tetano
Editor, Senior Moderator
Geroscience
. 2026 Mar 20.
doi: 10.1007/s11357-026-02198-8. Online ahead of print.
IFN-β as a therapeutic agent for influenza A virus infection in old mice
Wenxin Wu[SUP] 1 [/SUP], Jeremy S Alexander[SUP] 1 [/SUP], Yang Song[SUP] 1 [/SUP], J Leland Booth[SUP] 1 [/SUP], Alexandra K Ford[SUP] 2 [/SUP], Jordan P Metcalf[SUP] 3 4 5 [/SUP], Douglas A Drevets[SUP] 6 [/SUP]
Affiliations
Background: Age > 65 yrs is a risk factor for poor outcomes to influenza A virus (IAV) infection, due in part to dysregulated interferon (IFN) responses. In some models of IFN dysregulation, IFN-β administration during IAV infection improves survival and antiviral defenses. This study tested whether IFN-β administration to old mice modified disease after IAV infection without accentuating lung or brain damage.
Methods: Young (12-weeks) and old (70-weeks) male C57Bl/6 J mice were inoculated intranasal (i.n.) with 200 PFU H1N1 A/PR/34/8 (PR8) or sterile saline. Old mice received IFN-β (2,000 U) i.n. 1d before and post-infection (p.i). Gene expression in lung and brain was measured by quantitative real time-PCR (qRT-PCR), 3d and 7d p.i. and by nCounts in whole brain, then analyzed with nSolver 4.0 and IPA® software.
Results: IFN-β treated old mice lost significantly less weight than did untreated old mice. IFN-β treatment increased the lung viral load at 3d p.i. without significantly changing the lung/body weight ratio, expression of lung inflammatory mediator genes, or histopathology of lung and brain. In contrast, brain inflammatory genes and pathways were inhibited at 3d p.i. by IFN-β but rebounded by 7d p.i. while damage-associated and some behavioral function pathways remained suppressed. TSPO, TNF, TREM2, and PIAS were possible upstream regulators of altered inflammatory and neurocognitive pathways.
Conclusions: IFN-β administration to IAV-infected old mice improved overall outcome without worsening lung damage and inhibited neuroinflammatory and brain damage-associated pathways. These results suggest IFN-β warrants further investigation as adjunctive treatment for severe viral infections in select hosts.
. 2026 Mar 20.
doi: 10.1007/s11357-026-02198-8. Online ahead of print.
IFN-β as a therapeutic agent for influenza A virus infection in old mice
Wenxin Wu[SUP] 1 [/SUP], Jeremy S Alexander[SUP] 1 [/SUP], Yang Song[SUP] 1 [/SUP], J Leland Booth[SUP] 1 [/SUP], Alexandra K Ford[SUP] 2 [/SUP], Jordan P Metcalf[SUP] 3 4 5 [/SUP], Douglas A Drevets[SUP] 6 [/SUP]
Affiliations
- PMID: 41860731
- DOI: 10.1007/s11357-026-02198-8
Background: Age > 65 yrs is a risk factor for poor outcomes to influenza A virus (IAV) infection, due in part to dysregulated interferon (IFN) responses. In some models of IFN dysregulation, IFN-β administration during IAV infection improves survival and antiviral defenses. This study tested whether IFN-β administration to old mice modified disease after IAV infection without accentuating lung or brain damage.
Methods: Young (12-weeks) and old (70-weeks) male C57Bl/6 J mice were inoculated intranasal (i.n.) with 200 PFU H1N1 A/PR/34/8 (PR8) or sterile saline. Old mice received IFN-β (2,000 U) i.n. 1d before and post-infection (p.i). Gene expression in lung and brain was measured by quantitative real time-PCR (qRT-PCR), 3d and 7d p.i. and by nCounts in whole brain, then analyzed with nSolver 4.0 and IPA® software.
Results: IFN-β treated old mice lost significantly less weight than did untreated old mice. IFN-β treatment increased the lung viral load at 3d p.i. without significantly changing the lung/body weight ratio, expression of lung inflammatory mediator genes, or histopathology of lung and brain. In contrast, brain inflammatory genes and pathways were inhibited at 3d p.i. by IFN-β but rebounded by 7d p.i. while damage-associated and some behavioral function pathways remained suppressed. TSPO, TNF, TREM2, and PIAS were possible upstream regulators of altered inflammatory and neurocognitive pathways.
Conclusions: IFN-β administration to IAV-infected old mice improved overall outcome without worsening lung damage and inhibited neuroinflammatory and brain damage-associated pathways. These results suggest IFN-β warrants further investigation as adjunctive treatment for severe viral infections in select hosts.