Evidence map›Paper›PMID 41716171›Full record

ReviewVeterinary world2025

Chitosan nanoparticles as next-generation carriers for veterinary DNA vaccines: Mechanisms, immune responses, and translational prospects.

Miguel González-Lozano, José Alberto Cano-Buendía

Abstract readReview
In one paragraph

Review in Veterinary world, 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. 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

2 authors.

Miguel González-LozanoFacultad de Medicina Veterinaria y Zootecnia; Center for Teaching, Research and Extension in Swine Production, Universidad Nacional Autónoma de Mexico (UNAM), Cuidad Universitaria, 04510; Mexico City, Mexico.
José Alberto Cano-BuendíaFacultad de Medicina Veterinaria y Zootecnia; Department of Microbiology and Immunology, Universidad Nacional Autónoma de Mexico (UNAM), Cuidad Universitaria, 04510; Mexico City, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chitosan-based DNA nanoparticles have emerged as a promising next-generation platform for veterinary vaccines, addressing several limitations of conventional attenuated, inactivated, and recombinant formulations. Chitosan is a biodegradable, biocompatible, and low toxicity polymer with mucoadhesive properties that enhance cellular uptake and protect nucleic acids from enzymatic degradation. These characteristics make it an attractive candidate for delivering plasmid DNA encoding viral antigens across diverse animal species. Recent advances demonstrate that chitosan-DNA nanoparticles can induce robust humoral and cellular immune responses, stimulate mucosal immunity, and achieve high levels of protection in terrestrial livestock, poultry, fish, and crustaceans. A wide range of viral pathogens has been targeted using this approach, including Foot-and-Mouth disease virus, Newcastle disease virus, infectious bronchitis virus, spring viremia of carp virus, white spot syndrome virus, and infectious pancreatic necrosis virus. Depending on the species and formulation strategy, nanoparticles have been successfully administered intranasally, intramuscularly, intraperitoneally, or orally, highlighting their versatility for mass vaccination in both terrestrial and aquatic systems. Reported protection rates range from 60% to 100% in mammalian and avian models, while oral nanoparticle vaccines in shrimp and fish have demonstrated sustained immune activation and survival benefits. The ability to incorporate genetic adjuvants, such as cytosine-phosphate-guanine motifs, cytokines, or complement fragments, further enhances the immunogenicity of these platforms. Despite these promising results, several challenges remain. Most studies use small laboratory animals or controlled experimental settings, and data from large-scale field trials in cattle, pigs, and equines remain scarce. The stability of nanoparticle formulations during long-term storage, the scalability of manufacturing processes, and the standardization of dosing regimens require further investigation. Overall, chitosan-DNA nanoparticles represent a safe, flexible, and rapidly adaptable vaccine carrier system with significant potential to transform veterinary immunization. Their capacity to elicit mucosal and systemic immunity, enable needle-free delivery, and support DIVA-compatible vaccine design positions them as a valuable tool for controlling emerging and re-emerging viral diseases in the context of One Health.

Indexed as

chitosan nanoparticlesgenetic immunizationmucosal vaccinationnanocarriersnanotechnology in animalsOne Healthplasmid DNAvaccine delivery systemsveterinary DNA vaccinesviral diseases

Identifiers

PMID41716171
PMCPMC12913849

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.