Engineering macrophages to phagocytose cancer cells by blocking the CD47/SIRPɑ axis

Cancer Med. 2019 Aug;8(9):4245-4253. doi: 10.1002/cam4.2332. Epub 2019 Jun 11.

Abstract

The use of immunotherapy has achieved great advances in the treatment of cancer. Macrophages play a pivotal role in the immune defense system, serving both as phagocytes (removal of pathogens and cancer cells) and as antigen-presenting cells (activation of T cells). However, research regarding tumor immunotherapy is mainly focused on the adaptive immune system. The usefulness of innate immune cells (eg, macrophages) in the treatment of cancer has not been extensively investigated. Recent advances in synthetic biology and the increasing understanding of the cluster of differentiation 47/signal regulatory protein alpha (CD47/SIRPɑ) axis may provide new opportunities for the clinical application of engineered macrophages. The CD47/SIRPɑ axis is a major known pathway, repressing phagocytosis and activation of macrophages. In this article, we summarize the currently available evidence regarding the CD47/SIRPɑ axis, and immunotherapies based on blockage. In addition, we propose cell therapy strategies based on macrophage engineering.

Keywords: CD47; SIRPɑ; cancer; immunotherapy; macrophages.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antigens, Differentiation / metabolism*
  • CD47 Antigen / metabolism*
  • Clinical Trials as Topic
  • Humans
  • Immunotherapy
  • Macrophages / immunology
  • Macrophages / transplantation*
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • Phagocytosis
  • Receptors, Immunologic / metabolism*
  • Signal Transduction
  • Synthetic Biology

Substances

  • Antigens, Differentiation
  • CD47 Antigen
  • CD47 protein, human
  • Receptors, Immunologic
  • SIRPA protein, human