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Attomolar fecal cytokine profiling reveals gut immune dynamics and disease states

Zhang, S. J.; Sharma, U.; Senussi, Y.; Dayao, A.; Brown, M.; Lomphithak, T.; Nguyen, M.; Lawless, A.; Briskin, C.; Sharova, T.; Boland, G.; Cohen, S.; Snapper, S.; Gazzaniga, F.; Bry, L.; Walt, D.; Gibson, T. E.

2026-04-02 systems biology
10.64898/2026.03.31.714463 bioRxiv
Show abstract

The gut modulates systemic health, influencing immune, neurological, and cardiovascular processes. While fecal sequencing of microbial nucleic acids provides a non-invasive view of microbial composition, sensitive measurement of host-derived signals in stool remains limited. Here we introduce DIGEST (Digital Immunoassay for Gut-Environment Single-molecule Targets), an ultrasensitive digital immunoassay that quantifies proteins in fecal extracts to attomolar levels. In mice, longitudinal profiling during a high-fat diet perturbation revealed coordinated host cytokine responses that occurred within 24 hours, with sustained elevation after diet withdrawal, enabling non-invasive tracking of within-subject immune dynamics. Application of DIGEST to quantify a panel of host inflammatory cytokines in patients with inflammatory bowel disease distinguished active ulcerative colitis from quiescent disease and non-IBD controls (AUC=0.98). In advanced melanoma patients receiving PD-1 blockade, pretreatment fecal IL-23 concentrations discriminated responders from non-responders with an AUC of 0.87. Together, these results establish DIGEST as a generalizable platform for sensitive, non-invasive quantification of host protein activity at the gut interface, with broad applications in basic science discovery, disease surveillance, and therapy response prediction.

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