Nanoparticle-Mediated Delivery of Inhaled Immunotherapeutics for Treating Lung Metastasis

Adv Mater. 2021 Feb;33(7):e2007557. doi: 10.1002/adma.202007557. Epub 2021 Jan 14.

Abstract

Despite the critical breakthrough achieved by immune checkpoint blockade (ICB), the clinical benefits are usually restricted by inefficient infiltration of immune cells and immune-associated adverse effects. Noninvasive aerosol inhalation, as a definitive procedure for treatment of respiratory diseases, for ICB immunotherapy against lung metastasis, has not been realized to the best knowledge. Herein, an inhaled immunotherapeutic chitosan (CS)-antibody complex is developed for immunotherapy against lung cancer. In this system, CS is used as a carrier to assemble with anti-programmed cell death protein ligand 1 (aPD-L1) to enable efficient transmucosal delivery. Moreover, CS exhibits adjuvant effects to drive potent immune responses via activating the cyclic-di-GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) pathway. Interestingly, repeated inhalation of CS/aPD-L1 complex can effectively activate the immune system by promoting the infiltration of different immune cells especially CD8+ T cells around tumor lesions, and finally prolongs the survival of mice to 60 days. Thus, the work presents a unique aerosol inhalation delivery system for ICB antibody, which is promising for immunotherapy against lung metastasis without the concern of systemic toxicity.

Keywords: cancer immunotherapy; immune checkpoint blockade; inhalation; lung cancer; pulmonary drug delivery.

MeSH terms

  • Administration, Inhalation
  • Animals
  • Antibodies, Monoclonal, Humanized / chemistry*
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / immunology
  • Biological Transport
  • CD8-Positive T-Lymphocytes / metabolism
  • Chitosan / chemistry*
  • Drug Liberation
  • Female
  • Humans
  • Immune Checkpoint Inhibitors / chemistry*
  • Immune Checkpoint Inhibitors / metabolism
  • Immunotherapy
  • Lung Neoplasms / immunology*
  • Lung Neoplasms / therapy
  • Mice
  • Mice, Inbred C57BL
  • Mucins / chemistry
  • Mucins / metabolism
  • N-Acetylneuraminic Acid / chemistry
  • N-Acetylneuraminic Acid / metabolism
  • Nanocapsules / chemistry*
  • Protein Multimerization
  • Signal Transduction

Substances

  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents
  • Immune Checkpoint Inhibitors
  • Mucins
  • Nanocapsules
  • atezolizumab
  • Chitosan
  • N-Acetylneuraminic Acid