AI Article Synopsis

  • Interleukin-7 (IL-7) plays a crucial role in the development of B- and T-lymphocytes and has been identified as a key survival factor for certain innate T cells important in antibacterial immunity.
  • *Research shows that delivering IL-7 topically can enhance the number of RORγt IL-17A-producing innate T cells, leading to improved bacterial control during infections like those caused by Streptococcus pneumoniae.
  • *Combining IL-7 treatment with α-galactosylceramide can significantly increase survival rates during infections by boosting IL-17 production and neutrophil response, suggesting IL-7 could be a potential new treatment for bacterial infections.*

Article Abstract

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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Source
http://dx.doi.org/10.1038/s41385-019-0212-yDOI Listing

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