Evidence map›Paper›PMID 41354853›Full record

ArticleScientific reports2025

PLGA nanoparticles for oral delivery of prion-specific antigen: a novel approach to chronic wasting disease vaccination.

Mohamed M Elsutohy, Dalia Abdelaziz, Chimoné S Dalton, Byron Kruger, Shirley Phan, Yo-Ching Cheng, Kevin Low, Hanaa Ahmed-Hassan, Hermann M Schätzl

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Mohamed M ElsutohyCalgary Prion Research Unit, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, T2N 4Z6, Canada.
Dalia AbdelazizCalgary Prion Research Unit, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, T2N 4Z6, Canada.
Chimoné S DaltonCalgary Prion Research Unit, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, T2N 4Z6, Canada.
Byron KrugerCalgary Prion Research Unit, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, T2N 4Z6, Canada.
Shirley PhanCalgary Prion Research Unit, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, T2N 4Z6, Canada.
Yo-Ching ChengCalgary Prion Research Unit, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, T2N 4Z6, Canada.
Kevin LowCalgary Prion Research Unit, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, T2N 4Z6, Canada.
Hanaa Ahmed-HassanCalgary Prion Research Unit, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, T2N 4Z6, Canada.
Hermann M SchätzlCalgary Prion Research Unit, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, T2N 4Z6, Canada. hschaetz@ucalgary.ca.

Funding

Chronic Wasting Disease VaccinesR01AI156037 · NIAID · COLORADO STATE UNIVERSITY · PI MATHIASON, CANDACE K. · 2021 to 2025
$3.5M
Alberta Innovates 201600023; 222300851National Institute for Health Care Management Foundation R01AI156037Natural Sciences and Engineering Research Council of Canada Alliance Grant ALLRP 571218-21NIAID NIH HHS R01 AI156037
6 · The paper itself

Abstract

Prion diseases, such as chronic wasting disease (CWD), are incurable, fatal neurodegenerative disorders. We have developed a recombinant dimeric deer prion protein (Ddi) vaccine against CWD that has shown promising immune responses when injected subcutaneously (s.c). While s.c injection is suitable for controlled conditions, oral administration is practical in wildlife. Herein, we have developed an oral vaccine utilizing poly lactic co-glycolic acid (PLGA) nanoparticles, co-encapsulating Ddi and oligodeoxynucleotide adjuvant (CpG) using double emulsion-solvent evaporation technique. Our results showed production of spherical PLGA nanoparticles with size of ~ 200–300 nm, an acceptable surface charge (− 14.2 ± 5.73 mV), and an encapsulation efficiency of approximately 70 and 30%, for Ddi and CpG, respectively. We administered the developed vaccine to FVB mice orally and subcutaneously, followed by ELISA assays of the sera and feces. Mice receiving the vaccine subcutaneously exhibited high antibody reactivities to the used antigen in their sera (100% positivity), with no detectable positive reactivity in their feces. However, those receiving the oral vaccine showed 60 and 80% positivity in sera and feces, respectively, indicating specific mucosal immunity. We also found specific T cell reactivity in mice immunized orally. This approach is paving the way for developing an oral vaccine against CWD.

Indexed as

AntigensNanoparticlesPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPrionsWasting Disease, ChronicAdministration, OralAnimalsDeerFemaleMiceNanovaccinesProtein Subunit VaccinesVaccinationAntigensNanovaccinesPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPrionsProtein Subunit VaccinesChronic wasting diseaseNanovaccinesOral vaccinePLGA nanoparticlePrionPrion diseasesPrion vaccine

Identifiers

PMID41354853
PMCPMC12795844

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.