Emerging roles of the gut microbiota in cancer immunotherapy

Front Immunol. 2023 Feb 22:14:1139821. doi: 10.3389/fimmu.2023.1139821. eCollection 2023.

Abstract

Gut microbiota represents a hidden treasure vault encompassing trillions of microorganisms that inhabit the intestinal epithelial barrier of the host. In the past decade, numerous in-vitro, animal and clinical studies have revealed the profound roles of gut microbiota in maintaining the homeostasis of various physiological functions, especially immune modulation, and remarkable differences in the configuration of microbial communities between cancers and healthy individuals. In addition, although considerable efforts have been devoted to cancer treatments, there remain many patients succumb to their disease with the incremental cancer burden worldwide. Nevertheless, compared with the stability of human genome, the plasticity of gut microbiota renders it a promising opportunity for individualized treatment. Meanwhile, burgeoning findings indicate that gut microbiota is involved in close interactions with the outcomes of diverse cancer immunotherapy protocols, including immune checkpoint blockade therapy, allogeneic hematopoietic stem cell transplantation, and chimeric antigen receptor T cell therapy. Here, we reviewed the evidence for the capacity of gut microflora to modulate cancer immunotherapies, and highlighted the opportunities of microbiota-based prognostic prediction, as well as microbiotherapy by targeting the microflora to potentiate anticancer efficacy while attenuating toxicity, which will be pivotal to the development of personalized cancer treatment strategies.

Keywords: Gut microbiota; allogeneic hematopoietic stem cell transplantation; chimeric antigen receptor T cell therapy; immune checkpoint blockade; immunotherapy.

Publication types

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

MeSH terms

  • Animals
  • Gastrointestinal Microbiome*
  • Humans
  • Immunotherapy / methods
  • Intestines / physiology
  • Microbiota* / physiology
  • Neoplasms*

Grants and funding

This work was supported by the Funds for Creative Research Groups of the First Affiliated Hospital of Zhengzhou university (QNCXTD2023012) and the National Natural Science Foundation of China (81970184; 82170183; U1904139; 82070209).