Multifunctional nanoparticles for cancer immunotherapy: A groundbreaking approach for reprogramming malfunctioned tumor environment

J Control Release. 2018 Mar 28:274:24-34. doi: 10.1016/j.jconrel.2018.01.028. Epub 2018 Jan 31.

Abstract

Several cancer immunotherapy approaches have been recently introduced into the clinics and they have shown remarkable therapeutic potentials. The groundbreaking cancer immunotherapeutic agents function as a stimulant or modulator of the body immune system to fight against or kill cancers. Although targeted immunotherapies such as immune check point inhibitors (CTLA-4 or PD-1/PD-L1), DNA vaccination and CAR-T therapy are revolutionizing cancer treatment, the delivery efficacy can be further improved while their off-target toxicity can be mitigated through nanotechnology approaches. Recent research has demonstrated that nanotechnology has multifaceted role for (i) reeducating tumor associated macrophages (TAM) to function as tumor suppressor agent, (ii) serving as an efficient alternative for Chimeric Antigen Receptor (CAR)-T cell generation and transduction, and (iii) selective knockdown of Kras oncogene addiction by nano-Crisper-Cas9 delivery system. The function of host immune stimulatory signals and tumor immunotherapies can further be improved by repurposing of nanomedicine platform. This review summarizes the role of multifunctional polymeric, lipid, metallic and cell based nanoparticles for improving current immunotherapy.

Keywords: CAR-T; CRISPR-Cas9; CTLA-4 targeting; Cancer; Cytokine storm; Dendritic cell vaccine; Immunotherapy; Nanomedicine; PD-1/PDL-1 targeting; Tumor associated macrophages.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antineoplastic Agents* / administration & dosage
  • Antineoplastic Agents* / therapeutic use
  • B7-H1 Antigen / antagonists & inhibitors
  • CRISPR-Associated Protein 9
  • CTLA-4 Antigen / antagonists & inhibitors
  • Cancer Vaccines / therapeutic use
  • Humans
  • Immunotherapy* / methods
  • Nanomedicine / methods
  • Nanoparticles*
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • Receptors, Antigen, T-Cell / immunology
  • Vaccines, DNA / therapeutic use

Substances

  • Antineoplastic Agents
  • B7-H1 Antigen
  • CD274 protein, human
  • CTLA-4 Antigen
  • CTLA4 protein, human
  • Cancer Vaccines
  • Receptors, Antigen, T-Cell
  • Vaccines, DNA
  • CRISPR-Associated Protein 9