Mycobacterial Hsp65 antigen delivered by invasive Lactococcus lactis reduces intestinal inflammation and fibrosis in TNBS-induced chronic colitis model

Sci Rep. 2020 Nov 18;10(1):20123. doi: 10.1038/s41598-020-77276-8.

Abstract

Intestinal fibrosis associated with Crohn's disease (CD), which a common and serious complication of inflammatory bowel diseases. In this context, heat shock proteins (HSPs) might serve as an alternative treatment because these antigens play important roles in the regulation of effector T cells. We thus evaluated the anti-inflammatory and antifibrotic capacities of an invasive and Hsp65-producing strain-Lactococcus lactis NCDO2118 FnBPA+ (pXYCYT:Hsp65)-in chronic intestinal inflammation to assess its potential as an alternative therapeutic strategy against fibrotic CD. Experimental colitis was induced by 2,4,6-trinitrobenzene sulfonic acid (TNBS) in BALB/c mice, and the mice were treated orally with L. lactis NCDO2118 FnBPA+ (pXYCYT:Hsp65) via intragastric gavage. The oral administration of this strain significantly attenuated the severity of inflammation and intestinal fibrosis in mice (p < 0.05). These results are mainly justified by reductions in the levels of the pro-fibrotic cytokines IL-13 and TGF-β and increases in the concentration of the regulatory cytokine IL-10. The L. lactis NCDO2118 FnBPA+ (pXYCYT:Hsp65) strain contributed to reductions in the severity of inflammatory damage in chronic experimental CD, and these findings confirm the effectiveness of this new antifibrotic strategy based on the delivery of therapeutic proteins to inside cells of the host intestinal mucosa.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Proteins / administration & dosage
  • Bacterial Proteins / pharmacology*
  • Chaperonin 60 / administration & dosage
  • Chaperonin 60 / pharmacology*
  • Colitis / chemically induced
  • Colitis / drug therapy*
  • Colitis / pathology
  • Cytokines / metabolism
  • Disease Models, Animal
  • Female
  • Fibrosis / drug therapy
  • Fibrosis / pathology
  • Immunoglobulin A / metabolism
  • Lactococcus lactis / genetics*
  • Mice, Inbred BALB C
  • Microorganisms, Genetically-Modified
  • Trinitrobenzenesulfonic Acid / toxicity

Substances

  • Bacterial Proteins
  • Chaperonin 60
  • Cytokines
  • Immunoglobulin A
  • heat-shock protein 65, Mycobacterium
  • Trinitrobenzenesulfonic Acid