Evidence map›Paper›PMID 41751016›Full record

ArticleAnimals : an open access journal from MDPI2026

EgLDH as a Novel Target: Design and Preliminary Efficacy Assessment of a DNA Vaccine.

Jianan Zhao, Wenqing Zhao, Na Pu, Xuke Chen, Jiaxin Zhao, Juncheng Huang, Yanyan Zhang, Yan Sun, Xinwen Bo, Zhengrong Wang

Abstract read
In one paragraph

Article in Animals : an open access journal from MDPI, 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

10 authors.

Jianan ZhaoCollege of Animal Science and Technology, Shihezi University, Shihezi 832000, China.
Wenqing ZhaoCollege of Animal Science and Technology, Shihezi University, Shihezi 832000, China.
Na PuCollege of Animal Science and Technology, Shihezi University, Shihezi 832000, China.
Xuke ChenCollege of Animal Science and Technology, Shihezi University, Shihezi 832000, China.
Jiaxin ZhaoCollege of Animal Science and Technology, Shihezi University, Shihezi 832000, China.
Juncheng HuangCollege of Animal Science and Technology, Shihezi University, Shihezi 832000, China.
Yanyan ZhangCollege of Animal Science and Technology, Shihezi University, Shihezi 832000, China.
Yan SunCollege of Animal Science and Technology, Shihezi University, Shihezi 832000, China.
Xinwen BoCollege of Animal Science and Technology, Shihezi University, Shihezi 832000, China.
Zhengrong WangCollege of Animal Science and Technology, Shihezi University, Shihezi 832000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

(1) Background: Echinococcosis is a significant zoonotic disease that the World Health Organization (WHO) aims to eliminate by 2050. Current drug-based control faces challenges such as drug resistance, highlighting the urgent need to develop vaccines as a supplementary strategy. Although some progress has been made in the study of intermediate host vaccines using antigens such as Eg95, there is still no commercial vaccine available for the definitive host, canines-which are crucial for transmission-and it is not yet suitable for large-scale use. While vaccine studies targeting the key enzyme lactate dehydrogenase (LDH) in parasite energy metabolism remain scarce, they represent a promising area of potential. (2) Methods: The B cell antigen epitopes of LDH were analyzed, and prokaryotic (pET-28a-EgLDH) and eukaryotic (pVAX1-EgLDH) DNA vaccine expression vectors were constructed. After verifying expression and immunogenicity via qRT-PCR and WB, in vitro validation was performed in 293T cells. Mice were immunized with the vaccine and then challenged with the parasite; blood was collected from the orbital sinus, and IgG levels and cytokines were measured by ELISA. Protective effects were assessed through counting liver cysts and histopathological analysis. (3) Results: We constructed the pVAX1-EgLDH plasmid and immunized Kunming (KM) mice. Compared with the PBS control group, the vaccine group showed an 80.95% reduction in liver cysts (Quil-A group: 19.00%). Histopathological analysis indicated no significant liver damage, although the spleens in the vaccine group were smaller. ELISA results demonstrated an increase in total IgG (

Indexed as

Cystic EchinococcosisDNA vaccinesEgLDH

Identifiers

PMID41751016
PMCPMC12937295

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.