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Enhancing mucosal immunity by transient microbiota depletion

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...

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Detalles Bibliográficos
Autores principales: Becattini, Simone, Littmann, Eric R., Seok, Ruth, Amoretti, Luigi, Fontana, Emily, Wright, Roberta, Gjonbalaj, Mergim, Leiner, Ingrid M., Plitas, George, Hohl, Tobias M., Pamer, Eric G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7479140/
https://www.ncbi.nlm.nih.gov/pubmed/32901029
http://dx.doi.org/10.1038/s41467-020-18248-4
Descripción
Sumario: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.