasm / immunology*
  • CD4-Positive T-Lymphocytes / immunology
  • Down-Regulation
  • Histocompatibility Antigens Class I / genetics*
  • Histocompatibility Antigens Class I / immunology
  • Histocompatibility Antigens Class I / metabolism*
  • Humans
  • Immunotherapy / methods
  • Killer Cells, Natural / immunology
  • Mutation
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • Tumor Escape / physiology*

Substances

  • Antigens, Neoplasm
  • Histocompatibility Antigens Class I