Novel Forms of Immunomodulation for Cancer Therapy

Trends Cancer. 2020 Jun;6(6):518-532. doi: 10.1016/j.trecan.2020.02.015. Epub 2020 Mar 31.

Abstract

In recent years immunotherapy has provided new hope for cancer patients. However, some patients eventually relapse. Immunological responses are thought to underlie the long-term effects of conventional or targeted therapies. Whether this influence emerges from direct effects on cancer cells through immunogenic cell death (ICD) or by modulating the immune environment requires further clarification. ICD-related molecular mechanisms are also shared by cell-intrinsic defense responses that combat foreign intrusions. Indeed, we could potentially mimic and harness these processes to improve cancer immunogenicity. In addition, the microbiome is materializing as a missing factor in the cancer-immune therapy axis. The emerging idea of manipulating the gut microbiota to improve responses to anticancer therapy is becoming increasingly popular, but further clinical authentication is needed.

Keywords: cancer immunotherapy; immunogenic cell death; microbiota, immunomodulation.

Publication types

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

MeSH terms

  • Administration, Metronomic
  • Alarmins / immunology
  • Alarmins / metabolism
  • Animals
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage*
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Bacterial Translocation / drug effects
  • Bacterial Translocation / immunology
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Dose-Response Relationship, Immunologic
  • Dysbiosis / chemically induced
  • Dysbiosis / immunology
  • Dysbiosis / microbiology
  • Dysbiosis / prevention & control*
  • Gastrointestinal Microbiome / drug effects*
  • Gastrointestinal Microbiome / immunology
  • Humans
  • Immunogenic Cell Death / drug effects
  • Immunogenic Cell Death / immunology
  • Immunotherapy / adverse effects
  • Immunotherapy / methods*
  • Immunotherapy / trends
  • Killer Cells, Natural / drug effects
  • Killer Cells, Natural / immunology
  • Lymphocyte Depletion / methods
  • Maximum Tolerated Dose
  • Mice
  • Myeloid-Derived Suppressor Cells / drug effects
  • Myeloid-Derived Suppressor Cells / immunology
  • Neoplasms / immunology
  • Neoplasms / microbiology
  • Neoplasms / therapy*
  • Pathogen-Associated Molecular Pattern Molecules / immunology
  • Pathogen-Associated Molecular Pattern Molecules / metabolism
  • Signal Transduction / drug effects
  • Signal Transduction / immunology
  • T-Lymphocytes, Regulatory / drug effects
  • T-Lymphocytes, Regulatory / immunology

Substances

  • Alarmins
  • Pathogen-Associated Molecular Pattern Molecules