Inhibition of PD-1 Protects against TNBS-Induced Colitis via Alteration of Enteric Microbiota

Biomed Res Int. 2021 Jan 7:2021:4192451. doi: 10.1155/2021/4192451. eCollection 2021.

Abstract

Methods: Colitis was induced in mice using 2,4,6-trinitrobenzene-sulfonic acid (TNBS), and mice were subsequently treated with either a PD-1 inhibitor or 5-amino-salicylic acid (ASA) as a positive control. Body weight, disease activity index (DAI), colon length, and tissue damage were evaluated, and the enteric microbiota was profiled using high-throughput 16S rRNA sequencing of fecal samples from the experimental mice.

Results: TNBS caused mice to experience IBD-like symptoms, which were attenuated by the PD-1 inhibitor, as indicated by a decrease in DAI scores (p = 0.0002). Furthermore, in this mouse model of IBD, PD-1 inhibition improved the alpha diversity as well as restored the beta diversity of the enteric microbiome. It also significantly enriched the abundance of short-chain fatty acid- (SCFA-) producing bacteria of the Firmicutes (p < 0.05) and Bacteroidetes (p < 0.05) phyla but depopulated Proteobacteria (p < 0.05).

Conclusion: PD-1 inhibition can partly mitigate TNBS-induced colitis and restore the enteric microbiota by enriching the abundance of SCFA-producing bacteria.

MeSH terms

  • Animals
  • Colitis / chemically induced
  • Colitis / metabolism*
  • Colitis / microbiology*
  • Colon / drug effects
  • Colon / pathology
  • Disease Models, Animal
  • Gastrointestinal Microbiome / drug effects*
  • Immune Checkpoint Inhibitors / pharmacology
  • Male
  • Mesalamine / pharmacology
  • Mice
  • Mice, Inbred BALB C
  • Programmed Cell Death 1 Receptor / antagonists & inhibitors*
  • Protective Agents / pharmacology*
  • Trinitrobenzenesulfonic Acid / adverse effects

Substances

  • Immune Checkpoint Inhibitors
  • Pdcd1 protein, mouse
  • Programmed Cell Death 1 Receptor
  • Protective Agents
  • Mesalamine
  • Trinitrobenzenesulfonic Acid