Biocompatible chitosan nanoparticles as an efficient delivery vehicle for Mycobacterium tuberculosis lipids to induce potent cytokines and antibody response through activation of γδ T cells in mice

Nanotechnology. 2017 Apr 21;28(16):165101. doi: 10.1088/1361-6528/aa60fd. Epub 2017 Feb 16.

Abstract

The activation of cell-mediated and humoral immune responses to Mycobacterium tuberculosis (Mtb) is critical for protection against the pathogen and nanoparticle-mediated delivery of antigens is a more potent way to induce different immune responses. Herein, we show that mice immunized with Mtb lipid-bound chitosan nanoparticles (NPs) induce secretion of prominent type-1 T-helper (Th-1) and type-2 T-helper (Th-2) cytokines in lymph node and spleen cells, and also induces significantly higher levels of IgG, IgG1, IgG2 and IgM in comparison to control mice. Furthermore, significantly enhanced γδ-T-cell activation was observed in lymph node cells isolated from mice immunized with Mtb lipid-coated chitosan NPs as compared to mice immunized with chitosan NPs alone or Mtb lipid liposomes. In comparison to CD8+ cells, significantly higher numbers of CD4+ cells were present in both the lymph node and spleen cells isolated from mice immunized with Mtb lipid-coated chitosan NPs. In conclusion, this study represents a promising new strategy for the efficient delivery of Mtb lipids using chitosan NPs to trigger an enhanced cell-mediated and antibody response against Mtb lipids.

MeSH terms

  • Animals
  • Biocompatible Materials
  • Chitosan / chemistry
  • Cytokines / metabolism*
  • Endocytosis / physiology
  • Female
  • Humans
  • Immunity, Humoral / immunology
  • Immunoglobulin G / blood
  • Immunoglobulin M / blood
  • Intraepithelial Lymphocytes / drug effects
  • Intraepithelial Lymphocytes / immunology*
  • Lipids / administration & dosage*
  • Macrophages, Peritoneal / drug effects
  • Mice, Inbred BALB C
  • Mycobacterium tuberculosis / chemistry*
  • Nanoparticles / administration & dosage*
  • Nanoparticles / chemistry
  • Tuberculosis, Pulmonary / drug therapy
  • Tuberculosis, Pulmonary / immunology

Substances

  • Biocompatible Materials
  • Cytokines
  • Immunoglobulin G
  • Immunoglobulin M
  • Lipids
  • Chitosan