A subunit vaccine based on rH-NS induces protection against Mycobacterium tuberculosis infection by inducing the Th1 immune response and activating macrophages

Acta Biochim Biophys Sin (Shanghai). 2016 Oct;48(10):909-922. doi: 10.1093/abbs/gmw078. Epub 2016 Aug 25.

Abstract

Mycobacterium tuberculosis (Mtb) is a Gram-positive pathogen which causes tuberculosis in both animals and humans. All tested rH-NS formulations induced a specific Th1 response, as indicated by increased production of interferon γ (IFN-γ) and interleukin 2 (IL-2) by lymphocytes in the spleen of mice which were immunized with rH-NS alone or with rH-NS and the adjuvant cyclic GMP-AMP (cGAMP). Serum from mice immunized with rH-NS with or without adjuvant also had higher levels of IL-12p40 and TNF-α, compared with those from control mice immunized with phosphate-buffered saline. Both vaccines increased protective efficacy in mice which were challenged with Mtb H37Rv, as measured by reduced relative CFU counts in the lungs. We found that rH-NS induced the production of TNF-α, IL-6, and IL-12p40, which relied on the activation of mitogen-activated protein kinases by stimulating the rapid phosphorylation of ERK1/2, p38, and JNK, and on the activation of transcription factor NF-κB in macrophages. Additionally, we also found that rH-NS could interact with TLR2 but not TLR4 in pull-down assays. The rH-NS-induced cytokine production from TLR2-silenced RAW264.7 cells was lower than that from BALB/c macrophages. Prolonged exposure (>24 h) of RAW264.7 cells to rH-NS resulted in a significant enhancement in IFN-γ-induced MHC II expression, which was not found in shTLR2-treated RAW264.7 cells. These results suggest that rH-NS is a TLR2 agonist which induces the production of cytokines by macrophages and up-regulates macrophage function.

Keywords: APC function; TLR2; adjuvant; cytokines; rH-NS antigen; tuberculosis; vaccines.

MeSH terms

  • Animals
  • Bacterial Proteins / genetics
  • Bacterial Proteins / immunology*
  • Bacterial Vaccines / genetics
  • Bacterial Vaccines / immunology*
  • Blotting, Western
  • Cell Line
  • Cytokines / genetics
  • Cytokines / immunology
  • Cytokines / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / immunology*
  • HEK293 Cells
  • Host-Pathogen Interactions / immunology
  • Humans
  • Immunization / methods
  • Macrophage Activation / immunology
  • Macrophages / immunology*
  • Macrophages / metabolism
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Mitogen-Activated Protein Kinases / immunology
  • Mitogen-Activated Protein Kinases / metabolism
  • Mycobacterium tuberculosis / immunology*
  • Mycobacterium tuberculosis / physiology
  • Phosphorylation / immunology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Th1 Cells / immunology*
  • Th1 Cells / metabolism
  • Toll-Like Receptor 2 / genetics
  • Toll-Like Receptor 2 / immunology
  • Toll-Like Receptor 2 / metabolism
  • Tuberculosis / immunology*
  • Tuberculosis / microbiology
  • Vaccines, Subunit / genetics
  • Vaccines, Subunit / immunology

Substances

  • Bacterial Proteins
  • Bacterial Vaccines
  • Cytokines
  • DNA-Binding Proteins
  • H-NS protein, bacteria
  • Tlr2 protein, mouse
  • Toll-Like Receptor 2
  • Vaccines, Subunit
  • Mitogen-Activated Protein Kinases