ArticleiScience2026
Cellular immunology data enable clinical severity prediction via supervised machine learning.
Article in iScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
14 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
High-dimensional flow cytometry provides rich immunological data for examining immune responses and their relationships with disease pathology, but its complexity, heterogeneity, high-dimensionality, and modest sample sizes limit translation into clinical applications. We describe a translational immune health framework that applies supervised learning algorithms to integrate high-dimensional cellular immunology data with clinical outcomes. Using COVID-19 as a clinical scenario, we applied this framework to deep immune profiles from patients to classify disease severity and predict future severity changes from baseline profiles. We built predictive models with five supervised algorithms and interpreted associations between immune features and severity outcomes with SHapley Additive exPlanations. This approach identified immune features contributing to severity predictions and provided interpretable links between cellular immune profiles and clinical outcomes. Our findings support machine learning as a practical strategy for analyzing complex immunological data and advancing predictive modeling in translational immune health.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.