Targeting glioblastoma through nano- and micro-particle-mediated immune modulation

Bioorg Med Chem. 2022 Oct 15:72:116913. doi: 10.1016/j.bmc.2022.116913. Epub 2022 Jul 8.

Abstract

Glioblastoma Multiforme (GBM) is a multifaceted and complex disease, which has experienced no changes in treatment for nearly two decades and has a 5-year survival rate of only 5.4%. Alongside challenges in delivering chemotherapeutic agents across the blood brain barrier (BBB) to the tumour, the immune microenvironment is also heavily influenced by tumour signalling. Immunosuppression is a major aspect of GBM; however, evidence remains conflicted as to whether pro-inflammatory or anti-inflammatory therapies are the key to improving GBM treatment. To address both of these issues, particle delivery systems can be designed to overcome BBB transport while delivering a wide variety of immune-stimulatory molecules to investigate their effect on GBM. This review explores literature from the past 3 years that combines particle delivery systems alongside immunotherapy for the effective treatment of GBM.

Keywords: Blood brain barrier; Cytokines and cell signalling; Glioblastoma multiforme; Hyperthermal therapy; Immune checkpoint inhibitor; Particle delivery; T regulatory cells; Temozolomide; Tumour-associated macrophages; short interfering RNA (siRNA).

Publication types

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

MeSH terms

  • Antineoplastic Agents* / therapeutic use
  • Blood-Brain Barrier
  • Brain Neoplasms* / drug therapy
  • Glioblastoma* / drug therapy
  • Humans
  • Immunotherapy
  • Tumor Microenvironment

Substances

  • Antineoplastic Agents