Evidence map›Paper›PMID 38844736›Full record

ArticleJournal of extracellular vesicles2024

Amniotic fluid stem cell-derived extracellular vesicles educate type 2 conventional dendritic cells to rescue autoimmune disorders in a multiple sclerosis mouse model.

Giorgia Manni, Marco Gargaro, Doriana Ricciuti, Simona Fontana, Eleonora Padiglioni, Marco Cipolloni, Tommaso Mazza, Jessica Rosati, Alessandra di Veroli, Giulia Mencarelli and 13 more

Abstract read
In one paragraph

Article in Journal of extracellular vesicles, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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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

23 authors.

Giorgia ManniDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.ORCID https://orcid.org/0000-0002-5697-2648
Marco GargaroDepartment of Pharmaceutical Science, University of Perugia, Perugia, Italy.
Doriana RicciutiDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Simona FontanaDepartment of Biomedicine, Neurosciences and advanced Diagnostics (Bi.N.D) School of Medicine, University of Palermo, Palermo, Italy.ORCID https://orcid.org/0000-0003-4681-2170
Eleonora PadiglioniDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Marco CipolloniTES Pharma Srl, I, Corciano, Perugia, Italy.
Tommaso MazzaBioinformatics unit, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.
Jessica RosatiCellular Reprogramming Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.
Alessandra di VeroliDepartment of Chemistry, Biology and Biotechnology, University of Perugia, Perugia, Italy.
Giulia MencarelliDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Benedetta PieroniDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Estevão Carlos Silva BarcelosDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Giulia ScalisiDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Francesco SarnariDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Alessandro di MicheleExtracellular Vesicles network (EV-net) of the University of Perugia, Perugia, Italy.
Luisa PascucciExtracellular Vesicles network (EV-net) of the University of Perugia, Perugia, Italy.
Francesca de FrancoTES Pharma Srl, I, Corciano, Perugia, Italy.
Teresa ZelanteDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Cinzia AntognelliDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Gabriele CrucianiDepartment of Chemistry, Biology and Biotechnology, University of Perugia, Perugia, Italy.
Vincenzo Nicola TalesaDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Rita RomaniDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Francesca FallarinoDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.

Funding

Associazione Italiana per la Ricerca sul Cancro AIRC 19903Fondazione Italiana Sclerosi Multipla FISM 2019/R-single/012Fondazione Telethon GMR22T1081H2020 European Research Council 101078646H2020 European Research Council ERCH2020 European Research Council REACT-DCNextGenerationEU under the Italian MUR Vitality National Innovation Ecosystem grant ECS00000041PRIN Prin 2017BZEREZUniversity of Perugia Azione di Ateneo 2022 "Regenia" to FF
6 · The paper itself

Abstract

Dendritic cells (DCs) are essential orchestrators of immune responses and represent potential targets for immunomodulation in autoimmune diseases. Human amniotic fluid secretome is abundant in immunoregulatory factors, with extracellular vesicles (EVs) being a significant component. However, the impact of these EVs on dendritic cells subsets remain unexplored. In this study, we investigated the interaction between highly purified dendritic cell subsets and EVs derived from amniotic fluid stem cell lines (HAFSC-EVs). Our results suggest that HAFSC-EVs are preferentially taken up by conventional dendritic cell type 2 (cDC2) through CD29 receptor-mediated internalization, resulting in a tolerogenic DC phenotype characterized by reduced expression and production of pro-inflammatory mediators. Furthermore, treatment of cDC2 cells with HAFSC-EVs in coculture systems resulted in a higher proportion of T cells expressing the regulatory T cell marker Foxp3 compared to vehicle-treated control cells. Moreover, transfer of HAFSC-EV-treated cDC2s into an EAE mouse model resulted in the suppression of autoimmune responses and clinical improvement. These results suggest that HAFSC-EVs may serve as a promising tool for reprogramming inflammatory cDC2s towards a tolerogenic phenotype and for controlling autoimmune responses in the central nervous system, representing a potential platform for the study of the effects of EVs in DC subsets.

Indexed as

Amniotic FluidDendritic CellsDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalExtracellular VesiclesMultiple SclerosisAnimalsFemaleHumansMiceMice, Inbred C57BLStem Cellsamniotic fluid stem cellsautoimmune diseasesconventional dendritic cell type 2 (cDC2)dendritic cellsexperimental autoimmune encephalomyelitis (EAE)extracellular vesiclestolerogenic phenotype

Identifiers

PMID38844736
PMCPMC11156524

What Socratic 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 Socratic graph.