ArticleActa parasitologica2025
Design of a Multi-epitope Antigen for Toxoplasmosis Diagnosis: An Immunoinformatics Approach.
Article in Acta parasitologica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- A comprehensive multi-epitope recombinant protein strategy for accurate serological detection of Toxoplasma gondii infection.Medical microbiology and immunology · 2025Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
Toxoplasma gondii, as an obligatory intracellular protozoan, can infect a diverse array of individuals and warm-blooded creatures. Considering the worldwide public health implications caused by T. gondii infection, it is an important goal to develop effective diagnostic tests or vaccines. The application of natural antigens derived from the parasite in these assessments encounters challenges, including the complexities of culturing the parasites, strain differences, and the high cost of kits produced based on natural antigens. The current bioinformatic study aimed to develop a multi-epitope T. gondii protein based on various immunoinformatic web servers to improve serodiagnosis. The linear and conformational B-cell epitope prediction of Surface Antigens 1(SAG1) and 2(SAG2), Dense granule proteins 2 (GRA2), 6 (GRA6), and 7 (GRA7), was conducted by the ABCpred and BepiPred servers, respectively. A variety of web servers were then accessed to predict antigenicity, solubility, and physicochemical properties, as well as to analyze secondary and tertiary structures, refine the 3D model, and validate the findings. Consequently, conformational B-cell epitopes were identified to explore potential protein-antibody interactions. In conclusion, further experimental evaluation is necessary for this multi-epitope construct for its subsequent incorporation in commercial serodiagnostic kits.
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Registered trials
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.