Reactive oxygen species-powered cancer immunotherapy: Current status and challenges

J Control Release. 2023 Apr:356:623-648. doi: 10.1016/j.jconrel.2023.02.040. Epub 2023 Mar 21.

Abstract

Reactive oxygen species (ROS) are crucial signaling molecules that can arouse immune system. In recent decades, ROS has emerged as a unique therapeutic strategy for malignant tumors as (i) it can not only directly reduce tumor burden but also trigger immune responses by inducing immunogenic cell death (ICD); and (ii) it can be facilely generated and modulated by radiotherapy, photodynamic therapy, sonodynamic therapy and chemodynamic therapy. The anti-tumor immune responses are, however, mostly downplayed by the immunosuppressive signals and dysfunction of effector immune cells within the tumor microenvironment (TME). The past years have seen fierce developments of various strategies to power ROS-based cancer immunotherapy by e.g. combining with immune checkpoints inhibitors, tumor vaccines, and/or immunoadjuvants, which have shown to potently inhibit primary tumors, metastatic tumors, and tumor relapse with limited immune-related adverse events (irAEs). In this review, we introduce the concept of ROS-powered cancer immunotherapy, highlight the innovative strategies to boost ROS-based cancer immunotherapy, and discuss the challenges in terms of clinical translation and future perspectives.

Keywords: Reactive oxygen species; cancer therapy; cancer vaccines; immune checkpoint inhibitors; immunoadjuvants; immunogenic cell death.

Publication types

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

MeSH terms

  • Adjuvants, Immunologic
  • Cancer Vaccines*
  • Cell Line, Tumor
  • Humans
  • Immunotherapy
  • Neoplasms* / therapy
  • Photochemotherapy*
  • Reactive Oxygen Species
  • Tumor Microenvironment

Substances

  • Reactive Oxygen Species
  • Adjuvants, Immunologic
  • Cancer Vaccines