Immunotherapies inducing immunogenic cell death in cancer: insight of the innate immune system

Front Immunol. 2023 Nov 23:14:1294434. doi: 10.3389/fimmu.2023.1294434. eCollection 2023.

Abstract

Cancer immunotherapies include monoclonal antibodies, cytokines, oncolytic viruses, cellular therapies, and other biological and synthetic immunomodulators. These are traditionally studied for their effect on the immune system's role in eliminating cancer cells. However, some of these therapies have the unique ability to directly induce cytotoxicity in cancer cells by inducing immunogenic cell death (ICD). Unlike general immune stimulation, ICD triggers specific therapy-induced cell death pathways, based on the release of damage-associated molecular patterns (DAMPs) from dying tumour cells. These activate innate pattern recognition receptors (PRRs) and subsequent adaptive immune responses, offering the promise of sustained anticancer drug efficacy and durable antitumour immune memory. Exploring how onco-immunotherapies can trigger ICD, enhances our understanding of their mechanisms and potential for combination strategies. This review explores the complexities of these immunotherapeutic approaches that induce ICD, highlighting their implications for the innate immune system, addressing challenges in cancer treatment, and emphasising the pivotal role of ICD in contemporary cancer research.

Keywords: cellular therapies; cytokines; immunogenic cell death; immunomodulators; innate immune system; monoclonal antibodies; onco-immunotherapy; oncolytic virus.

Publication types

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

MeSH terms

  • Antineoplastic Agents* / therapeutic use
  • Humans
  • Immune System / metabolism
  • Immunogenic Cell Death
  • Immunotherapy
  • Neoplasms* / pathology

Substances

  • Antineoplastic Agents

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. ACMT and KMCR thank CONAHCYT, ANUIES, and ECOSNORD for financial support. DS-A thanks Agence Nationale de recherche sur le Sida, Hépatites Virales et Maladies Infectieuses Émergentes (ANRS-MIE) for financial support.