Opportunities and challenges of CD47-targeted therapy in cancer immunotherapy

Oncol Res. 2023 Nov 15;32(1):49-60. doi: 10.32604/or.2023.042383. eCollection 2023.

Abstract

Cancer immunotherapy has emerged as a promising strategy for the treatment of cancer, with the tumor microenvironment (TME) playing a pivotal role in modulating the immune response. CD47, a cell surface protein, has been identified as a crucial regulator of the TME and a potential therapeutic target for cancer therapy. However, the precise functions and implications of CD47 in the TME during immunotherapy for cancer patients remain incompletely understood. This comprehensive review aims to provide an overview of CD47's multifaced role in TME regulation and immune evasion, elucidating its impact on various types of immunotherapy outcomes, including checkpoint inhibitors and CAR T-cell therapy. Notably, CD47-targeted therapies offer a promising avenue for improving cancer treatment outcomes, especially when combined with other immunotherapeutic approaches. The review also discusses current and potential CD47-targeted therapies being explored for cancer treatment and delves into the associated challenges and opportunities inherent in targeting CD47. Despite the demonstrated effectiveness of CD47-targeted therapies, there are potential problems, including unintended effects on healthy cells, hematological toxicities, and the development if resistance. Consequently, further research efforts are warranted to fully understand the underlying mechanisms of resistance and to optimize CD47-targeted therapies through innovative combination approaches, ultimately improving cancer treatment outcomes. Overall, this comprehensive review highlights the significance of CD47 as a promising target for cancer immunotherapy and provides valuable insight into the challenges and opportunities in developing effective CD47-targeted therapies for cancer treatment.

Keywords: CAR T-cell therapy; CD47; CD47-targeted therapies; Cancer cell; Cancer immunotherapy; Cancer treatment outcomes; Checkpoint inhibitors; Immune evasion; Macrophage; Tumor microenvironment.

Publication types

  • Review

MeSH terms

  • CD47 Antigen*
  • Humans
  • Immunotherapy
  • Membrane Proteins
  • Neoplasms* / therapy
  • Tumor Microenvironment

Substances

  • CD47 Antigen
  • Membrane Proteins
  • CD47 protein, human