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J Clin Invest . Effect of external cues on clock-driven protection from influenza A infection

tetano

Editor, Senior Moderator
J Clin Invest


. 2025 Nov 17;135(22):e193133.
doi: 10.1172/JCI193133. Effect of external cues on clock-driven protection from influenza A infection

Oindrila Paul[SUP] 1 [/SUP], Thomas G Brooks[SUP] 2 [/SUP], Alisha Shetty[SUP] 1 [/SUP], Y Jane Choi[SUP] 1 [/SUP], Martina Towers[SUP] 1 [/SUP], Lora J Assi[SUP] 1 [/SUP], James P Garifallou[SUP] 1 [/SUP], Kaitlyn Forrest[SUP] 1 [/SUP], Alecia Cameron[SUP] 1 [/SUP], Amita Sehgal[SUP] 2 3 [/SUP], Gregory Grant[SUP] 4 [/SUP], Shaon Sengupta[SUP] 1 2 5 [/SUP]



Affiliations
Free article Abstract

Influenza and other respiratory viral pathogens remain leading causes of mortality and morbidity. Circadian rhythms play a critical role in regulating immune responses and can confer temporal protection from influenza infection. Here, we investigated whether this protection requires rhythmic function after the initial infection by manipulating environmental cycles. We found that disrupting environmental lighting cues within a critical window of vulnerability abrogated the time-of-day-specific protection. This poor outcome was mediated by a dysregulated immune response, as evidenced by the accumulation of inflammatory monocytes and CD8+ T cells in the lungs and a transcriptomic profile indicative of an exaggerated inflammation. Disruption of the light cycle did not affect outcomes in a clock mutant, indicating that it acts through the host's circadian clock. Importantly, rhythmic meal timing mitigated the adverse effects of disrupted light cycles, supporting the idea that external cues acting through different body clocks can compensate for one another. Together, these findings underscore the critical interplay between environmental timing cues and endogenous circadian rhythms in determining influenza outcomes and offer translational insight into optimizing care for critically ill patients with respiratory viral infections.

Keywords: Immunology; Inflammation; Influenza; Innate immunity; Pulmonology; T cells.

 
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