Autophagy induction by thiostrepton improves the efficacy of immunogenic chemotherapy

J Immunother Cancer. 2020 Mar;8(1):e000462. doi: 10.1136/jitc-2019-000462.

Abstract

Background: Immunogenic cell death (ICD) is a peculiar modality of cellular demise that elicits adaptive immune responses and triggers T cell-dependent immunity.

Methods: Fluorescent biosensors were employed for an unbiased drug screen approach aiming at the identification of ICD enhancers.

Results: Here, we discovered thiostrepton as an enhancer of ICD able to boost chemotherapy-induced ATP release, calreticulin exposure and high-mobility group box 1 exodus. Moreover, thiostrepton enhanced anticancer immune responses of oxaliplatin (OXA) in vivo in immunocompetent mice, yet failed to do so in immunodeficient animals. Consistently, thiostrepton combined with OXA altered the ratio of cytotoxic T lymphocytes to regulatory T cells, thus overcoming immunosuppression and reinstating anticancer immunosurveillance.

Conclusion: Altogether, these results indicate that thiostrepton can be advantageously combined with chemotherapy to enhance anticancer immunogenicity.

Keywords: adaptive immunity; immunomodulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Antineoplastic Agents / pharmacology
  • Autophagy / drug effects
  • Autophagy / immunology
  • Calreticulin / metabolism
  • Cell Line, Tumor
  • Disease Models, Animal
  • Female
  • HMGB1 Protein / metabolism
  • Humans
  • Immunogenic Cell Death
  • Mice
  • Mice, Inbred C57BL
  • Neoplasms / drug therapy*
  • Neoplasms / immunology*
  • Neoplasms / metabolism
  • Oxaliplatin / pharmacology*
  • T-Lymphocytes, Cytotoxic / drug effects
  • T-Lymphocytes, Cytotoxic / immunology*
  • Thiostrepton / pharmacology*

Substances

  • Anti-Bacterial Agents
  • Antineoplastic Agents
  • CALR protein, human
  • Calreticulin
  • HMGB1 Protein
  • Oxaliplatin
  • Thiostrepton