Evidence mapPaperPMID 42536162Full record

ReviewInflammation research : official journal of the European Histamine Research Society ... [et al.]2026

Effect of gut bacterial extracellular vesicles on angiogenic potential and vascular integrity: positive and negative aspects.

Sara Aghakhani Chegeni, Banafsheh Yalameha, Somayyeh Rashidi, Gonja Javani, Narjes Seddighi, Hesam Saghaei Bagheri, Masoud Khalifezadeh, Golbarg Roozbahani, Sara Molaaghaee-Rouzbahani, Reza Rahbarghazi

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In one paragraph

Review in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Sara Aghakhani ChegeniStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Banafsheh YalamehaStem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Somayyeh RashidiStem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Gonja JavaniNeurosciences Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Narjes SeddighiStem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Hesam Saghaei BagheriStem Cell and Regenerative Medicine Institute (SCARM), Tabriz University of Medical Sciences, Tabriz, Iran.
Masoud KhalifezadehStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Golbarg RoozbahaniApplied Cell Sciences Division, Department of Hematology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Sara Molaaghaee-RouzbahaniStem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Reza RahbarghaziStem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. rezarahbardvm@gmail.com.

Funding

Tabriz University of Medical Sciences IR.TBZMED.VCR.REC.1404.100
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are intercellular mediators in prokaryotic and eukaryotic systems that have the potential to regulate various physiological and pathological processes in recipient cells. Among them, bacterial extracellular vesicles (BEVs), including Gram-negative outer membrane vesicles (OMVs) and Gram-positive membrane vesicles (MVs) produced by the gut microbiota, have special roles in humans and animals. Due to their nanoscale dimensions and distinct molecular payloads, BEVs can cross biological barriers, including the vascular endothelium, to reach distant target tissues and affect various pathophysiological processes. Dysbiosis and compromised epithelial barriers facilitate the systemic dissemination of gut microbiota-derived BEVs, increasing the risk of diseases such as atherosclerosis and cardiovascular disease. Importantly, while this review emphasizes symbiotic intestinal BEVs, evidence from oral and pathogenic bacteria has also been integrated as indirect mechanistic sources to shed more light on BEV-induced endothelial dysfunction and altered angiogenesis. Here, we aimed to highlight the impact of BEVs on the vascular compartment, focusing on endothelial cells (ECs) in terms of molecular and cellular events. Understanding the underlying mechanisms will enable us to develop sophisticated engineered BEVs to control and inhibit certain pathological conditions.

Indexed as

AngiogenesisBacteriaExtracellular VesiclesGastrointestinal MicrobiomeAnimalsEndothelial CellsEndothelium, VascularHumansNeovascularization, PhysiologicAngiogenesisBacterial extracellular vesiclesGastrointestinal microbiomeVascular diseases

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.