Evidence map›Paper›PMID 36894763›Full record

ReviewIntensive care medicine experimental2023

Bioengineered extracellular vesicles: future of precision medicine for sepsis.

Aina Areny-Balagueró, Anna Solé-Porta, Marta Camprubí-Rimblas, Elena Campaña-Duel, Adrián Ceccato, Anna Roig, Daniel Closa, Antonio Artigas

Open access · goldAbstract readReview
In one paragraph

Review in Intensive care medicine experimental, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 26% of its field
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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. 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

8 authors at 5 institutions in 1 country.

Aina Areny-Balagueró *Institut d'Investigació i Innovació Parc Taulí (I3PT), Parc Taulí Hospital Universitari, 08208, Sabadell, Spain. aareny@tauli.cat.ORCID http://orcid.org/0000-0001-9611-1781
Anna Solé-Porta *Institut de Ciència de Materials de Barcelona, ICMAB-CSIC, Campus UAB, 08193, Bellaterra, Spain. asole@icmab.es.
Marta Camprubí-RimblasInstitut d'Investigació i Innovació Parc Taulí (I3PT), Parc Taulí Hospital Universitari, 08208, Sabadell, Spain.ORCID https://orcid.org/0000-0002-4085-5324
Elena Campaña-DuelInstitut d'Investigació i Innovació Parc Taulí (I3PT), Parc Taulí Hospital Universitari, 08208, Sabadell, Spain.
Adrián CeccatoInstitut d'Investigació i Innovació Parc Taulí (I3PT), Parc Taulí Hospital Universitari, 08208, Sabadell, Spain.ORCID https://orcid.org/0000-0001-9454-062X
Anna RoigInstitut de Ciència de Materials de Barcelona, ICMAB-CSIC, Campus UAB, 08193, Bellaterra, Spain.ORCID https://orcid.org/0000-0001-6464-7573
Daniel ClosaInstitut d'Investigacions Biomèdiques de Barcelona, Consejo Superior de Investigaciones Científicas (IIBB-CSIC), 08036, Barcelona, Spain.ORCID https://orcid.org/0000-0003-3797-3095
Antonio ArtigasInstitut d'Investigació i Innovació Parc Taulí (I3PT), Parc Taulí Hospital Universitari, 08208, Sabadell, Spain.ORCID https://orcid.org/0000-0002-8029-1017
Universitat Autònoma de Barcelona · ESInstitut de Ciència de Materials de Barcelona · ESCentro de Investigación Biomédica en Red de Enfermedades Respiratorias · ESConsejo Superior de Investigaciones Científicas · ESCorporació Sanitària Parc Taulí · ES

Funding

Fundación Ramón Areces CIVP19S8207Instituto de Salud Carlos III PI18/00677
6 · The paper itself

Abstract

Sepsis is a syndromic response to infection and is frequently a final common pathway to death from many infectious diseases worldwide. The complexity and high heterogeneity of sepsis hinder the possibility to treat all patients with the same protocol, requiring personalized management. The versatility of extracellular vesicles (EVs) and their contribution to sepsis progression bring along promises for one-to-one tailoring sepsis treatment and diagnosis. In this article, we critically review the endogenous role of EVs in sepsis progression and how current advancements have improved EVs-based therapies toward their translational future clinical application, with innovative strategies to enhance EVs effect. More complex approaches, including hybrid and fully synthetic nanocarriers that mimic EVs, are also discussed. Several pre-clinical and clinical studies are examined through the review to offer a general outlook of the current and future perspectives of EV-based sepsis diagnosis and treatment.

Identifiers

PMID36894763
PMCPMC9998145
OpenAlexW4323655503

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.