Targeting Innate Immunity to Enhance the Efficacy of Radiation Therapy

Front Immunol. 2019 Jan 14:9:3077. doi: 10.3389/fimmu.2018.03077. eCollection 2018.

Abstract

Radiation continues to play a major role in the treatment of almost every cancer type. Traditional radiation studies focused on its ability to damage DNA, but recent evidence has demonstrated that a key mechanism driving the efficacy of radiation in vivo is the immune response triggered in irradiated tissue. Innate immune cells including macrophages, dendritic cells, and natural killer cells are key mediators of the radiation-induced immune response. They regulate the sensing of radiation-mediated damage and subsequent radiation-induced inflammation. Given the importance of innate immune cells as determinants of the post-radiation anti-tumor immune response, much research has been devoted to identify ways to both enhance the innate immune response and prevent their ability to suppress ongoing immune responses. In this review, we will discuss how the innate immune system shapes anti-tumor immunity following radiation and highlight key strategies directed at the innate immune response to enhance the efficacy of radiation.

Keywords: NK cells; dendritic cells; immunotherapy; innate and adaptive immune response; macrophages; radiation therapy.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Adaptive Immunity / drug effects*
  • Adaptive Immunity / radiation effects
  • Antineoplastic Agents, Immunological / pharmacology
  • Antineoplastic Agents, Immunological / therapeutic use*
  • Chemoradiotherapy / methods
  • Clinical Trials as Topic
  • Dendritic Cells / drug effects
  • Dendritic Cells / immunology
  • Dendritic Cells / radiation effects
  • Humans
  • Immunity, Innate / drug effects*
  • Immunity, Innate / radiation effects
  • Killer Cells, Natural / drug effects
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / radiation effects
  • Macrophages / drug effects
  • Macrophages / immunology
  • Macrophages / radiation effects
  • Molecular Targeted Therapy / methods
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • Treatment Outcome
  • Tumor Microenvironment / drug effects
  • Tumor Microenvironment / immunology
  • Tumor Microenvironment / radiation effects*

Substances

  • Antineoplastic Agents, Immunological