Trained ILC3 responses promote intestinal defense

Author:

Serafini Nicolas1ORCID,Jarade Angélique1ORCID,Surace Laura1ORCID,Goncalves Pedro1ORCID,Sismeiro Odile2ORCID,Varet Hugo23ORCID,Legendre Rachel23ORCID,Coppee Jean-Yves2,Disson Olivier4ORCID,Durum Scott K.5,Frankel Gad6ORCID,Di Santo James P.1ORCID

Affiliation:

1. Institut Pasteur, Université de Paris, Inserm U1223, Innate Immunity Unit, Paris, France.

2. Institut Pasteur, Université de Paris, Transcriptome and Epigenome Platform–Biomics Pole, Paris, France.

3. Institut Pasteur, Université de Paris, Bioinformatics and Biostatistics Hub, Paris, France.

4. Institut Pasteur, Université de Paris, Inserm U1117, Biology of Infection Unit, Paris, France.

5. Laboratory of Cancer and Immunometabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD, USA.

6. MRC Centre for Molecular Bacteriology and Infection, Department of Life Sciences, Imperial College London, London, UK.

Abstract

Group 3 innate lymphoid cells (ILC3s) are innate immune effectors that contribute to host defense. Whether ILC3 functions are stably modified after pathogen encounter is unknown. Here, we assess the impact of a time-restricted enterobacterial challenge to long-term ILC3 activation in mice. We found that intestinal ILC3s persist for months in an activated state after exposure to Citrobacter rodentium . Upon rechallenge, these “trained” ILC3s proliferate, display enhanced interleukin-22 (IL-22) responses, and have a superior capacity to control infection compared with naïve ILC3s. Metabolic changes occur in C. rodentium –exposed ILC3s, but only trained ILC3s have an enhanced proliferative capacity that contributes to increased IL-22 production. Accordingly, a limited encounter with a pathogen can promote durable phenotypic and functional changes in intestinal ILC3s that contribute to long-term mucosal defense.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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