ReviewFrontiers in immunology2025
The Role of SR-BI in sepsis: leveraging mechanistic insights to advance precision steroid therapy.
Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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
2 citing papers in PubMed.
- Identification of scavenger receptor BI as a scavenger of free heme that is essential for protection against hemolysis.Nature communications · 2026Article
- Different Functions of Human Scavenger Receptors BI and BII Overexpressed in a Murine Abdominal Sepsis Model.Biomolecules · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
According to the Surviving Sepsis Campaign, 50.3% of septic shock patients received steroid/glucocorticoid (GC) therapy. However, whether GC therapy is beneficial and who might benefit from it are hotly debated. Initial guidelines recommended GC therapy for septic patients with adrenal insufficiency, but this has since been retracted. Recent studies using animal models of adrenal insufficiency have shed light on the mechanisms, demonstrating that the adrenal stress response is a part of the host response that is essential for control inflammatory response in sepsis and the adrenal insufficiency is a risk factor for sepsis. This perspective review explores the limitations of GC therapy through the lens of GC biology, with a particular focus on the role of scavenger receptor class B type I (SR-BI) in mediating the adrenal stress response. We highlight the mechanisms of how SR-BI-mediated adrenal stress response contributes to the regulation of hyperinflammation and innate immune responses. By integrating mechanistic insights with the limitations of GC therapy, we advocate for a precision medicine approach to GC therapy in sepsis- selectively applying GC therapy for patients with adrenal insufficiency, not without.
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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 Socratic graph.