Polymer-mediated nanoformulations: a promising strategy for cancer immunotherapy

Naunyn Schmiedebergs Arch Pharmacol. 2024 Mar;397(3):1311-1326. doi: 10.1007/s00210-023-02699-9. Epub 2023 Sep 11.

Abstract

Engineering polymer-based nano-systems have attracted many researchers owing to their unique qualities like shape, size, porosity, mechanical strength, biocompatibility, and biodegradability. Both natural and synthetic polymers can be tuned to get desired surface chemistry and functionalization to improve the efficacy of cancer therapy by promoting targeted delivery to the tumor site. Recent advancements in cancer immunoediting have been able to manage both primary tumor and metastatic lesions via activation of the immune system. The combinations of nano-biotechnology and immunotherapeutic agents have provided positive outcomes by enhancing the host immune response in cancer therapy. The nanoparticles have been functionalized using antibodies, targeted antigens, small molecule ligands, and other novel agents that can interact with biological systems at nanoscale levels. Several polymers, such as polyethylene glycol (PEG), poly(lactic-co-glycolic acid) (PLGA), poly(ε-caprolactone) (PCL), and chitosan, have been approved by the Food and Drug Administration for clinical use in biomedicine. The polymeric nanoformulations such as polymers-antibody/antigen conjugates and polymeric drug conjugates are currently being explored as nanomedicines that can target cancer cells directly or target immune cells to promote anti-cancer immunotherapy. In this review, we focus on scientific developments and advancements on engineered polymeric nano-systems in conjugation with immunotherapeutic agents targeting the tumor microenvironment to improve their efficacy and the safety for better clinical outcomes.

Keywords: Antibodies; Immune cells; Immunotherapy; Polymeric nanoparticles; Targeted delivery; Tumor microenvironment.

Publication types

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

MeSH terms

  • Drug Delivery Systems
  • Humans
  • Immunotherapy
  • Nanoparticles* / chemistry
  • Neoplasms* / drug therapy
  • Polyethylene Glycols / chemistry
  • Polymers / chemistry
  • Polymers / therapeutic use
  • Tumor Microenvironment

Substances

  • Polymers
  • Polyethylene Glycols