Modulation of Th17 and regulatory T‐cell responses during murine pregnancy contributes to increased maternal susceptibility to Salmonella Typhimurium infection. (9th October 2017)

• Record Type: Journal Article
• Authors: Agbayani, Gerard; Wachholz, Kristina; Chattopadhyay, Anindita; Gurnani, Komal; Murphy, Shawn P.; Krishnan, Lakshmi
• Is Part Of: American journal of reproductive immunology. Volume 78:Number 6(2017)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2017-10-09
• Subjects: cytokines -- pregnancy -- regulatory T cells -- Salmonella -- Th17 -- TLR 4; Human reproduction -- Immunological aspects -- Periodicals; 616.69206
• DOI: 10.1111/aji.12742
• Languages: English
• ISSNs: 1046-7408

Abstract

Abstract : Problem: Salmonella Typhimurium ( S . Tm) infection in pregnant mice results in massive placental infection, fetal loss, and exacerbated systemic infection. The Th17 host response can aid control of S . Tm infection, whereas successful pregnancy correlates to a dampened inflammatory and enhanced regulatory T‐cell (Treg) response. Method of study: Mice were infected systemically with S . Tm and tissue bacterial burden, splenic Th17 and Treg cell numbers, and serum cytokines were analyzed. Splenic and/or placental mRNA expression of IL‐17A, RORγ‐t, IL‐10, and TNF was determined. The effects of in vivo CD25 + cell depletion and TLR4 blockade on the course of S . Tm infection and Th17 response were determined. Results: Enhanced S . Tm burden in pregnant mice was associated with time‐dependent increased serum inflammatory cytokines. In vivo, TLR4 blockade reduced splenic S . Tm burden, suggesting detrimental TLR4‐mediated inflammation. However, the splenic and placental Th17 response was reduced in S . Tm‐infected pregnant mice relative to non‐pregnant controls. Alternatively, there was an increase in splenic Treg frequency in pregnant mice and depletion of this subset reduced bacterial burden and increased the Th17 response. Conclusion: Downregulation of Th17 cell responses by Tregs during pregnancy potentially contributes to exacerbation of S . Tm infection in pregnant mice. Abstract :