Evidence map›Paper›PMID 42903459›Full record

ArticleJournal of parasitology research2026

In Silico Design and Immunogenicity Evaluation of a Multiepitope Vaccine Candidate Against

Sara Idriss, Almoutassem Billah Zetoune, Chadi Soukkarieh

Abstract read
In one paragraph

Article in Journal of parasitology research, 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

3 authors.

Sara IdrissDepartment of Biochemistry and Microbiology Faculty of Pharmacy Damascus University Damascus Syria damascusuniversity.edu.sy.ORCID https://orcid.org/0009-0005-6360-7787
Almoutassem Billah ZetouneDepartment of Biochemistry and Microbiology Faculty of Pharmacy Damascus University Damascus Syria damascusuniversity.edu.sy.ORCID https://orcid.org/0009-0009-7455-4093
Chadi SoukkariehDepartment of Animal Biology Faculty of Science Damascus University Damascus Syria damascusuniversity.edu.sy.ORCID https://orcid.org/0000-0002-7341-4277

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Cutaneous leishmaniasis caused by Methods: In this study, a MEV candidate was designed using conserved cytotoxic T lymphocyte (CTL), helper T lymphocyte (HTL), and linear B-cell epitopes derived from immunodominant Results: Computational analysis demonstrated stable interaction between the vaccine candidate and the TLR4 receptor. MD simulations confirmed the formation of a stable and compact vaccine-TLR4 complex, supported by RMSD, Rg, and PCA analyses, indicating reduced conformational fluctuations and enhanced receptor stabilization compared with the unbound state. Immunological analysis revealed a strong Th1-skewed immune response characterized by significant upregulation of IFN- Conclusion: Overall, the MEV induced coordinated cellular immune responses together with antigen-specific antibody recognition. The observed cytokine gene expression profile and antibody reactivity indicate a robust immunogenic response and support the recombinant construct as a promising candidate for further preclinical evaluation against cutaneous leishmaniasis. Additional studies assessing protective efficacy, parasite burden, and long-term immune durability are warranted.

Indexed as

BALB/c micecutaneous leishmaniasisLeishmania tropicamultiepitope vaccinerecombinant proteinTh1 response

Identifiers

PMID42903459
PMCPMC13680856

What OpenQuestion holds

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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.