Interleukin-7 protects against bacterial respiratory infection by promoting IL-17A-producing innate T-cell response

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Hassane, Maya | Jouan, Youenn | Creusat, Florent | Soulard, Daphnée | Boisseau, Chloé | Gonzalez, Loïc | Patin, Emmanuel C | Heuzé-Vourc'H, Nathalie | Sirard, J.‐c. | Faveeuw, Christelle | Trottein, François | Si-Tahar, Mustapha | Baranek, Thomas | Paget, Christophe

Edité par CCSD ; Nature Pub. Group -

International audience. Interleukin-7 (IL-7) is a critical cytokine in B- and T-lymphocyte development and maturation. Recent evidence suggests that IL-7 is a preferential homeostatic and survival factor for RORγt+ innate T cells such as natural killer T (NKT) cells, γδT cells, and mucosal-associated invariant T (MAIT) cells in the periphery. Given the important contribution of these populations in antibacterial immunity at barrier sites, we questioned whether IL-7 could be instrumental in boosting the local host immune response against respiratory bacterial infection. By using a cytokine-monoclonal antibody approach, we illustrated a role for topical IL-7 delivery in increasing the pool of RORγt+ IL-17A-producing innate T cells. Prophylactic IL-7 treatment prior to Streptococcus pneumoniae infection led to better bacterial containment, a process associated with increased neutrophilia and that depended on γδT cells and IL-17A. Last, combined delivery of IL-7 and α-galactosylceramide (α-GalCer), a potent agonist for invariant NKT (iNKT) cells, conferred an almost total protection in terms of survival, an effect associated with enhanced IL-17 production by innate T cells and neutrophilia. Collectively, we provide a proof of concept that IL-7 enables fine-tuning of innate T- cell functions. This might pave the way for considering IL-7 as an innovative biotherapeutic against bacterial infection.

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