Ultrasound nanodroplets loaded with Siglec-G siRNA and Fe3O4 activate macrophages and enhance phagocytosis for immunotherapy of triple-negative breast cancer

J Nanobiotechnology. 2024 Dec 19;22(1):773. doi: 10.1186/s12951-024-03051-w.

Abstract

Background: The progression of triple-negative breast cancer is shaped by both tumor cells and the surrounding tumor microenvironment (TME). Within the TME, tumor-associated macrophages (TAMs) represent a significant cell population and have emerged as a primary target for cancer therapy. As antigen-presenting cells within the innate immune system, macrophages are pivotal in tumor immunotherapy through their phagocytic functions. Due to the highly dynamic and heterogeneous nature of TAMs, re-polarizing them to the anti-tumor M1 phenotype can amplify anti-tumor effects and help mitigate the immunosuppressive TME.

Results: In this study, we designed and constructed an ultrasound-responsive targeted nanodrug delivery system to deliver Siglec-G siRNA and Fe3O4, with perfluorohexane (PFH) at the core and mannose modified on the surface (referred to as MPFS@NDs). Siglec-G siRNA blocks the CD24/Siglec-G mediated "don't eat me" phagocytosis inhibition pathway, activating macrophages, enhancing their phagocytic function, and improving antigen presentation, subsequently triggering anti-tumor immune responses. Fe3O4 repolarizes M2-TAMs to the anti-tumor M1 phenotype. Together, these components synergistically alleviate the immunosuppressive TME, and promote T cell activation, proliferation, and recruitment to tumor tissues, effectively inhibiting the growth of primary tumors and lung metastasis.

Conclusion: This work suggests that activating macrophages and enhancing phagocytosis to remodel the TME could be an effective strategy for macrophage-based triple-negative breast cancer immunotherapy.

Keywords: CD24/Siglec-G; Fe3O4; Immunotherapy; Macrophages; Triple-negative breast cancer.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Female
  • Fluorocarbons / chemistry
  • Humans
  • Immunotherapy* / methods
  • Lectins / chemistry
  • Macrophage Activation / drug effects
  • Macrophages* / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Nanoparticles / chemistry
  • Phagocytosis*
  • RNA, Small Interfering* / chemistry
  • Triple Negative Breast Neoplasms* / therapy
  • Tumor Microenvironment* / drug effects
  • Tumor-Associated Macrophages / immunology

Substances

  • RNA, Small Interfering
  • Fluorocarbons
  • perflexane
  • Lectins