Evidence map›Paper›PMID 42751309›Full record

ArticleInternational journal of pharmaceutics: X2026

Immunostimulant-integrated acrylate nanocomposite adjuvants potentiate foot-and-mouth disease vaccine efficacy.

Lu Bai, Mingguang Hu, Haijun Zhou, Xiaoqi Chen, Fen Zhang, Yantao Li, Hua Cheng, Mengmeng Zhou

Abstract read
In one paragraph

Article in International journal of pharmaceutics: X, 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

8 authors.

Lu BaiInstitute of Energy Resources, Hebei Academy of Sciences, Shijiazhuang 050081, Hebei Province, China.
Mingguang HuInstitute of Energy Resources, Hebei Academy of Sciences, Shijiazhuang 050081, Hebei Province, China.
Haijun ZhouInstitute of Energy Resources, Hebei Academy of Sciences, Shijiazhuang 050081, Hebei Province, China.
Xiaoqi ChenInstitute of Energy Resources, Hebei Academy of Sciences, Shijiazhuang 050081, Hebei Province, China.
Fen ZhangInstitute of Energy Resources, Hebei Academy of Sciences, Shijiazhuang 050081, Hebei Province, China.
Yantao LiInstitute of Energy Resources, Hebei Academy of Sciences, Shijiazhuang 050081, Hebei Province, China.
Hua ChengInstitute of Biology, Hebei Academy of Sciences, Shijiazhuang 050081, Hebei Province, China.
Mengmeng ZhouHebei Key Laboratory of Pharmaceutical Polymer Excipients; Shijiazhuang Polymer Composite Technological Innovation Center, College of Chemical Engineering, Shijiazhuang University, Shijiazhuang 050035, Hebei Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Foot-and-mouth disease (FMD) is a viral infectious disease of artiodactyls that threatens the global livestock economy and public health security. Vaccination is employed to prevent the occurrence of infectious diseases, and adjuvants play a key role in vaccine preparation. Commercially available FMD vaccines mainly use oil-emulsion adjuvants that induce a humoral immune response in the body. Based on the acrylate hydrogel adjuvant (AHN) with sustained-release properties, this study introduced CpG, Poly I:C, and QS-21 immunostimulants to create an prepare immunostimulant-integrated acrylate nanocomposite adjuvant (AHN@X) combining excellent antigen delivery capability and immune response direction regulation for use in FMD vaccines. AHN@X has a particle size of less than 100 nm, and it exhibits good storage stability at 4 °C. The FMD vaccines prepared with AHN@X nanocomposite adjuvant were immunized by intramuscular injection in BALB/c mice. The results showed that it could efficiently induce specific IgG, IgG1 and IgG2a antibody titers and activate B cells and T cells. Moreover, AHN@C stimulated splenocytes to secrete cytokines IFN-γ and IL-4 at the highest concentrations, 58.34 pg/mL and 32.24 pg/mL respectively. Additionally, the AHN@C nanocomposite adjuvant promoted the strongest endocytosis of antigens by macrophages, and it efficiently induced humoral immune responses and cellular immune responses. Overall, the clinical protective efficacy of AHN@C against FMDV is worth subsequent validation in target livestock animals.

Indexed as

AcrylateFoot-and-mouth diseaseImmune responsesImmunological evaluationImmunostimulantNanocomposite adjuvants

Identifiers

PMID42751309
PMCPMC13579442

What OpenQuestion holds

Textmetadata
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.