ReviewRMD open2026
Emerging treatments for Sjögren's disease: promising drugs on the horizon.
Review in RMD open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
- Translational PBPK Modeling and Exposure-Response Analysis of AT-RvD1 for Treating Sjögren's Disease.Clinical and translational science · 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
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Sjögren's disease (SjD) is a chronic, multisystem autoimmune disorder characterised by lymphocytic infiltration of exocrine glands, leading to dryness, fatigue and variable extraglandular involvement. Despite its significant clinical and socioeconomic burden, no disease-modifying therapies have yet been approved. Current management remains largely symptomatic, reflecting the complexity and heterogeneity of the disease and the limitations of past clinical trials. Recent advances in the understanding of SjD immunopathogenesis have clarified key mechanisms including epithelial activation, interferon-driven inflammation, B-cell hyperactivity and T-cell dysregulation. These insights have fuelled the development of targeted therapies designed to modulate specific immune pathways, aiming to interrupt the self-perpetuating cycle of epithelial injury and immune activation. Emerging strategies include the modulation of B-cell survival and signalling, inhibition of IgG recycling and intracellular kinase pathways and blockade of co-stimulatory interactions between immune cells. Although recent phase II and phase III studies have shown encouraging signs of efficacy, they have largely focused on patients with moderate-to-severe systemic disease. Addressing the unmet therapeutic need in individuals with predominantly glandular or low systemic activity remains a major challenge. Continued refinement of outcome measures and patient stratification will be essential to translate mechanistic advances into effective, personalised treatments capable of altering the natural course of SjD.
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.