Evidence map›Paper›PMID 41463825›Full record

ArticleAnimals : an open access journal from MDPI2025

Inactivated Type 'O' Foot and Mouth Disease Virus Encapsulated in Chitosan Nanoparticles Induced Protective Immune Response in Guinea Pigs.

Kalaivanan Ramya, Subodh Kishore, Palanisamy Sankar, Ganesh Kondabatulla, Bedaso Mamo Edao, Ramasamy Saravanan, Kumaraguruban Karthik

Abstract read
In one paragraph

Article in Animals : an open access journal from MDPI, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Kalaivanan RamyaIndian Veterinary Research Institute, Hebbal, Bangalore 560024, India.ORCID 0000-0001-5853-1638
Subodh KishoreIndian Veterinary Research Institute, Hebbal, Bangalore 560024, India.
Palanisamy SankarVeterinary College and Research Institute, Tamil Nadu Veterinary and Animal Sciences University, Udumalpet 642205, India.
Ganesh KondabatullaIndian Veterinary Research Institute, Hebbal, Bangalore 560024, India.ORCID 0000-0002-2305-1797
Bedaso Mamo EdaoIndian Veterinary Research Institute, Hebbal, Bangalore 560024, India.
Ramasamy SaravananVeterinary College and Research Institute, Tamil Nadu Veterinary and Animal Sciences University, Namakkal 637002, India.ORCID 0000-0003-2409-0357
Kumaraguruban KarthikVeterinary College and Research Institute, Tamil Nadu Veterinary and Animal Sciences University, Udumalpet 642205, India.ORCID 0000-0002-9215-6306

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Foot and mouth disease is a contagious viral disease infecting ungulates, with great economic impact on farmers' income; it is primarily controlled using inactivated vaccines, which have certain limitations, such as short-lived immunity and a lack of mucosal immunity at the portals of virus entry. The present approach aims to exploit the efficiency of chitosan nanoparticle-encapsulated inactivated type 'O' FMDV antigen (FMDV-CS-NPs) to induce mucosal and systemic immune responses in a guinea pig animal model through intranasal and intramuscular administration in comparison with the conventional inactivated, mineral oil-adjuvanted vaccine that is administered systemically. In this study, the FMDV-CS-NPs were prepared by ionotropic gelation, followed by incubation; were characterized for their physical properties and in vitro antigen release; and were found to encapsulate a good amount of antigen. The prepared nanoparticles were assessed for their ability to induce humoral and cell-mediated immune responses by SNTs; indirect ELISAs for serum IgG, IgG1, and IgG2; and nasal washing sIgA and lymphocyte proliferation assays. The preparation induced comparatively more measurable sIgA and systemic immune responses with the intranasal and intramuscular routes of administration, respectively, which are attributable to a specific interaction between the positively charged chitosan and the negatively charged mucosal surface and cell membrane. The challenge infection protected 87.5% of the animals in the FMDV-CS-NP I/M group, followed by 77.7% in the FMDV-CS-NP I/N and inactivated vaccine groups. The outcomes of this study in guinea pigs highlight that chitosan nanoparticle-based vaccine formulations could be employed as a promising antigen delivery system for targeted delivery, devoid of any adverse effect, to induce protective immune responses.

Indexed as

chitosanFMDVguinea pigimmune responsenanoparticlesprotectionroute of immunization

Identifiers

PMID41463825
PMCPMC12729774

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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.