Evidence map›Paper›PMID 41878131›Full record

ArticleInternational journal of nanomedicine2026

Antigen-Containing Silk Nanoparticles: A New Potential as Oral Vaccine Carriers.

Mitsuru Sato, Chisato Sakuma, Hideki Sezutsu, Katsura Kojima

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

4 authors.

Mitsuru Sato *Silkworm Research Group, Division of Silk-Producing Insect Biotechnology, Institute of Agrobiological Sciences, National Agriculture and Food Research Organization, Tsukuba, Ibaraki, 305-8634, Japan.ORCID 0009-0001-6688-836X
Chisato SakumaSilkworm Research Group, Division of Silk-Producing Insect Biotechnology, Institute of Agrobiological Sciences, National Agriculture and Food Research Organization, Tsukuba, Ibaraki, 305-8634, Japan.
Hideki SezutsuSilkworm Research Group, Division of Silk-Producing Insect Biotechnology, Institute of Agrobiological Sciences, National Agriculture and Food Research Organization, Tsukuba, Ibaraki, 305-8634, Japan.
Katsura Kojima *Silk Materials Research Group, Division of Silk-Producing Insect Biotechnology, Institute of Agrobiological Sciences, National Agriculture and Food Research Organization, Tsukuba, Ibaraki, 305-8634, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Oral vaccines are safer, easier to administer, and more cost-effective than injectable vaccines are. They induce systemic and mucosal immunity, thereby providing broad protection. However, developing an orally administered vaccine that can traverse the stomach and safely reach the intestinal tract to induce antigen-specific immune responses is challenging. Recently, many effective nanoparticle (NP) drug delivery systems have been developed. Various polymeric materials, including synthetic biodegradable and natural polymers, have been used as drug delivery matrices. Silk fibroin, a natural polymer, shows promise as a suitable material for drug delivery due to its biocompatibility, biodegradability, and aqueous processability. In this study, to investigate the potential of silk proteins as oral vaccine carriers, we prepared ovalbumin (OVA)-containing silk NPs through salting-out an aqueous solution of degummed fibers and non-degummed cocoons obtained from silkworms ( Methods: For the OVA-containing silk NPs, OVA was prepared through salting-out a mixture of OVA and an aqueous solution of cocoons or degummed fibers. OVA-specific antibody production in mice orally administrated OVA-containing silk NPs was analyzed using ELISA. Silk NP delivery to the intestinal tract of mice was monitoring using FITC-incorporated silk. The FITC-labeled cocoon and degummed fiber NPs were incubated with peritoneal macrophages, and their internalization observed using fluorescence imaging. Results: OVA-containing silk NPs can be delivered to the intestinal tract after oral administration to mice and subsequently induce OVA-specific serum IgG and intestinal IgA production without the need for adjuvants. Moreover, internalization of FITC-labeled cocoon or degummed fiber NPs into peritoneal macrophages was observed in vitro. Conclusion: Overall, silk NPs are promising oral vaccine carriers that can deliver antigens to the intestinal tract while avoiding decomposition by gastric acid and digestive enzymes, thereby facilitating the activation of mucosal and systemic immunity.

Indexed as

AntigensDrug CarriersFibroinsNanoparticlesOvalbuminSilkVaccinesAdministration, OralAnimalsBombyxFemaleMiceMice, Inbred BALB CNanovaccinesAntigensDrug CarriersFibroinsNanovaccinesOvalbuminSilkVaccinesantibody productionfibroinsnanoparticles-based drug delivery systemoral administration

Identifiers

PMID41878131
PMCPMC13007965

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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.