Evidence map›Paper›PMID 35769256›Full record

ArticleFrontiers in cell and developmental biology2022

Lipidic Profile Changes in Exosomes and Microvesicles Derived From Plasma of Monoclonal Antibody-Treated Psoriatic Patients.

Giovanni Paolino, Sandra Buratta, Santo R Mercuri, Roberto M Pellegrino, Lorena Urbanelli, Carla Emiliani, Lucia Bertuccini, Francesca Iosi, Veronica Huber, Pina Brianti and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 37 citations in OpenAlex.

  1. The relevance of membrane lipid composition in exosome-based precision dermatology.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
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  17. Pharmaco-Omics in Psoriasis: Paving the Way towards Personalized Medicine.International journal of molecular sciences · 2023
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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

14 authors at 2 institutions in 1 country.

Giovanni PaolinoUnit of Dermatology and Cosmetology, San Raffaele Hospital, Milan, Italy.
Sandra BurattaDepartment of Chemistry, Biology and Biotechnology, University of Perugia, Perugia, Italy.
Santo R MercuriUnit of Dermatology and Cosmetology, San Raffaele Hospital, Milan, Italy.
Roberto M PellegrinoDepartment of Chemistry, Biology and Biotechnology, University of Perugia, Perugia, Italy.
Lorena UrbanelliDepartment of Chemistry, Biology and Biotechnology, University of Perugia, Perugia, Italy.
Carla EmilianiDepartment of Chemistry, Biology and Biotechnology, University of Perugia, Perugia, Italy.
Lucia BertucciniCore Facilities, Microscopy Unit, Istituto Superiore di Sanità, Rome, Italy.
Francesca IosiCore Facilities, Microscopy Unit, Istituto Superiore di Sanità, Rome, Italy.
Veronica HuberUnit of Immunotherapy of Human Tumors, National Institute of Tumors, Milan, Italy.
Pina BriantiUnit of Dermatology and Cosmetology, San Raffaele Hospital, Milan, Italy.
Caterina PreziosoUnit of Dermatology and Cosmetology, San Raffaele Hospital, Milan, Italy.
Matteo R Di NicolaUnit of Dermatology and Cosmetology, San Raffaele Hospital, Milan, Italy.
Cristina FedericiDepartment of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.
Luana LuginiDepartment of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.
Istituto Superiore di Sanità · ITUniversity of Perugia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Psoriasis is a chronic immune-mediated inflammatory skin disorder affecting children and adults. To date no approved biomarkers for diagnosis of this disease and follow up of patients have been translated into clinical practice. Recently, extracellular vesicles (EVs) secreted by all cells and present in almost all biological fluids are playing a crucial role in diagnosis and follow up of several diseases, including psoriasis. Since many psoriatic patients show altered plasma lipid profiles and since EVs have been involved in psoriasis pathogenesis, we studied the phospholipid profile of EVs, both microvesicles (MV) or exosomes (Exo), derived from plasma of psoriatic patients undergoing systemic biological treatment (secukinumab, ustekinumab, adalimumab), in comparison with EVs of untreated patients and healthy donors (HD). EVs were evaluated by immune electronmicroscopy for their morphology and by NanoSight for their amount and dimensions. EV phospholipid profiling was performed by High Resolution Liquid Chromatography-Mass Spectrometry and statistical Partial Least Squares Discriminant Analysis. Our results demonstrated that psoriatic patients showed a higher concentration of both MV and Exo in comparison to EVs from HD. The phospholipid profile of Exo from psoriatic patients showed increased levels of phosphatidylcholine (PC), phosphatidylethanolamine (PE), phosphatidylglycerol and lysoPC compared to Exo from HD. Sphingomyelin (SM) and phosphatidylinositol (PI) are the only phospholipid classes whose levels changed in MV. Moreover, the therapy with ustekinumab seemed to revert the PE and PC lipid composition of circulating Exo towards that of HD and it is the only one of the three biological drugs that did not alter SM expression in MV. Therefore, the determination of lipid alterations of circulating EVs could harbor useful information for the diagnosis and drug response in psoriatic patients.

Indexed as

exosomesinflammatory skin diseaseslipidic profilemicrovesciclesmonoclonal antibody treatmentpsoriasis

Identifiers

PMID35769256
PMCPMC9234320
OpenAlexW4282588205

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Registered trials

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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.