The Love-Hate Relationship Between TGF-β Signaling and the Immune System During Development and Tumorigenesis

Front Immunol. 2022 May 26:13:891268. doi: 10.3389/fimmu.2022.891268. eCollection 2022.

Abstract

Since TGF-β was recognized as an essential secreted cytokine in embryogenesis and adult tissue homeostasis a decade ago, our knowledge of the role of TGF-β in mammalian development and disease, particularly cancer, has constantly been updated. Mounting evidence has confirmed that TGF-β is the principal regulator of the immune system, as deprivation of TGF-β signaling completely abrogates adaptive immunity. However, enhancing TGF-β signaling constrains the immune response through multiple mechanisms, including boosting Treg cell differentiation and inducing CD8+ T-cell apoptosis in the disease context. The love-hate relationship between TGF-β signaling and the immune system makes it challenging to develop effective monotherapies targeting TGF-β, especially for cancer treatment. Nonetheless, recent work on combination therapies of TGF-β inhibition and immunotherapy have provide insights into the development of TGF-β-targeted therapies, with favorable outcomes in patients with advanced cancer. Hence, we summarize the entanglement between TGF-β and the immune system in the developmental and tumor contexts and recent progress on hijacking crucial TGF-β signaling pathways as an emerging area of cancer therapy.

Keywords: TGF-β; cancer therapy; immune system; tumor microenvironment; tumor progression.

Publication types

  • Review

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / metabolism
  • Carcinogenesis / immunology
  • Cell Transformation, Neoplastic
  • Humans
  • Immunotherapy
  • Neoplasms* / immunology
  • Neoplasms* / pathology
  • Neoplasms* / therapy
  • Signal Transduction / immunology
  • Transforming Growth Factor beta* / immunology
  • Transforming Growth Factor beta* / metabolism

Substances

  • Transforming Growth Factor beta