Evidence map›Paper›PMID 39963417›Full record

ArticleInternational journal of nanomedicine2025

Biodegradable Electrospun PLGA Nanofibers-Encapsulated Trichinella Spiralis Antigens Protect from Relapsing Experimental Autoimmune Encephalomyelitis and Related Gut Microbiota Dysbiosis.

Ljiljana Sabljić, Nataša Radulović, Jelena Đokić, Dusica B Stojanovic, Dušan Radojević, Sofija Glamočlija, Miroslav Dinić, Nataša Golić, Saša Vasilev, Petar Uskoković and 3 more

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

13 authors.

Ljiljana SabljićInstitute for the Application of Nuclear Energy, University of Belgrade, Belgrade, Serbia.ORCID 0000-0001-6027-591X
Nataša RadulovićInstitute for Biological Research "Siniša Stanković", University of Belgrade, Belgrade, Serbia.
Jelena ĐokićInstitute for Molecular Genetics and Genetical Engineering, University of Belgrade, Belgrade, Serbia.
Dusica B StojanovicFaculty of Metallurgy and Technology, University of Belgrade, Belgrade, Serbia.ORCID 0000-0001-6308-7586
Dušan RadojevićInstitute for Molecular Genetics and Genetical Engineering, University of Belgrade, Belgrade, Serbia.
Sofija GlamočlijaInstitute for the Application of Nuclear Energy, University of Belgrade, Belgrade, Serbia.
Miroslav DinićInstitute for Molecular Genetics and Genetical Engineering, University of Belgrade, Belgrade, Serbia.
Nataša GolićInstitute for Molecular Genetics and Genetical Engineering, University of Belgrade, Belgrade, Serbia.
Saša VasilevInstitute for the Application of Nuclear Energy, University of Belgrade, Belgrade, Serbia.ORCID 0000-0001-7870-2713
Petar UskokovićFaculty of Metallurgy and Technology, University of Belgrade, Belgrade, Serbia.
Ljiljana Sofronić-MilosavljevićInstitute for the Application of Nuclear Energy, University of Belgrade, Belgrade, Serbia.
Alisa Gruden-Movsesijan *Institute for the Application of Nuclear Energy, University of Belgrade, Belgrade, Serbia.
Sergej Tomić *Institute for the Application of Nuclear Energy, University of Belgrade, Belgrade, Serbia.ORCID 0000-0003-2570-1295

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Methods: To test this, we encapsulated ESL1 antigens into biodegradable poly (lactide-co-glycolic) acid (PLGA) nanofibers by emulsion electrospinning as a delivery system and assessed their release dynamics in vitro, and in an animal MS model, experimental autoimmune encephalomyelitis (EAE), induced 7 days after PLGA/ESL1 subcutaneous implantation. PLGA/ESL1 effects on EAE symptoms were monitored along with multiple immune cell subsets in target organs at the peak and recovery of EAE. Gut barrier function and microbiota composition were analyzed using qPCR, 16S rRNA sequencing, and metabolomic analyses. Results: ESL1 antigens, released from PLGA and drained via myeloid antigen-presenting cells through lymph nodes, protected the animals from developing EAE symptoms. These effects correlated with reduced activation of myeloid cells, increased IL-10 expression, and reduced accumulation of proinflammatory natural killer (NK) cells, T helper (Th)1 and Th17 cells in the spleen and central nervous system (CNS). Additionally, CD4 Conclusion: The delivery of

Indexed as

Antigens, HelminthDysbiosisEncephalomyelitis, Autoimmune, ExperimentalGastrointestinal MicrobiomeNanofibersPolylactic Acid-Polyglycolic Acid CopolymerTrichinella spiralisAnimalsFemaleMiceMice, Inbred C57BLAntigens, HelminthPolylactic Acid-Polyglycolic Acid Copolymerdrug deliveryelectrospinninggut microbiotaimmune modulationPLGA nanofiberstolerogenic cells

Identifiers

PMID39963417
PMCPMC11830953

What OpenQuestion holds

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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.