Evidence map›Paper›PMID 41732236›Full record

ReviewJournal of translational autoimmunity2026

Extracellular vesicles and their role in Lupus Nephritis: A scoping review.

Lady J Rios-Serna, María Del Mar Rojas-Pelaez, Mildrey Mosquera Escudero, Herney Andres García-Perdomo, Carlos A Cañas

Abstract readReview
In one paragraph

Review in Journal of translational autoimmunity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Lady J Rios-SernaUniversidad Icesi, CIRAT: Centro de Investigación en Reumatología, Autoinmunidad y Medicina Traslacional, Cali, Colombia.
María Del Mar Rojas-PelaezUniversidad Icesi, CIRAT: Centro de Investigación en Reumatología, Autoinmunidad y Medicina Traslacional, Cali, Colombia.
Mildrey Mosquera EscuderoGrupo de Nutrición, Departamento de Ciencias Fisiológicas, Universidad Del Valle, Cali, Colombia.
Herney Andres García-PerdomoDivsion of Urology/Urooncology. Department of Surgery, School of Medicine, Universidad Del Valle, Cali, Colombia.
Carlos A CañasUniversidad Icesi, CIRAT: Centro de Investigación en Reumatología, Autoinmunidad y Medicina Traslacional, Cali, Colombia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lupus nephritis (LN) is one of the most severe and common complications of systemic lupus erythematosus (SLE), which pathogenesis is mainly driven by immune complex deposition and infiltration of immune cells, ultimately leading to progressive renal damage. Extracellular vesicles (EVs) are nanometer-sized particles released by almost all cell types that mediate intercellular communication and modulate diverse biological processes, including immune activation, through the transfer of vesicular cargo. Increasing evidence shows that EVs contribute significantly to the pathogenesis of LN, mediating processes such as antigen presentation, stimulating inflammatory cytokine production and facilitating immune complex deposition, among other mechanisms. Following this line of thought, EVs represent a promising source of specific biomarkers for early diagnosis, monitoring of disease activity and even development of therapeutic targets. This review focuses on summarizing the most recent findings on the role of EVs in LN pathophysiology, diagnosis, monitoring, and their potential for the development of therapeutic solutions.

Indexed as

BiomarkersExosomeKidneyPathophysiologySystemic lupus erythematosus

Identifiers

PMID41732236
PMCPMC12925574

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.