ReviewStem cell research & therapy2026
Mesenchymal stromal cell therapy for systemic lupus erythematosus: mechanisms, clinical translation, and future directions.
Review in Stem cell research & therapy, 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.
- Targeted co-delivery of curcumin and TRAIL via engineered extracellular vesicles: a synergistic therapy against resistant cancers.Drug delivery and translational research · 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
9 authors.
Funding
Abstract
Systemic Lupus Erythematosus (SLE) is a complex autoimmune condition, fundamentally characterized by the loss of self-tolerance. This breakdown leads to the generation of autoantibodies and widespread inflammation that compromises multiple organs. A significant clinical challenge in SLE management is the lack of effective options for refractory disease, driving the pursuit of innovative treatments. Among these, mesenchymal stromal/stem cells (MSCs) have garnered significant attention due to their potent immunomodulatory and tissue-repair capabilities, highlighting their potential as a viable therapy. This review critically assesses the potential of MSCs in reconciling the unmet need for effective SLE therapies by examining their immunomodulatory mechanisms, clinical efficacy, and safety. MSCs reestablish immune tolerance through coordinated interactions with T and B cells, macrophages, and dendritic cells, predominantly facilitated by soluble factor secretion and extracellular vesicle release. In severe SLE, allogeneic MSC transplantation has demonstrated a capacity to induce durable remission, restore organ function, and improve survival rates, coupled with a reassuring safety profile. However, the field must still address issues of product standardization and long-term safety evaluation. Next-generation solutions-featuring engineered MSCs, iPSC-MSCs products, and vesicle-based therapies-hold the potential to usher in a new era of personalized SLE treatment. The conduct of large-scale randomized controlled trials is now imperative to definitively establish therapeutic efficacy and optimize clinical protocols.
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.