Enhancing mucosal immunity by transient microbiota depletion

Nat Commun. 2020 Sep 8;11(1):4475. doi: 10.1038/s41467-020-18248-4.

Abstract

Tissue resident memory CD8+ T cells (Trm) are poised for immediate reactivation at sites of pathogen entry and provide optimal protection of mucosal surfaces. The intestinal tract represents a portal of entry for many infectious agents; however, to date specific strategies to enhance Trm responses at this site are lacking. Here, we present TMDI (Transient Microbiota Depletion-boosted Immunization), an approach that leverages antibiotic treatment to temporarily restrain microbiota-mediated colonization resistance, and favor intestinal expansion to high densities of an orally-delivered Listeria monocytogenes strain carrying an antigen of choice. By augmenting the local chemotactic gradient as well as the antigenic load, this procedure generates a highly expanded pool of functional, antigen-specific intestinal Trm, ultimately enhancing protection against infectious re-challenge in mice. We propose that TMDI is a useful model to dissect the requirements for optimal Trm responses in the intestine, and also a potential platform to devise novel mucosal vaccination approaches.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Animals
  • Antigens / administration & dosage
  • CD8-Positive T-Lymphocytes / immunology
  • Chemotaxis / immunology
  • Female
  • Gastrointestinal Microbiome / drug effects
  • Gastrointestinal Microbiome / immunology*
  • Host Microbial Interactions / immunology
  • Immunity, Mucosal* / drug effects
  • Immunologic Memory
  • Listeria monocytogenes / growth & development
  • Listeria monocytogenes / immunology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Ovalbumin / administration & dosage
  • Streptomycin / administration & dosage

Substances

  • Antigens
  • Ovalbumin
  • Streptomycin